Vicinopone conciliatrix

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Vicinopone conciliatrix
Scientific classification
Kingdom: Animalia
Phylum: Arthropoda
Class: Insecta
Order: Hymenoptera
Family: Formicidae
Subfamily: Dorylinae
Genus: Vicinopone
Species: V. conciliatrix
Binomial name
Vicinopone conciliatrix
(Brown, 1975)

Simopone conciliatrix casent0172320 profile 1.jpg

Simopone conciliatrix casent0172320 dorsal 1.jpg

Specimen labels

The lone representative of the genus Vicinopone. Bolton and Fisher (2012) - V. conciliatrix appears to be a quite widely distributed but rare species. Its rarity is more likely apparent than real because it nests and forages in trees, rarely if ever coming down to the ground. Its type-locality at Tafo, in Ghana, was within the grounds of the Cocoa Research Institute of Ghana, where a nest of the species was discovered in a thin twig of a small cocoa tree, about 2 metres above the ground, in moderate shade. The nest contained 103 workers, 2 dealate queens and a number of brood. A second, smaller nest was also found at Tafo the following year, located just a few metres from the first, but the species does not appear to have been found there again. Brown (1975) recorded two paratypes from the Democratic Republic of Congo and Yanoviak et al. (2007) retrieved conciliatrix from forest canopy in Gabon. Recently, Peter Hawkes (AFRC) has sent us excellent photographs of a hand-collected specimen found in primary forest in Tanzania (Lindi Region, Ndimba Forest Reserve, 2008 (Hawkes, Mlacha & Ninja)).


This is the only species in the genus Vicinopone.

Brown (1975) - shows a mixture of characters of Lioponera, Simopone and Cerapachys, thus tying these genera together. In general habitus (elongate head and petiole, large eyes), conciliatrix is a Simopone. The frontal carinae are fairly close together, but parallel and separate caudad; they are intermediate between the condition seen in Simopone on one hand and Lioponera-Cerapachys on the other. The lack of ocelli in the worker and the 12-merous antennae are shared by conciliatrix with the majority of (but by no means all) Cerapachys-Lioponera. Toothed tarsal claws are a character of Simopone, but one also found in a few Cerapachys, including the type species of that genus. The petiole, with its weak lateral margins and barrellike shape, combines traits of Simopone, Lioponera, and Cerapachys s.str.

Bolton and Fisher (2012) - In major details of morphology, striking contrasts between Vicinopone and all species of Simopone include the following (the state considered apomorphic is italicised).

1 Palp formula is 3,2 in Vicinopone, as opposed to 6,4 or more rarely 5,3 in Simopone.

2 Antennae have 12 antennomeres in Vicinopone, as opposed to 11 antennomeres in Simopone.

3 Scape, when laid straight back, reaches the posterior margin of the eye in Vicinopone, as opposed to the anterior margin of the eye in Simopone (SI 57–67 in Vicinopone, SI 33–56 in Simopone).

4 Ocelli are absent in Vicinopone, as opposed to present in Simopone.

5 Eyes are shifted very far forward in Vicinopone, as opposed to being near or behind the midlength in Simopone (EP 0.32–0.41 in Vicinopone, EP 0.68–1.91 in Simopone).

6 A differentiated posterior (occipital) surface to the head occurs in Vicinopone, as opposed to the lack of such a surface in Simopone.

7 Pre-occipital carina (that extends down the posterolateral margin of the head and onto the ventral surface) runs right across the ventral surface to intersect the ventral midline in Vicinopone, as opposed to the carina terminating well before it approaches the ventral midline in Simopone.

8 Metabasitarsus lacks a ventral glandular groove in Vicinopone, as opposed to the universal presence of such a groove in Simopone.

9 AII (petiole) tergite in dorsal view is elongate and barrel-shaped in Vicinopone, as opposed to flattened and laterally marginate in Simopone (AIIW/AIIL 0.68–0.75 in Vicinopone, AIIW/AIIL 0.79–1.30 in Simopone). 10 Cinctus of AIV is cross-ribbed in Vicinopone, as opposed to smooth in Simopone.


Distribution based on Regional Taxon Lists

Afrotropical Region: Democratic Republic of Congo, Gabon, Ghana (type locality), Mozambique, Uganda, United Republic of Tanzania.

Distribution based on AntMaps


Distribution based on AntWeb specimens

Check data from AntWeb



The workers are said to be size-variable, suggesting a polymorphic worker caste. Also: Bolton and Fisher (2012) - there is allometric variation in the size of the eyes, which become relatively larger with increased size. In the smallest workers measured (HW 0.32) the ratio EL/HW is 0.31. As HW increases the ratio increases, until in the largest workers (HW 0.42), EL/HW is 0.45. In full-face view the outer margins of the eyes of the smallest workers just graze the outline of the side of the head, whereas in larger workers the anterior halves of the outer margins of the eyes clearly interrupt the outlines of the sides.



