The types were from "a series of 21 workers taken running in broken file over logs in wet forest....Some of the ants were carrying white pharate adults of a small Pheidole species, and they disappeared into cracks in a large rotten log."
- 1 Identification
- 2 Distribution
- 3 Biology
- 4 Castes
- 5 Nomenclature
- 6 References
- 7 References based on Global Ant Biodiversity Informatics
Brown (1975) - This species occupies a taxonomic position of special importance, because it links the old Cerapachys s.str. with Phyracaces (by antennal form and shape of petiole) on the one hand, and with Simopone (by separate, merely obliquely raised frontal lobes, demiscrobes, and very large eyes) on the other. The concave, medially striate disc of the petiolar node will serve to distinguish L. livida from all congeners.
Distribution based on Regional Taxon Lists
Distribution based on AntMaps
Distribution based on AntWeb specimens
Check data from AntWeb
Brown (1975) - I can add observations on Lioponera mayri and Lividopone livida in the rain forest of Madagascar, and on Parasyscia indica in the Western Ghats of southern India. All 3 species were found attacking, or returning from attacks on, nests of Pheidole species, and the booty being transported consisted of larvae, pupae, pharate adults, and even in some cases dead but fully pigmented Pheidole soldiers and workers. These raids were all observed in progress near midday in shaded situations, and the raiding workers returned one by one over logs and roots along an obvious odor trail with their prey.
The following information is derived from Barry Bolton's Online Catalogue of the Ants of the World.
- livida. Cerapachys lividus Brown, 1975: 64, figs. 46, 47, 50 (w.) MADAGASCAR.
- Type-material: holotype worker, 20 paratype workers.
- Type-locality: Madagascar: nr Périnet, 18.iii.1969, “on rail line from Tananarive to Tamatave”, rainforest, rotten wood (W.L. Brown); paratypes with same data.
- Type-depositories: MCZC (holotype); BMNH, MCZC (paratypes).
- Combination in Lividopone: Fisher & Bolton, 2016: 304; Borowiec, M.L. 2016: 165.
- Status as species: Bolton, 1995b: 143; Fisher & Bolton, 2016: 304.
- Distribution: Madagascar.
Unless otherwise noted the text for the remainder of this section is reported from the publication that includes the original description.
Holotype: TL 5.3, HL 1.00, HW 0.97 (CI 97), ML 0.19, WL 1.44, petiolar node L 0.51, petiolar node W 0.74, antennal scape L 0.56, greatest diameter of eye 0.30 mm (largest worker of type series).
Paratypes: Measurements are of smallest paratype: TL 4.8, HL 0.94, HW 0.87 (CI 93), ML 0.15, WL 1.30, petiolar node L 0.48, petiolar node W 0.69, antennal scape L 0.51, greatest diameter of eye 0.28 mm.
Compound description. In larger specimens, head very nearly as broad as long; ignoring anterior projections over the mandibles, width is equal to or very slightly greater than length. In small specimens, head slightly narrower in relation to length. This is a thickset species with large, posteriorly placed eyes. A few of the larger specimens also have a weakly developed median ocellus, or ocellar pit, and in at least 2 specimens, minute, paired, posterior ocelli or pits are present.
Characters to be especially noted are the lack of a median tooth or tubercle on the clypeus; the obliquely raised, separated, frontal lobes and carinae; the large, smooth, impressed area mesad of each eye, serving as a demiscrobe for the unusually large, thick 12-merous antennae; and, bordering each impressed area laterad, the distinct anteocular groove connecting the circumocular (orbital) groove with the lateral carina of the cheek. The scapes reach to about the middle of the eyes; apical segment of antenna about 3 X as long as penultimate segment, and slightly thicker. Palpi segmented 3,2, the two segments of the labial palpi both long.
Trunk boxlike, with sutureless dorsum gently convex in both directions; pleura vertical, curving sharply into dorsum above. Pronotum sharply marginate anteriorly, with a groove inside the margin; this groove, becoming wider and deeper ventrad, crosses the lower part of each side of the pronotum and continues horizontally across the middle of the side of the mesothorax as a deep mesopleural suture, then curves downward to form the suture between meso- and metapleuron. There is also a horizontal sulcus each, both above and below the meatus of the metapleural gland. Propodeal declivity concave, bounded above and on the sides by a narrow, raised margin or carina. Propodeal spiracle situated down low, small, and nearly circular.
Petiole: note the concave dorsal surface and marginate anterodorsal edge, the latter very slightly convex in the middle, but otherwise straight. Sides of petiole steep, but not separated from dorsum by a margin. The longitudinal striation of the disc is distinctive. Sting stout. Pygidium with a smooth, shining, impressed disc, its laterapical margins raised, bearing a row of sharp denticles.
Body surface smooth, with widely spaced, moderately coarse punctures, mostly piligerous, sparse on sides of trunk. Concave areas inside eyes and anterior clypeus impunctate; cheeks mesad of carinae, tibiae and tarsi, and sides of pygidium densely, finely, indistinctly punctulate, subopaque. Pilosity of fine, slightly curved hairs of moderate length, mostly decumbent to subdecumbent, fairly abundant, longest on gaster; shorter and dense on legs and antennae. Longer hairs more nearly erect in some speciments. Body black, with a rich, opalescent blue sheen; antennal funiculi, legs, and apex of gaster brown.
Apical tibial spurs narrowly pectinate, the posterior pair slightly larger than those of middle legs; tarsal claws slender and simple.
Holotype (Museum of Comparative Zoology) and paratype (MCZ, The Natural History Museum, and elsewhere) from a series of 21 workers taken running in broken file over logs in wet forest near Perinet, on the rail line from Tananarive to Tamatave in Madagascar (Brown leg.). Some of the ants were carrying white pharate adults of a small Pheidole species, and they disappeared into cracks in a large rotten log that could not be opened with the tools available.
- Brown, W. L., Jr. 1975. Contributions toward a reclassification of the Formicidae. V. Ponerinae, tribes Platythyreini, Cerapachyini, Cylindromyrmecini, Acanthostichini, and Aenictogitini. Search Agric. (Ithaca N. Y.) 5(1 1: 1-115 (page 64, figs. 46, 47, 50; worker described)
- Fisher, B. L. 1997a. Biogeography and ecology of the ant fauna of Madagascar (Hymenoptera: Formicidae). J. Nat. Hist. 31: 269-302 (page 285, see also)
References based on Global Ant Biodiversity Informatics
- Brown W. L., Jr. 1975. Contributions toward a reclassification of the Formicidae. V. Ponerinae, tribes Platythyreini, Cerapachyini, Cylindromyrmecini, Acanthostichini, and Aenictogitini. Search Agric. (Ithaca N. Y.) 5(1): 1-115.
- Fisher B. L. 1997. Biogeography and ecology of the ant fauna of Madagascar (Hymenoptera: Formicidae). Journal of Natural History 31: 269-302.
- Fisher B. L. 2003. Formicidae, ants. Pp. 811-819 in: Goodman, S. M.; Benstead, J. P. (eds.) 2003. The natural history of Madagascar. Chicago: University of Chicago Press, xxi + 1709 pp.