Wheeler, W.M. & Chapman, 1930
Nothing is known about the biology of this species.
- 1 Identification
- 2 Distribution
- 3 Biology
- 4 Castes
- 5 Nomenclature
- 6 References
- 7 References based on Global Ant Biodiversity Informatics
A member of the laeviceps species group. Jaitrong and Yamane (2011) - A. alticola is most similar to Aenictus luzoni in having the subpetiolar process low and anteriorly angulate; the ventral appendage not spiniform. However, this species is distinctly larger than the latter (HW 0.80–0.85 in A. alticola; 0.78 in A. luzoni). The ventral appendage of the subpetiolar process is high and subtriangular in A. alticola, but rudimentary, with the highest point at anterior portion in A. luzoni. Antennal scape is almost as long as or longer than head width in A. alticola (SI 100–106), while it is shorter than head width in A. luzoni (SI 97).
Keys including this Species
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 alticola. 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.
Only known from the worker caste.
The following information is derived from Barry Bolton's Online Catalogue of the Ants of the World.
- alticola. Aenictus (Typhlatta) alticola Wheeler, W.M. & Chapman, in Wheeler, W.M. 1930g: 205, fig. 5a-d (w.) PHILIPPINES (Luzon I.).
- Type-material: lectotype worker (by designation of Jaitrong & Yamane, 2011: 25), 20 paralectotype workers.
- Type-locality: lectotype Philippines: Luzon, Bontoc, Polis Pass, 6000 ft (J.W. Chapman); paralectotypes with same data.
- Type-depository: MCZC.
- Status as species: Chapman & Capco, 1951: 12; Chapman, 1963: 263; Wilson, 1964a: 445; Baltazar, 1966: 231; Bolton, 1995b: 58; Jaitrong & Yamane, 2011: 25 (redescription).
- Distribution: Philippines (Luzon).
Jaitrong and Yamane (2011) - Measurements. Worker lectotype and paralectotypes (n = 6): TL 4.35–4.75 mm; HL 0.90–1.00 mm; HW 0.80–0.85 mm; SL 0.78–0.88 mm; ML 1.43–1.50 mm; PL 0.30–0.35 mm; CI 84–87; SI 100–106.
Redescription (lectotype and paralectotypes). Head in full-face view clearly longer than broad, with sides slightly convex and posterior margin convex; occipital margin bearing a narrow collar. Antennal scape extending beyond midlength of head, but not reaching the posterolateral corner of head; antennal segments II–X each longer than broad; II slightly longer than each of III–VI; VII, VIII and IX combined almost as long as terminal segment (X). Frontal carina short, not reaching the level of the posterior margin of torulus. Parafrontal ridge short and ill defined, or absent. Anterior margin of clypeus convex and bearing 6–7 denticles. Masticatory margin of mandible with a large apical tooth followed by a medium-sized subapical tooth, 5–6 denticles, and a medium-sized basal tooth; basal margin sinuate with a series of 2–3 ill-defined denticles. Mesosoma rather elongate and stout; promesonotum in profile strongly convex dorsally and sloping to metanotal groove; metanotal groove very weak. Propodeal junction evenly rounded; declivity not margined dorsally and laterally. Petiole subsessile and short, its node almost as long as high and rounded dorsally; subpetiolar process well developed, triangular, its apex directed downward. Postpetiole shorter than petiole, with globular node.
Head entirely smooth and shiny. Mandible very finely striate except along masticatory and outer margins. Antennal scape almost smooth and shiny. Mososoma extensively smooth and shiny; upper portion of mesopleuron and metapleuron provided with about 10 longitudinal, irregular rugulae; dorsa of mesonotum and propodeum superficially sculptured; metanotal groove bearing short longitudinal rugulae; propodeal dorsum with several short longitudinal rugae in front of the junction. Petiole and postpetiole entirely smooth and shiny. Legs entirely smooth and shiny.
Head and mesosoma with relatively sparse standing hairs mixed with sparse short hairs over the surface; longest pronotal hair 0.20–0.25 mm long. Entire body reddish-brown except for vertex of head darker than other parts of body; ventral surface of antennal segments VII–X pale yellow. Typhlatta spot located anterior to occipital corner.
Described from numerous workers taken by Dr. Chapman from a single large colony found raiding in Polis Pass, Bontoc, Luzon, at an altitude of 6,000 feet.
Jaitrong and Yamane (2011) - Twenty-one syntype workers on three pins (two on a pin, eight on another, eleven on the other) from Philippines, Luzon, Bontoc, Polis Pass, 1,800 m (Museum of Comparative Zoology, examined). One worker among them (top on the first pin) is selected as the lectotype, the others as paralectotypes. Collected by J.Chapman
- Chapman, J. W.; Capco, S. R. 1951. Check list of the ants (Hymenoptera: Formicidae) of Asia. Monogr. Inst. Sci. Technol. Manila 1: 1-327 (page 12, checklist)
- Jaitrong, W. & Yamane, S. 2011. Synopsis of Aenictus species groups and revision of the A. currax and A. laeviceps groups in the eastern Oriental, Indo-Australian, and Australasian regions (Hymenoptera: Formicidae: Aenictinae). Zootaxa, 3128, 1–46.
-  Wheeler, W. M. 1930j. Philippine ants of the genus Aenictus with descriptions of the females of two species. J. N. Y. Entomol. Soc. 38: 193-212 (page 205, fig. 5 worker described)
-  Wilson, E. O. 1964a. The true army ants of the Indo-Australian area (Hymenoptera: Formicidae: Dorylinae). Pac. Insects 6: 427-483 (page 445, see also)
References based on Global Ant Biodiversity Informatics
- Borowiec M. L. 2016. Generic revision of the ant subfamily Dorylinae (Hymenoptera, Formicidae). ZooKeys 608: 1–280.
- Chapman J. W. 1965. Studies on the ecology of the army ants of the Philippines genus Aenictus Schuckard (Hymenoptera: Formicidae). Philippine Journal of Science. 93: 551-595.
- Chapman, J.W. and S.R. Capco. 1951. Check list of the ants (Hymenoptera: Formicidae) of Asia. Monographs of the Institute of Science and Technology (Manila) 1: 1- 327