The following information is derived from Barry Bolton's Online Catalogue of the Ants of the World.

  • conciliatrix. Simopone conciliatrix Brown, 1975: 79, figs. 11-13 (w.q.) GHANA.
    • Type-material: holotype worker, 105 paratype workers, 2 paratype queens.
    • Type-locality: holotype Ghana: Tafo (= New Tafo, Eastern Region, Akim District, Cocoa Research Institute of Ghana), 27.xi.1970, hollow cocoa twig, on tree (B. Bolton); paratypes: 103 workers, 2 queens with same data, 2 workers Democratic Republic of Congo (“Belg. Congo”): Yangambi, Réserve Intégrale Riv. “Luco”, 6.x.1949, C-1265 (A. Raignier & J. van Boven).
    • Type-depositories: BMNH (holotpye); BMNH, MCZC (paratypes).
    • Combination in Vicinopone: Bolton & Fisher, 2012: 74.
    • Status as species: Bolton, 1995b: 383; Bolton & Fisher, 2012: 74 (redescription).
    • Distribution: Democratic Republic of Congo, Gabon, Ghana, Tanzania.

Unless otherwise noted the text for the remainder of this section is reported from the publication that includes the original description.



Holotype worker: TL 3.2, HL 0.63, HW 0.40, scape L 0.26; greatest diameter of compound eye 0.17, WL 0.78, petiolar node L 0.35, W 0.26, postpetiole L 0.34, W 0.34 mm; CI 63, petiolar node index 74.

Paratype workers, Ghana; 6 measured, including largest and smallest of 29 from type nest series: TL 2.4-3.4, HL 0.53- 0.68, HW 0.33-0.42, scape L 0.18-0.29, greatest diameter of compound eye 0.10-0.18, petiolar node L 0.29-0.37, W 0.20-0.27, postpetiole L 0.28-0.39, W 0.27-0.35 mm; CI 60-65, petiolar node index 63-74.

Paratype workers, Yangambi, Zaire, 2 measured: falling within the limits of the Ghana series, except for slightly shorter petiolar node: L 0.33 mm in both specimens, W 0.25, 0.27 mm.; node index 78, 82.

Body slender, more or less cylindrical, including appendages, yellow in color, smooth and shining with scattered piligerous punctures, except for limited obscurely longitudinally striolate-punctate areas mesad and in front of eyes, along lower sides of trunk (especially metanotum) and lower sides of petiolar node. Space between frontal carinae very finely roughened, subopaque.

Pilosity sparse, short, fine, decumbent to suberect on head, mandibles, trunk, and legs, except for an erect hair on each humerus; more abundant and longer, decumbent to suberect hairs on nodes and gaster, especially gastric apex. Scapes and legs with a modest vestiture of short, fine, appressed to decumbent hairs; funiculi with many short, suberect to erect hairs except on apical segment, which has dense, fine micropubescence. Eyes with few extremely small hairs.

Head in full face view strongly elongate, with parallel but distinctly convex sides, subrectangular posterior angles and a finely marginate, feebly concave posterior border. Eyes large, broad-elliptical, weakly convex, situated anteriorly, only about half their length distant from mandibular insertions, with about 35-50 rather coarse facets, touching the lateral margins of the head in full-face (dorsal) view. Frontal carinae parallel, not far apart, but with a distinct space between, extending posteriorly as slightly divergent fine ridges that end near the level of the middle of the eyes, but do not extend far from the midline toward the eyes. Edges of frontal carinae raised, but not vertical, slightly broadened just behind their midlength, but not covering antennal sockets; at their anterior ends, the carinae curve laterad to form ridges around the anterior edges of the antennal sockets. Broad median lobe of clypeus with a gently convex free margin. No trace of antennal scrobes. Mandibles triangular, downcurved, with basal and masticatory margins meeting each other at an abrupt curve; masticatory margin nearly edentate, with only very low, fine crenulation or denticulation in unworn samples; stiff, fine setae on inner (ventral) side of masticatory border.

Antennae 12-merous; funiculus apically incrassate; funicular segments II through IX broader than long, I and X slightly longer than broad, apical segment more than twice as long as subapical, and very slightly wider than subapical; 4 apical segments (or 5 in some views) forming a very indistinct club, this a bit lighter in color than rest of funiculus.

Antennal scapes gradually incrassate apicad, but not as thick as in some other Simopone species; when held back, extending a little beyond the posterior border of the eye. No trace of ocelli. The fine posterior margin extends around the posterior edge of the sides of the head and meets its opposite number at the midventral groove of the head, thus encircling the true occiput. Labrum with an emarginate free border. Palpi short, segmented 3, 2.

