| Aenictus kutai|
Jaitrong & Wiwatwitaya, 2013
So far A. kutai is known only from the type locality in a lowland fire-damaged forest.
A member of the pachycerus group. Jaitrong & Wiwatwitaya (2013) - This species is closely related to Aenictus sulawesiensis and A. sp. 84 of WJT in having smooth and shiny lateral face of pronotum. However, it is easily separated from the latter two by its head and dorsal face of pronotum being entirely sculptured (partly smooth and shiny in the latter two).
Keys including this Species
Borneo (E. Kalimantan)
Distribution based on Regional Taxon Lists
Distribution based on AntMaps
Distribution based on AntWeb specimens
Check data from AntWeb
Little is known about the biology of Aenictus kutai. The genus is comprised of species that live an army ant lifestyle. Aenictus typically prey on other ants, from other genera, or other insects such as wasps or termites. There are reports of Aenictus preying on other insects as well and even have been observed collecting honeydew from homopterans (Santschi, 1933; Gotwald, 1995) but this appears, at least from available evidence, to be uncommon. Foraging raids can occur day or night across the ground surface. Occasionally raids are arboreal. During a raid numerous workers attack a single nest or small area, with several workers coordinating their efforts to carry large prey items back to the nest or bivouac. Aenictus have a nomadic life style, alternating between a migratory phase in which nests are temporary bivouacs in sheltered places above the ground and a stationary phase where semi-permanent underground nests are formed. During the nomadic phase bivouacs move regularly, sometimes more than once a day when larvae require large amounts of food. Individual nests usually contain up to several thousand workers, although nest fragments containing only a few hundred workers are often encountered. Queens are highly specialised and look less like workers than in most ant species. They have greatly enlarged gasters (dichthadiform) and remain flightless throughout their life. New colonies are formed by the division of existing colonies (fission) rather than by individual queens starting colonies on their own.
Known only from the worker caste.
The following information is derived from Barry Bolton's New General Catalogue, a catalogue of the world's ants.
- kutai. Aenictus kutai Jaitrong & Wiwatwitaya, 2013: 99, figs. 1A, B (w.) INDONESIA.
Unless otherwise noted the text for the remainder of this section is reported from the publication that includes the original description.
Holotype: TL 4.40 mm; HL 0.98 mm; HW 0.91 mm; SL 0.85 mm; ML 1.43 mm; PL 0.35 mm, CI 94; SI 93.
Paratypes (n = 9): TL 4.20-4.40 mm; HL 0.93-0.98 mm; HW 0.85-0.91 mm; SL 0.80-0.85 mm; ML 1.35-1.43 mm; PL 0.34-0.35 mm, CI 92–94; SI 93–94.
Head in full-face view oval, slightly longer than broad, with distinctly convex sides; posterior margin convex; occipital margin bearing a collar. Antennal scape relatively short, extending beyond 2/3 of head length but not reaching posterolateral corner of head; all funicular segments each longer than broad; terminal segment slightly shorter than VII+VIII+IX. Frontal carinae well developed, fused at the level of antennal base to form a single carina, extending slightly beyond the level of posterior margin of torulus. Parafrontal ridge well developed, extending 1/3 of head length (ca. 0.45 mm). Masticatory margin of mandible with large apical tooth, followed by 15-16 denticles of two sizes, the larger alternating with 1-3 smaller; basal margin with 1-2 very small denticles just behind basal tooth. Mesosoma stout; promesonotum (seen in profile) strongly convex dorsally, sloping gradually to metanotal groove; propodeum clearly lower than promesonotum, in profile its dorsal outline almost straight; mesopleuron clearly demarcated from metapleuron by a deep groove; upper portion of mesopleuron impressed; metanotal groove present but indistinct. Propodeal junction angulate, almost right-angled; declivity of propodeum shallowly concave, and encircled with a distinct rim. Petiole sessile, almost as long as high; its dorsal outline convex, posterior face of petiole shallowly concave, and encircled with a thin rim; subpetiolar process weakly produced below; its anteroventral corner bluntly angulate. Postpetiole slightly longer than petiole, its node slightly elevated posteriorly. Femora apically swollen.
Dorsum of head longitudinally but irregularly rugose, superimposed with dense minute punctures in anterior 2/3, densely and minutely punctate in posterior 1/3; sides of head densely and minutely punctate. Mandible densely striate except in apical portion and along masticatory margin. Antennal scape densely micropunctate. Punctation on dorsum of pronotum similar to that in posterior portion of dorsum of head; lateral face of pronotum with weaker sculpture, partly shiny; remainder parts of mesosoma irregularly and coarsely sculptured, superimposed with small punctures. Petiole and postpetiole densely punctate; dorsa with irregular longitudinal rugae. First gastral tergite and sternite smooth and shiny, except for the basalmost part with dense micropunctures. Basal 2/3 of femora microreticulate, but apically 1/3 superficially reticulate and shiny.
Head and mesosoma dorsally with dense standing hairs; longest pronotal hair 0.38–0.40 mm long. Head and mesosoma reddish brown; antenna, legs, petiole, postpetiole, and gaster reddish brown or yellowish brown. Typhlatta spot absent.
Holotype worker from Indonesia, Borneo, E. Kalimantan, Kutai National Park, Teluk Kabah (0°22'N, 117°16'E), 19 Sep.1993, coll. Sk. Yamane, SKY93-09-1 (MZB). Nine paratype workers, same data as holotype (The Natural History Museum, Musee d'Histoire Naturelle Genève, SKY Collection, Natural History Museum of the National Science Museum).
The specific name is a noun in apposition referring to the traditional name of a historic region in East Kalimantan Province of Indonesia.