Known from two collections, one of which states it was gathered "from vegetation."
- 1 Identification
- 2 Distribution
- 3 Biology
- 4 Castes
- 5 Nomenclature
- 6 References
- 7 References based on Global Ant Biodiversity Informatics
Bolton (2000) - A member of the Strumigenys schulzi-group. Within the group the combination of convex clypeal margin and distribution and form of pilosity, together with the possession of mostly smooth unsculptured pleurae and side of propodeum, is diagnostic of grytava.
Keys including this Species
Latitudinal Distribution Pattern
Latitudinal Range: 11.267° to -2.9667°.
- 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.
The following information is derived from Barry Bolton's Online Catalogue of the Ants of the World.
- grytava. Pyramica grytava Bolton, 2000: 220 (w.) COLOMBIA. Combination in Strumigenys: Baroni Urbani & De Andrade, 2007: 120
Unless otherwise noted the text for the remainder of this section is reported from the publication that includes the original description.
Bolton (2000) - Holotype. TL 1.6, HL 0.45, HW 0.33, CI 73, ML 0.08, MI 18, SL 0.20, SI 61, PW 0.21, AL 0.43. Anterior c1ypeal margin evenly convex. Eye relatively large for such a small species, with 4-5 ommatidia in the longest row and about 12 ommatidia in total. Dentition with teeth 1-5 from the base all narrowly triangular and acute, tooth 3 appearing slightly the longest. With mandibles fully closed the masticatory margin proximal of the basal most tooth, a distance about equal to the length occupied on the margin by teeth 1-3 inclusive, is filled with a low, flat basal lamella. Scape slightly dorsoventrally compressed and relatively slender; broadest point of scape is proximal of its midlength. With head in full-face view an anteriorly curved spatulate hair projects laterally in apicoscrobal position, but this hair is not radically different in shape or size from others that precede it on the upper scrobe margin, merely somewhat more elevated. In profile dorsum of head between highest point of vertex and occipital margin with 1-2 pairs of anteriorly curved short hairs that are only slightly longer and more erect than the spatulate ground-pilosity. Pronotal humeral hair short and stout, weakly remiform. Mesonotal dorsum with a single pair of similar standing hairs and similar hairs also present on waist segments and first gastral tergite. Entire katepisternum and most of metapleuron and side of propodeum smooth and shining. Petiole and postpetiole finely reticulate-punctate to reticulate-shagreenate dorsally, the former broader than long in dorsal view. Ventral surface of petiole with a lamellate process anteriorly, followed by an extremely slender crest that is only a tiny fraction of the depth of the peduncle. Basigastral costulae sharply defined and extending over the basal one-fifth to one-quarter of the tergite.
Paratype. TL 1.6, HL 0.45, HW 0.32, CI 71, ML 0.07, MI 16, SL 0.19, SI 59, PW 0.21, AL 0.41.
Bolton (2000) - Holotype worker, Colombia: Magdalena, Bahia de Neguange, P. N . Tayrona, 25 km. NE Santa Marta, 11°21'N, 74°05'W, 30.ix.1985, low vegetation (H. G. Maller) (The Natural History Museum). Paratype. 1 worker with same data as holotype (University of California, Davis).
- 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).
- Baroni Urbani, C. & De Andrade, M.L. 2007. The ant tribe Dacetini: limits and constituent genera, with descriptions of new species. Annali del Museo Civico di Storia Naturale “G. Doria” 99:1-191.
- Bolton, B. 2000. The ant tribe Dacetini. Memoirs of the American Entomological Institute. 65:1-1028. (page 220, worker described)
References based on Global Ant Biodiversity Informatics
- Achury R., and A.V. Suarez. 2017. Richness and composition of ground-dwelling ants in tropical rainforest and surrounding landscapes in the Colombian Inter-Andean valley. Neotropical Entomology https://doi.org/10.1007/s13744-017-0565-4
- Bolton, B. 2000. The Ant Tribe Dacetini. Memoirs of the American Entomological Institute 65
- Navarro, E.V. Vergara, H. Echavarria Sanchez, F.J. Serna Cardona. 2007. Hormigas (Hymenoptera: Formicidae) asociadas al arboretum de la Universidad Nacional de Colombia, sede Medellin. Boletín Sociedad Entomológica Aragonesa 40:497-505.
- 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.
- 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