Trunk almost 3 times as long as wide, only very feebly constricted in the middle, with fine but distinct anterior pronotal margin; faint punctate sutural lines bounding the mesonotum in front and behind. Declivity of propodeum set off from dorsum and sides by a distinct, raised semicircular margin. As seen from the side, dorsal outline of trunk nearly straight from mid-pronotum to declivity; only a very feeble impression centered on metanotal groove, and propodeal dorsum very slightly convex.

Petiole barrel- or loaf-shaped, convex in both directions, as seen from above, with convex sides and widest near the posterior third; narrowed again slightly at posterior corners, which are rounded; anterodorsal border transversely marginate; seen in side view, a fine margin commences at the anterodorsal corner and runs back obliquely along the side to or near the posterior border below mid-height; this apparently represents the "Phyracaces margin" of each side of the node. Subpetiolar process low, with a pointed anterior convexity bilaterally bearing "dimple" concavities, and a tapered posterior part. Postpetiole nearly or quite as broad as long, with convex sides and a little wider in the posterior part, but again narrowed at the posterior border, which is straight.

First gastric (IV true abdominal) segment a little broader than long (holotype: L 0.40, W 0.44 mm), widest in its posterior half, and then beginning to taper caudad; from this point, the 3 remaining visible segments tapering to apex with scarcely any intersegmental constriction. Pygidium with an impressed, nearly flat disc bordered laterally and caudad by a continuous U-shaped margin beset with 20 or more minute denticles; the stout sting issues from the true apex, which is beneath the denticulate margin.

Legs moderate in length, femora (especially fore femora) incrassate in the middle, tibiae moderately incrassate toward apices. Tarsal claws each with a small submedian tooth. Posterior tibiae each with a single broadly pectinate spur; posterior metatarsi without any obvious groove or pore on the basal flexor surface. Middle tibiae without spurs, unless one of the hairs at the apex represents a reduced spur.

Bolton and Fisher (2012) - Measurements: HL 0.53–0.68, HW 0.32–0.42, SL 0.18–0.28, EL 0.10–0.19, PW 0.22–0.32, AIIW 0.20–0.28, AIIL 0.24–0.38, AIIIW 0.26–0.37, AIIIL 0.24–0.38, WL 0.60–0.82, MFL 0.27–0.40, CI 59–63, SI 57–67, EL/HW 0.31–0.45, EP 0.32–0.41, AIIW/AIIL 0.68–0.75, AIIIW/AIIIL 0.95–1.08 (10 measured).


dealate: TL 3.6, HL 0.62, HW 0.40, scape L 0.23, greatest diameter of compound eye 0.17, WL 0.93, petiolar node L 0.37, W 0.25, postpetiole L 0.38, W 0.35 mm.; CI 65, petiolar node index 68. Ocelli well developed. Pterothorax and blackened wing stumps well developed, but the trunk still rather flat, only weakly convex above, broadest across the middle.

First gastric (IV true abdominal) segment about as long as broad, or perhaps a trifle longer than broad. Otherwise as in worker.

Paratype Specimen Labels

Type Material

Holotype worker (The Natural History Museum) taken from a nidotype series of 103 workers (The Natural History Museum, Museum of Comparative Zoology) and two dealate queens (The Natural History Museum) with larvae from a nest in a hollow twig of cacao still on the tree at Tafo (New Tafo, “Akim”), Ghana, on 27 November 1970, by Barry Bolton. The nest was about 2 meters above the ground in moderate shade. In addition, two workers from Yangambi, Reserve Integrale R. “Luco,” in what is now Zaire, 6 October 1949, A Raignier and J. van Boven, no. C-1265, are in Museum of Comparative Zoology.

Bolton and Fisher (2012) - Simopone conciliatrix Holotype worker, paratype workers and paratype queens (dealate), GHANA: Tafo, 27.xi.1970, hollow cocoa twig, on tree (B. Bolton); paratype workers, DEMOCRATIC REPUBLIC OF CONGO (“Belg. Congo” on data label): Yangambi, Réserve Intégrale Riv. “Luco”, 6.x.1949, C-1265 (A. Raignier & J. van Boven) (The Natural History Museum, Museum of Comparative Zoology) [examined].


References based on Global Ant Biodiversity Informatics

  • Bolton B., and B. L. Fisher. 2012. Taxonomy of the cerapachyine ant genera Simopone Forel, Vicinopone gen. n. and Tanipone gen. n. (Hymenoptera: Formicidae). Zootaxa 3283: 1-101.
  • 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.
  • Yanoviak S. P., B. L. Fisher, and A. Alonso. 2007. Arboreal ant diversity (Hymenoptera: Formicidae) in a central African forest. African Journal of Ecology. 46(1): 60-66.