Rogeria creightoni

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Rogeria creightoni
Scientific classification
Kingdom: Animalia
Phylum: Arthropoda
Class: Insecta
Order: Hymenoptera
Family: Formicidae
Subfamily: Myrmicinae
Tribe: Solenopsidini
Genus: Rogeria
Species: R. creightoni
Binomial name
Rogeria creightoni
Snelling, R.R., 1973

Rogeria creightoni casent0003231 profile 1.jpg

Rogeria creightoni casent0003231 dorsal 1.jpg

Specimen labels

A common and widespread Rogeria species. The types were collected in a residential area that was formerly mesquite-acacia savannah. Other specimens come from riparian woodland, palm-thorn forest, rain forest, pine-oak forest, cecropia forest, and cacao plantation. Most were taken in leaf litter on the ground. Some Belize specimens were under a termite nest; another in orchids.


Kugler (1994) - creightoni species group. WL 0.63-0.93mm. Clypeal apron usually with weak to distinct median notch. Eyes small, oval to circular (EL/SpL 0.29-0.64). Metanotal groove weak or absent. MHI usually 0.90-1.06. Propodeal spines long (PSI usually > 0.17), often nearly horizontal. Postpetiolar node from above usually subtrapezoidal, sometimes subrectangular; anterior edge of sternum not prominent. Sides of head distinctly rugose-areolate. Pronotal disc transversely rugose-areolate on anterior edge and longitudinally rugose-areolate behind. Scapes and extensor surfaces of tibiae with erect-suberect hairs.

See nomenclature section below and Rogeria alzatei, Rogeria belti, Rogeria brunnea, and Rogeria cornuta.

Keys including this Species


Southern Texas to Costa Rica; from about 1,500m in parts of Chiapas and Costa Rica to sea level.

Latitudinal Distribution Pattern

Latitudinal Range: 28.33333° to 9.15°.

Tropical South

Distribution based on Regional Taxon Lists

Nearctic Region: United States (type locality).
Neotropical Region: Belize, Costa Rica, Guatemala, Honduras, Mexico.

Distribution based on AntMaps


Distribution based on AntWeb specimens

Check data from AntWeb


The following is modified from Kugler (1994): Little is known about these cryptic ants. Collection records typically range from sea level to 1000m, but five species extend higher and two (Rogeria unguispina and Rogeria merenbergiana) can be found at 2000m. Rogeria 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 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 species have only been collected as strays or by Berlese or Winkler sampling, from 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 the 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.

Nests are 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.


Queens have been collected in Costa Rica but remain undescribed; males have not been collected.


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

  • creightoni. Rogeria creightoni Snelling, R.R. 1973a: 2, fig. 1 (w.) U.S.A. See also: Kugler, C. 1994: 50.

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

Kugler (1994) - This species becomes quite heterogeneous with this revision. Ants from almost every locality are different from the others in some conspicuous way. Specimens from Belize have the longest propodeal spines (PSI 0.24-0.28), more prominent metapleural lobes, weak or absent petiolar keel and thicker ridges in macrosculpture. The Texas specimens have similar habitus, but have somewhat shorter propodeal spines (PSI 0.21-0.23), less prominent metapleural lobes, more distinct petiolar keel and less thickened macrosculpture. A Tamaulipas specimen is similar to the Texas specimens, but has longer, distinctly inclined propodeal spines. Specimens from Yucatán, and Chiapas are the largest (WL 0.78-0.93mm), have a prominent clypeal body, somewhat longer scapes, small circular eye, strong nuchal groove, relatively shorter propodeal spines (PSI 0.19-0.22), and head macrosculpture with sharp ridges and unusually large areolae. Specimens from La Selva, Costa Rica are similar, but have normal clypeus and sculpture. Others from Costa Rica have shorter, more inclined propodeal spines (PSI 0.16-0.20), a more distinct petiolar node and keel, and subrectangular postpetiolar node. One specimen from Oaxaca is more like those from Belize; another is more like the San Jose specimens. With little material from most localities, I did not feel confident naming a new species for each variant, but as collections improve, I will not be surprised if this species undergoes fission.

At one time during the revision I also considered describing Rogeria cornuta, Rogeria innotabilis,Rogeria leptonana, and Rogeria alzatei as variants of creightoni . But now I believe they can delineated. Comparison of creightoni with leptonana is found in key couplet 40; comparisons with cornuta and alzatei, in their respective discussions. All known specimens of innotabilis fall within the geographic range of creightoni and the two species are sympatric in at least one locality. All specimens of creightoni differ from innotabilis in several ways: 1) erect hair on scapes and tibiae, 2) palpal formula 3,2, 3) clypeal apron with weak to distinct median notch, and 4) postpetiolar sternum not prominent. The regional variants differ in additional, but inconsistent ways.

