Rogeria micromma

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Rogeria micromma
Scientific classification
Kingdom: Animalia
Phylum: Arthropoda
Class: Insecta
Order: Hymenoptera
Family: Formicidae
Subfamily: Myrmicinae
Tribe: Solenopsidini
Genus: Rogeria
Species: R. micromma
Binomial name
Rogeria micromma
Kempf, 1961

Rogeria micromma fig 18.jpg

In Guyana it was collected in a lowland rainforest dominated by Chlorocardium (Lauraceae) trees. (LaPolla and Sosa-Calvo 2006)


Kugler (1994) - Most similar to but not quite like other species in the curvipubens species group. WL 0.45-0.52mm. Clypeal apron medially flattened. Eye tiny. Postpetiolar node subrectangular in dorsal view and not strongly vaulted in side view; anterior lip of sternum not prominent, posterior edge angular in side view. Sides of head and mesosoma and dorsal face of propodeum opaque with dense microareolate sculpture. Laterodorsa and sides of head also finely macroareolate. Propodeum free of macro sculpture. No erect hair on scapes or extensor surfaces of legs. Dorsa of head, mesosoma, nodes and gaster T1 with short, appressed hairs and longer, erect to suberect hairs. Mesosoma dorsum with 8-10 pairs of erect hair; each node with 2 pairs of posterodorsally projecting hairs.

See the nomenclature section for additional identification notes.

Keys including this Species


Guyana and Suriname

Distribution based on Regional Taxon Lists

Neotropical Region: Colombia, Ecuador, French Guiana, Guyana, Suriname (type locality).

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.


Only known from workers.


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

  • micromma. Rogeria micromma Kempf, 1961b: 509, figs. 12, 13 (w.) SURINAM. See also: Kugler, C. 1994: 69.

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

Kugler (1994) - It may be that the three micromma specimens are just unusual Rogeria curvipubens or Rogeria cuneola, but at present there are enough differences to provisionally retain this species. Eighteen curvipubens workers from other van der Drift collections in Dirkshoop and La Poulle, are very similar to micromma in size and shape, but differ as follows: 1) clypeal apron evenly convex, 2) sides of head and mesosoma shinier with effaced microsculpture, 3) sides of head with rugose macrosculpture, and 4) reduced pilosity.

Some cuneola specimens are also very similar to Rogeria micromma in shape and size, and one from Yucatán has stiff erect hairs on head, mesosoma, waist and gaster T1, but cuneola workers differ in shape of the postpetiolar sternum, as well as in clypeal shape and pilosity.

Some Rogeria alzatei from Panama, Colombia, Guyana, and French Guiana are only slightly larger (WL 0.51-0.6Bmm) than micromma and have the same pilosity and similar structure and sculpture, but they generally have distinctly larger eyes with more than 10 facets, have a higher, more compact mesosoma (MHI 1.00-1.04), and generally narrower propodeal spines. Several alzatei from northern Colombia have reduced eyes (7-8 facets) and one has wider propodeal spines, but those Colombian ants are larger, have a higher mesosoma, and more abundant erect pilosity. See also Rogeria minima’’.



Kugler 1994 fig 71-78

Kugler (1994) - TL 1.7-1.8, HL 0.44-0.51, HW 0.37-0.45, SL 0.28-0.35, EL 0.02-0.04 (2-5 facets), PW 0.28-0.30, WL 0.45-0.52, SpL 0.07-0.08, PetL 0.17-0.18, PetW 0.10-0.13, PpetL 0.10-0.11, PpetW 0.13-0.15mm, CI 0.84-0.88, OI 0.05-0.08, SI 0.76-0.79, PSI 0.15-0.16, MHI 0.92-0.96. N=3

The following supplements diagnosis and Kempf (1961). Mandibles 5-toothed to 6-toothed; basal tooth not larger than penultimate basal. Mesosoma profile of holotype interrupted by a weak metanotal groove followed by two transverse carinulae, but profiles of La Poulle and Brazil specimens uninterrupted. Brazil specimen with narrower propodeal spines than in types, and propodeal spiracle closer to posterior edge of propodeum. Petiole short (PetL/WL 0.35-0.38), with ventral keel and tooth.

In Surinam specimens, vague microareolate microsculpture densely covers head, dorsum of mesosoma, dorsal face of propodeum, petiole and postpetiole of types, producing a weakly shining, granular appearance. Brazil specimen similar, except for smoother ventral petiolar peduncle and postpetiolar dorsum. Sides of mesosoma and posterior surface of head more distinctly microareolate. Anterior of pronotal disc with 1 to 2 transverse rugae followed by longitudinally rugose to areolate-rugose macrosculpture that disappears into microsculpture on meso- and metanota. Sides of mesosoma with sparse, faint longitudinal rugulae on meso- and metapleura. Nodes microareolate; more effaced on postpetiole.

Erect hairs of Dirkshoop specimen all trichoid; but thicker and stiff on the La Poulle specimen, at least some cuneate; erect hairs on the Belem specimen seem intermediate.

Color brownish-yellow; legs, mandibles and antennae sometimes slightly lighter. Frontoclypeal region not lighter than rest of head.

Type Material

Kugler (1994) - Holotype worker, SURINAM: Dirkshoop (J. van der Drift) Museu de Zoologia da Universidade de Sao Paulo [Holotype and La Poulle paratype examined].


References based on Global Ant Biodiversity Informatics

  • Delabie J. H. C., S. Lacau, I. C. do Nascimento, A. B. Casimiro, and I. M. Cazorla. 1997. Communaute des fourmis de souches d'arbres morts dans trois reserves de la foret atlantique bresilienne (Hymenoptera, Formicidae). Ecologia Austral7: 95-103.
  • 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. 1961. A survey of the ants of the soil fauna in Surinam (Hymenoptera: Formicidae). Studia Entomologica 4: 481-524.
  • Kempf W. W. 1962. Miscellaneous studies on neotropical ants. II. (Hymenoptera, Formicidae). Studia Entomologica 5: 1-38.
  • Kempf, W.W. 1972. Catalago abreviado das formigas da regiao Neotropical (Hym. Formicidae) Studia Entomologica 15(1-4).
  • Kugler C. 1994. A revision of the ant genus Rogeria with description of the sting apparatus (Hymenoptera: Formicidae). Journal of Hymenoptera Research 3: 17-89.
  • Lapolla J. S., and J. Sosa-Calvo. 2006. Review of the ant genus Rogeria (Hymenoptera: Formicidae) in Guyana. Zootaxa 1330: 59-68.
  • Lapolla, J. S., and B. L. Fisher. "Review of the ant genus Rogeria (Hymenoptera: Formicidae) in Guyana." Zootaxa 1330 (2006): 59-68.
  • Lapolla, J.S., T. Suman, J. Soso-Calvo and T.R. Schultz. 2006. Leaf litter ant diversity in Guyana. Biodiversity and Conservation 16:491–510
  • Mirmecofauna de la reserva ecologica de San Felipe Bacalar
  • Schmidt F. A., and R. R. C. Solar. Is it important to collect hypogaeic ants? How to collect them? Biológico, São Paulo 69(2): 267-270.
  • Siqueira de Castro F., A. B. Gontijo, P. de Tarso Amorim Castro, and S. Pontes Ribeiro. 2012. Annual and Seasonal Changes in the Structure of Litter-Dwelling Ant Assemblages (Hymenoptera: Formicidae) in Atlantic Semideciduous Forests. Psyche doi:10.1155/2012/959715
  • 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