(Smith, F., 1859)
|Based on Barden et al., 2017. Note only selected Leptomyrmex species are included.|
L. flavitarsus has been recorded in rainforest, including lowland secondary rainforest and montane rain¬forest. Nesting habits are unknown.
- 1 Identification
- 2 Distribution
- 3 Biology
- 4 Castes
- 5 Nomenclature
- 6 References
- 7 References based on Global Ant Biodiversity Informatics
This species superficially resembles the two other dark species of Leptomyrmex known to occur in New Guinea, Leptomyrmex niger and Leptomyrmex melanoticus, but can be distinguished by the abundant pubescence on the head and body, especially the pronotum, which is lacking in the others. L. flavitarsus is also relatively larger and stouter (HW 1.18–1.45 mm; WL 3.25–3.68 mm) than the other two (L. niger HW 1.01–1.25 mm; WL 3.15–3.58 mm. L. melanoticus HW 0.99–1.06 mm; WL 3.32–3.76 mm), and closely resembles the pale Leptomyrmex puberulus, but is darker in color and lacks the pubescent eyes of L. puberulus. (Lucky and Ward 2010)
Keys including this Species
Distribution based on Regional Taxon Lists
Distribution based on AntMaps
Distribution based on AntWeb specimens
Check data from AntWeb
These conspicuous ants are most often encountered individually or as small groups of 2 or 3 foragers on the surface of the ground any time of the day or night. Because of their long legs and thin bodies, they superficially resemble spiders. This is especially true when they are disturbed, as they extend their legs, raise their gasters, and run quickly to escape danger. This has led to their being given the common name "spider ants."
Nests are found in soil or in dead wood, either standing or on the ground, and are often at the base of trees. Colony sizes average a few hundred workers and a single queen. In all but a handful of species, the queen is wingless and worker-like, differing from workers only in being slightly larger and with an enlarged mesosoma. In a few species the queens are fully winged, as they are in most other ants.
When a large source of food is found, workers of Leptomyrmex will return to their nest and recruit additional workers to help utilise the newly found resource. They also use workers as "living storage vessels". These special workers, called repletes, accept liquids from returning foragers who transfer their liquid foods to these selected workers. These special workers continue to accept liquids until their gasters become greatly enlarged and extended. When enlarged, repletes cannot escape the nest and remain inside suspended from the ceiling. They can retain these fluids for extended periods and dispense it on demand when food is in short supply.
Queens of Leptomyrmex flavitarsus have not been collected.
The following information is derived from Barry Bolton's New General Catalogue, a catalogue of the world's ants.
- flavitarsus. Formica flavitarsus Smith, F. 1859a: 136 (w.) INDONESIA (Aru I.). Lucky & Ward, 2010: 34 (m.). Combination in Camponotus: Roger, 1863b: 4; in Camponotus (Tanaemyrmex): Emery, 1925b: 90; in Leptomyrmex: Shattuck, 1992c: 114.
Unless otherwise noted the text for the remainder of this section is reported from the publication that includes the original description.
Lucky and Ward (2010) – measurements (n = 10) HL 1.74–1.99, HW 1.18–1.45, MFC 0.21–0.29, IOD 0.66–0.90, SL 3.26–3.62, EL 0.28–0.43, WL 3.25–3.68, PW 0.89–1.04, DPW 0.34–0.43, HTL 3.68–4.19, HTWmin 0.12–0.14, HTWmax 0.18–0.23, CI 0.67–0.73, SI 2.47–3.03, OI 0.06–0.15, HTC 0.55–0.71.
Medium sized species (HW 1.18–1.45 mm; WL 3.25–3.68 mm) with broad head (CI 0.67–0.73), widest anterior to eyes. Sides of head convex, genae straight to slightly concave anteriorly. Behind the eyes, head gently rounding to flat postocular margin. Approximately 15 teeth and denticles interspersed along mastica¬tory margin of mandible. Anterior clypeal margin weakly concave. Eyes positioned posterior to midline of head, small and round, convex and hairless, not reaching lateral margins of head. Antennae not compressed, scapes surpassing posterior margin of head by 3/5 their length.
Dorsal face of propodeum approximately as long as declivitous face, dorsal face with a slight transverse impression on anterior end. Petiolar node thick (DPW 0.34–0.43 mm), with rounded summit; anterior face short and perpendicular to base, with shallow median longitudinal groove. Posterior face of petiole long, flat and sloping, ventral surface flat, not projecting. Gaster broadly elliptical. Legs long and slender.
Surface distinctly shagreened and shining throughout, subopaque. Pubescence long and brownish, distrib¬uted all over the body, but especially prominent on the head, pronotum and gaster. Black, bristle-like hairs on clypeus, venter and gaster. Body generally dark brown with the tarsi, femoro-tibial joints and antennal funiculus yellow.
Two worker syntypes in Oxford University Museum of Natural History. Labelled “Aru 14” and “Aru 45.” Donisthorpe (1932c: 452) records only one worker, but both specimens appear to come from the same series, and appear to have originally been mounted on a single card, that was later cut in half. Donisthorpe’s referral of this species to Camponotus is in error.
- Emery, C. 1925d. Hymenoptera. Fam. Formicidae. Subfam. Formicinae. Genera Insectorum 183: 1-302 (page 90, Combination in Camponotus (Tanaemyrmex))
- Lucky, A. 2011. Molecular phylogeny and biogeography of the spider ants, genus Leptomyrmex Mayr (Hymenoptera: Formicidae). Molecular Phylogenetics and Evolution 59: 281-292.
- Lucky, A. & Ward, P.S. 2010. Taxonomic revision of the ant genus Leptomyrmex Mayr. Zootaxa 2688: 1-67.
- Roger, J. 1863b. Verzeichniss der Formiciden-Gattungen und Arten. Berl. Entomol. Z. 7(B Beilage: 1-65 (page 4, Combination in Camponotus)
- Shattuck, S. O. 1992c. Generic revision of the ant subfamily Dolichoderinae (Hymenoptera: Formicidae). Sociobiology 21: 1-181 (page 114, Combination in Leptomyrmex)
- Smith, F. 1859a. Catalogue of hymenopterous insects collected by Mr. A. R. Wallace at the islands of Aru and Key. [part]. J. Proc. Linn. Soc. Lond. Zool. 3: 132-158 (page 136, worker described)
References based on Global Ant Biodiversity Informatics
- 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.
- Lucky A., L. E. Alonso, E. Sarnat, and J. Hulr. 2015. Ants and scolytine beetles. In: Richards, S.J. and N. Whitmore (editors) 2015. A rapid biodiversity assessment of Papua New Guinea's Hindenburg Wall region. Wildlife Conservation Society Papua New Guinea Program. Goroka, PNG.
- Lucky A., and P. S. Ward. 2010. Taxonomic revision of the ant genus Leptomyrmex Mayr (Hymenoptera: Formicidae). Zootaxa 2688: 1-67.
- Shattuck S. O. 1994. Taxonomic catalog of the ant subfamilies Aneuretinae and Dolichoderinae (Hymenoptera: Formicidae). University of California Publications in Entomology 112: i-xix, 1-241.