Nothing is known about the biology of Strumigenys nannosobek.
Bharti & Akbar (2013) - A member of the Strumigenys murphyi-group. This is the only species of the group (murphyi group) to have long erect hairs on the middle and hind tibiae and basitarsi, and is the only species to have hairs on the leading edge of the scape that are universally curved toward the apex of the scape. It also has the longest mandibles yet recorded in the group (Bolton, 2000).
Bolton (2000) - This is the only species of the group to have long erect hairs on the middle and hind tibiae and basitarsi, and is the only species to have hairs on the leading edge of the scape that are universally curved toward the apex of the scape. It also has the longest mandibles yet recorded in the group.
Keys including this Species
Distribution based on Regional Taxon Lists
Distribution based on AntMaps
Distribution based on AntWeb specimens
Check data from AntWeb
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.
The following information is derived from Barry Bolton's New General Catalogue, a catalogue of the world's ants.
- nannosobek. Pyramica nannosobek Bolton, 2000: 453 (w.) BHUTAN. Combination in Strumigenys: Baroni Urbani & De Andrade, 2007: 124
Unless otherwise noted the text for the remainder of this section is reported from the publication that includes the original description.
Holotype. TL 1.5, HL 0.35, HW 0.42, CI 120, ML 0.18, MI 51, SL 0.20, SI 48, PW 0.25, AL 0.42. Inner margin of mandible with a series of medially directed small hairs and with 6-7 small preapical teeth, the third from the base is the largest, narrowly triangular and located at about the midlength of the mandible (this tooth is doubled in one of the paratypes). Apicodorsal tooth the longest and overlaps its counterpart from the opposing mandible, spiniform but not extending beyond the outer margin of the opposing mandible at full closure. Anterior clypeal margin with a few short, flattened projecting hairs; clypeal dorsum only with small orbicular hairs. Dorsum of head posterior to clypeus without orbicular hairs. Transverse crest of vertex conspicuous, approximately straight across most of vertex but on each side curved forward toward the anterolateral angle of the occipital lobe. Sides of occipital lobes in full-face view more or less straight, weakly convergent posteriorly. Leading edge of scape with a row of narrowly spatulate hairs that are curved toward the apex of the scape. Apex of subbasal lobe of scape with an elongate spatulate hair that is directed anteriorly; inner margin of subbasal lobe with 2-3 narrowly spoon-shaped hairs that curve toward the apex of the lobe. Head and alitrunk otherwise with minute inconspicuous ground-pilosity but without standing hairs of any form. Eye minute, of 2-3 very small ommatidia. Head finely and densely reticulate-punctate. Pronotal dorsum with a few feeble, posteriorly divergent fine longitudinal costulae; dorsum depressed along line of promesonotal junction. Mesonotum in profile very shallowly convex, highest posteriorly. Pleurae smooth. Dorsal (outer) surfaces of middle and hind tibiae, and middle and hind basitarsi, each with 1-2 long erect freely projecting hairs (obscured by glue in holotype, visible in paratypes). Petiole and postpetiole without standing hairs but first gastral tergite with short erect simple pilosity. Petiole node broader than long in dorsal view, finely shagreenate and dull. Disc of postpetiole finely shagreenate to smooth, much less strongly sculptured than petiole node. Basigastral costulae strongly developed, longer than disc of postpetiole.
Paratypes. TL 1.4-1.5, HL 0.33-0.35, HW 0.39-0.42, CI 118-120, ML 0.18-0.19, MI 51-55, SL 0.19-0.20, PW 0.23-0.25, AL 0.40-0.43 (4 measured).
Holotype worker, Bhutan: Kamjee, 24.4., Nat.-Hist. Museum Basel - Bhutan Expedition 1972 (no collector's name) (Naturhistorisches Museum, Basel).
Paratypes. 1 worker with same data as holotype; 3 workers, Bhutan: Phuntsholing, 2/400 m., 15.4., Nat.-Hist. Museum Basel - Bhutan Expedition 1972 (no collector' s name) (NHMB, The Natural History Museum).
- Baroni Urbani, C. and 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.
- Bharti, H. & Akbar, S.A. 2013. Taxonomic studies on the ant genus Strumigenys Smith, 1860 (Hymenoptera, Formicidae) with report of two new species and five new records including a tramp species from India. Sociobiology 60, 387-396 (DOI: 10.13102/sociobiology.v60i4.387-396).
- Bolton, B. 2000. The ant tribe Dacetini. Memoirs of the American Entomological Institute. 65:1-1028. (page 453, worker described)