Kugler 1994 fig 49-54

A single queen from Trinidad (N. A. Weber #129) is very much like the three Costa Rican and Colombian queens provisionally assigned to innotabilis in size, general habitus, triangular mandibles, convex clypeus, robust mesosoma (MHI 1.28), propodeal spine size and shape, and subrectangular postpetiolar node, but differs in having erect hair on scapes and tibiae, little or no keel on petiolar peduncle, undulate ventral profile of postpetiole, and longitudinally oriented sculpture on the posterior head. On the basis of the pilosity, I provisionally assign the Trinidad queen to creightoni , but because of its great similarity in other respects to the innotabilis-like queens, and because neither set of queens is from an area where workers of creightoni or innotabilis have been collected, I do not feel confident of these assignments.



Kugler (1994) - TL 2.4-3.5, HL 0.58-0.81, HW 0.51-0.72, SL 0.38-0.55, EL 0.05-0.10 (8-16 facets), PW 0.37-0.52, WL 0.63-0.93, SpL 0.1 1-0.20, PetL 0.27-0.40, PpetL 0.14-0.22mm, CI 0.85-0.91, OI 0.08-0.17, SI 0.68-0.80, PSI 0.16-0.28, MHI 0.87-1.08. N=21

Mandibles with 5-7 teeth, if 5, may have 1-2 additional basal denticles. Basal tooth subequal or larger than penultimate basal. Palpal formula 3,2. Body of clypeus projecting to anterior edge of apron or beyond. Nuchal groove weak to strong. Posterior margin of head weakly concave to convex. Mesosoma habitus variable. Propodeal spines moderately long and angled to very long and nearly horizontal, a bisecting line usually passes well above anteroventral corner of pronotum. Propodeal spiracle not especially large or prominent; located < 1 /2 diameter to almost one diameter from edge of infradental lamella. Metapleural lobes moderately to very prominent; corner broadly to narrowly rounded. Petiolarnode more or less distinct. Petiolar keel absent to moderately well developed. Sting apparatus of specimens from four localities like that of inermis, except for less angular anteroventral corner of spiracular plate, somewhat lower valve chamber height, and in Belize and Oaxaca specimens the sting shaft is higher and slightly upturned.

Laterodorsa of head longitudinally rugose to areolate; posterior head transversely arched areolate-rugose. Pronotal sides longitudinally rugose to areolate-rugose; meso- and metapleura cornfused rugose. Dorsal face of Propodeum marked anteriorly by a distinct transverse carina, then areolate and/or transversely rugose. Head and mesosoma microsculpture obscure; intervals in macrosculpture moderately shiny. Top and sides of petiolar node effaced microareolate with very weak, indistinct macrosculpture; posterior face with weak longitudinal rugulae. Postpetiolarnode with vague microsculpture on sides; smooth dorsally.

Color brownish-yellow to brownish-yellow; dorsa of head and gaster slightly darker, appendages lighter.

Type Material

Kugler (1994) - Holotype and paratype worker, UNITED STATES: Texas, Cameron County, La Feria (W. S. Creighton) Los Angeles County Museum of Natural History [Holotype and paratype examined].


References based on Global Ant Biodiversity Informatics

  • Cancino, E.R., D.R. Kasparan, J.M.A. Coronado Blanco, S.N. Myartseva, V.A. Trjapitzin, S.G. Hernandez Aguilar and J. Garcia Jimenez. 2010. Himenópteros de la Reserva “El Cielo”, Tamaulipas, México. Dugesiana 17(1):53-71
  • Castano-Meneses, G., M. Vasquez-Bolanos, J. L. Navarrete-Heredia, G. A. Quiroz-Rocha, and I. Alcala-Martinez. 2015. Avances de Formicidae de Mexico. Universidad Nacional Autonoma de Mexico.
  • Dattilo W. et al. 2019. MEXICO ANTS: incidence and abundance along the Nearctic-Neotropical interface. Ecology
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  • Longino J. T. 2013. Ants of Honduras. Consulted on 18 Jan 2013.
  • 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.
  • O'Keefe S. T., J. L. Cook, T. Dudek, D. F. Wunneburger, M. D. Guzman, R. N. Coulson, and S. B. Vinson. 2000. The Distribution of Texas Ants. The Southwestern Entomologist 22: 1-92.
  • Olson D. M. 1991. A comparison of the efficacy of litter sifting and pitfall traps for sampling leaf litter ants (Hymenoptera, Formicidae) in a tropical wet forest, Costa Rica. Biotropica 23(2): 166-172.
  • Reynoso-Campos J. J., J. A. Rodriguez-Garza, and M. Vasquez-Bolanos. 2015. Hormigas (Hymenoptera: Formicidae) de la Isla Cozumel, Quintana Roo, Mexico (pp. 27-39). En: Castaño Meneses G., M. Vásquez-Bolaños, J. L. Navarrete-Heredia, G. A. Quiroz-Rocha e I. Alcalá-Martínez (Coords.). Avances de Formicidae de México. UNAM, Universiad de Guadalajara, Guadalajara, Jalisco.
  • Snelling R. R. 1973. Two ant genera new to the United States (Hymenoptera: Formicidae). Contributions in Science (Los Angeles) 236: 1-8.
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