Workers were discovered on a bright sunny morning, running in file over a log at the edge of a native trail in open secondary rainforest in In Wamuki, New Guinea (Wilson 1964).
- 1 Identification
- 2 Distribution
- 3 Biology
- 4 Castes
- 5 Nomenclature
- 6 References
- 7 References based on Global Ant Biodiversity Informatics
Jaitrong and Yamane (2011) - A member of the currax group.A. huonicus is very similar in general appearance to Aenictus currax, Aenictus diclops, Aenictus pfeifferi, Aenictus parahuonicus, and Aenictus wayani. Among them this species is closely related to A. pfeifferi and A. parahuonicus more than the others, the former two sharing a shorter antennal scape with SI 75–94 (more than 96 in A. currax, A. diclops, and A. wayani). However A. huonicus is easily separated from A. pfeifferi by the head having some shorter standing hairs in addition to two long hairs on vertex (only 2 long standing hairs present on vertex in A. pfeifferi) and the longest pronotal hair (0.35–0.40 mm) being longer than in A. pfeifferi (0.23–0.25 mm). A. huonicus differs from A. parahuonicus in having the declivity of the propodeum encircled with a thin rim (declivity not encircled with a rim in the latter).
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 huonicus. 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 Online Catalogue of the Ants of the World.
- huonicus. Aenictus huonicus Wilson, 1964a: 465, figs. 24, 25 (w.) NEW GUINEA (Papua New Guinea).
- Type-material: holotype worker, 7 paratype workers.
- Type-locality: holotype Papua New Guinea: Huon Peninsula, Mongi-Mape Watershed, Wamuki, 800 m., 19-20.iv.1955, no.859 (E.O. Wilson); paratypes with same data.
- Type-depository: MCZC.
- Status as species: Bolton, 1995b: 59; Jaitrong & Yamane, 2011: 18 (redescription).
- Distribution: Papua New Guinea.
Unless otherwise noted the text for the remainder of this section is reported from the publication that includes the original description.
Jaitrong and Yamane (2011) - Measurements. holotype and paratypes (n = 4): TL 4.20–4.25 mm; HL 0.90–0.95 mm; HW 0.75–0.80 mm; SL 0.70–0.73 mm; ML 1.38–1.53 mm; PL 0.35–0.38 mm; CI 81–86; SI 87–94.
(holotype and paratypes). Head in full-face view clearly longer than broad, with sides slightly convex and posterior margin almost straight or feebly concave; occipital margin bearing a narrow collar. Antennal scape extending 2/3 of head length; antennal segments II–VI each longer than broad and of approximately same length; VII–IX thicker and slightly longer; X longer than VIII+IX. Frontal carina short, not extending beyond the level of posterior margin of torulus. Parafrontal ridge essentially absent. Masticatory margin of mandible with a large apical tooth followed by a medium-sized subapical tooth and 6–7 denticles. Mesosoma slender; promesonotum in profile convex dorsally and sloping gradually to metanotal groove; mesopleuron clearly demarcated from metapleuron by a groove. Propodeum in profile with convex dorsal outline; propodeal junction marked by a distinct carina; declivity of propodeum short, shallowly concave, and encircled with a thin rim; metapleural gland bulla large, raised; distance between propodeal spiracle and the bulla less than spiracular diameter; opening of the spiracle clearly circular, about 2.7 times as long as diameter of postpetiolar spiracle. Petiole slightly longer than high, with its dorsal outline convex; subpetiolar process low, with its anteroventral corner angular and ventral margin almost straight or feebly convex. Postpetiole slightly shorter than petiole and almost as long as high, with its dorsal outline convex.
Head including mandible and antennal scape entirely smooth and shiny. Pronotum smooth and shiny except for the anteriormost portion punctate; mesonotum smooth and shiny; mesopleuron sculptured, anepisternum wrinkled while katepisternum macroreticulate; mesopleuron with several irregular longitudinal ridges; matpleural gland bulla almost smooth; propodeal dorsum smooth and shiny; lateral face of propodeum with several irregular longitudinal ridges, but shiny. Petiole smooth and shiny dorsally, its anterior and posterior portion punctate, lateral face microreticulate or shagreened with smooth and shiny bottoms. Postpetiole entirely smooth and shiny. Legs entirely smooth and shiny.
Head with some shorter standing hairs in addition to two long hairs on vertex; mesosoma with relatively sparse standing hairs mixed with sparse short hairs over the surface; longest pronotal hair 0.35–0.40 mm long. Entire body dark reddish-brown, with a relatively small typhlatta spot on each occipital corner.
- Holotype, worker, Wamuki, Mongi-Mape Watershed, Huon Peninsula, 800m, Papua New Guinea, 19–20 April 1955, E.O. Wilson, Museum of Comparative Zoology.
- Paratype, 3 workers, Wamuki, Mongi-Mape Watershed, Huon Peninsula, 800m, Papua New Guinea, 19–20 April 1955, E.O. Wilson, Museum of Comparative Zoology.
Jaitrong and Yamane (2011) - Holotype and three paratype workers from New Guinea, Huon Peninsula, Mongi-Mape Watershed, Wamuki, 800 m alt., 19–20 IV 1955. E. O. Wilson leg. (Museum of Comparative Zoology, examined).
- 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. PDF
- Wilson, E. O. 1964a. The true army ants of the Indo-Australian area (Hymenoptera: Formicidae: Dorylinae). Pacific Insects. 6: 427-483 (page 465, figs. 24, 25 worker described)
References based on Global Ant Biodiversity Informatics
- Borowiec M. L. 2016. Generic revision of the ant subfamily Dorylinae (Hymenoptera, Formicidae). ZooKeys 608: 1–280.
- CSIRO Collection
- Janda M., G. D. Alpert, M. L. Borowiec, E. P. Economo, P. Klimes, E. Sarnat, and S. O. Shattuck. 2011. Cheklist of ants described and recorded from New Guinea and associated islands. Available on http://www.newguineants.org/. Accessed on 24th Feb. 2011.
- Lucky A., E. Sarnat, and L. Alonso. 2011. Ants of the Muller Range, Papua New Guinea, Chapter 10. In Richards, S. J. and Gamui, B. G. (editors). 2013. Rapid Biological Assessments of the Nakanai Mountains and the upper Strickland Basin: surveying the biodiversity of Papua New Guineas sublime karst environments. RAP Bulletin of Biological Assessment 60. Conservation International. Arlington, VA.
- Snelling R. R. 1998. Insect Part 1: The social Hymenoptera. In Mack A. L. (Ed.) A Biological Assessment of the Lakekamu Basin, Papua New Guinea, RAP 9. 189 ppages
- Snelling R. R. 2000. Ants of the Wapoga river area, Irian Jaya, Indonesia. In Mack, Andrew L. and Leeanne E. Alonso (eds.). 2000. A Biological Assessment of the Wapoga River Area of Northwestern Irian Jaya, Indonesia. RAP Bulletin of Biological Assessment 14, Conservation International, Washington, DC.
- Wilson E. O. 1964. The true army ants of the Indo-Australian area (Hymenoptera: Formicidae: Dorylinae). Pacific Insects 6: 427-483.
- Wilson E. O. 1965. A consistency test for phylogenies based on contemporaneous species. Systematic Zoology 14: 214-220.