Eurhopalothrix isabellae

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Eurhopalothrix isabellae
Scientific classification
Kingdom: Animalia
Phylum: Arthropoda
Class: Insecta
Order: Hymenoptera
Family: Formicidae
Subfamily: Myrmicinae
Tribe: Attini
Genus: Eurhopalothrix
Species: E. isabellae
Binomial name
Eurhopalothrix isabellae
(Mann, 1919)

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Specimen Labels

The holotype worker was collected from beneath a log in forest habitat.

Identification

The mandibular form and dentition immediately distinguish this peculiar species. The mesosomal sculpturation is heavier than that of any known Eurhopalothrix procera variant, and the vestiture is less strongly developed. (Taylor 1968)

Keys including this Species

Distribution

Latitudinal Distribution Pattern

Latitudinal Range: -8° to -8°.

 
North
Temperate
North
Subtropical
Tropical South
Subtropical
South
Temperate

Distribution based on Regional Taxon Lists

Indo-Australian Region: Solomon Islands (type locality).

Distribution based on AntMaps

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Distribution based on AntWeb specimens

Check data from AntWeb

Countries Occupied

Number of countries occupied by this species based on AntWiki Regional Taxon Lists. In general, fewer countries occupied indicates a narrower range, while more countries indicates a more widespread species.
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Estimated Abundance

Relative abundance based on number of AntMaps records per species (this species within the purple bar). Fewer records (to the left) indicates a less abundant/encountered species while more records (to the right) indicates more abundant/encountered species.
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Biology

Explore-icon.png Explore Overview of Eurhopalothrix biology 
Little is known about the biology of most species in this genus. Nests are rarely found, and queens and males have not been collected for many species. Longino (2013) summarized their biology "Eurhopalothrix specimens are encountered almost exclusively in samples from mass extraction techniques that recover small arthropods in sifted litter, rotten wood, and soil. Densities, at least in the northern Neotropics, are usually low, with workers occurring in < 10% of quantitative samples of 1 m2 litter plots, but occasionally may reach densities as high as 40% of samples. Live colonies of Old World Eurhopalothrix were observed by Wilson (1956) and Wilson and Brown (1984), and a Costa Rican colony of Basiceros manni was observed by Wilson and Hölldobler (1986). All basicerotines, including Eurhopalothrix, are thought to be predators in tropical leaf litter, relying on stealth or sit-and-wait techniques. Sampled specimens are often coated with a thin layer of clay, especially on the face, which is thought to function as camouflage, enhancing crypsis (Hölldobler & Wilson, 1986). Highly specialized spatulate setae may be instrumental in acquisition and adherence of the clay layer (Hölldobler & Wilson, 1986)."

Castes

Nomenclature

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

  • isabellae. Rhopalothrix isabellae Mann, 1919: 357, fig. 35 (w.) SOLOMON IS. Combination in Eurhopalothrix: Brown & Kempf, 1960: 225. See also: Taylor, 1968b: 344.

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

Description

Worker

Worker. Length 3 mm.

Head about as long as broad; strongly excavated behind and with obtusely angulate corners ; oblique portions of sides with straight margin. Clypeus narrowed behind and broadly and shallowly concave in front; the suture separating it from the front shallow and rather poorly defined. Mandibles strongly constricted at basal third and much more slender than in the related species. Antennal scapes at base about a third as broad as long; funicular joints two and three only slightly transverse, joints three and four longer than broad, terminal joint longer than the four preceding joints together. Pronotum shallowly impressed at middle and obtusely gibbous on either side; humeral angles rounded, without any indi:!ation of tubercles. Promesonotal suture obsolete. Mesonotum slightly convex in front, and depressed behind. Mesoepinotal suture distinct. Base of epinotum strongly impressed mesally, marginate at sides of impression, separated from the concave declivous portion by an acute margin; spines short and obtuse apically, their bases extended as narrow lamellae along borders of declivity. Petiolar node longer than broad, slightly broadest apically and very feebly convex at sides and front; flat above; about as long as peduncle. Postpetiole one and a third times broader than long, narrowed in front, sides little convex; dorsal surface with a faint medial impression which terminates in front in a broad and shallow fovea; strongly impressed at apex and elevated into an obtuse tubercle on either side of impression. First gastric segment indistinctly impressed at middle of base.

Mandibles shining and punctate. Head feebly shining. Clypeus strongly and foveolately punctate; front reticulately and rugosely punctate; vertex with two large shallow foveae and cribriform punctures between. Promesothorax coarsely and reticulately costate and subopaque. Epinotum at sides more finely costate; impressed portion foveolately punctate; declivity smooth and shining. Petiole finely rugose. Postpetiole and gaster more shining and uniformly cribrate. Antennae and legs coarsely and densely subopaque.

Fine, squamiform hairs on head and antennal scapes, coarse ones on legs. Clavate hairs on legs, outer border of scape and one in each of the two foveae on vertex; fine hairs on funiculus, tarsi, and ventral surface of gaster.

Fuscopiceous; legs, mandibles, antennae, and lamellate borders of epinotum fuscorufous. Hair white.


Taylor (1968) - Holotype worker. Dimensions: HL, 0.85; HW, 0.89; CI, 105; SL, 0.55; SI, 62; greatest diameter of eye, 0.06; PW, 0.52; WL, 1.07; petiolar node width, 0.26. The following notes supplement Mann's original description:

(1) Basal mandibular tooth a broad, low, blade-like structure, about twice as wide at base as the acutely triangular succeeding teeth.

(2) Dorsum of petiolar node distinctly longer than broad, its midline length almost 1.2 times the maximum width.

(3) Head feebly shining, with somewhat effaced medium punctate-rugosity. Mes- and metepisternites, posterolateral parts of propodeum, and lateral areas of petiolar peduncle shining, moderately finely punctate. Propodeal declivity smooth and shining, divided transversely by a fine carina. Gastric sclerites moderately shining, almost entirely cribrately punctate (punctural diameters and interpunctural distances averaging about 0.01 mm).

Additional worker material. These specimens have the following dimensions: TL, c. 2.9-3.5; HL, 0.69-0.82; HW, 0.72-0.86; CI, 104-105; ML, 0.20-0.23; MI, 28-29; SL, 0.41-0.50; SI, 57-60; greatest diameter of eye 0.06-0.08; PW, 0.42-0.49; WL, 0.78-0.95; petiolar node width, 0.20-0.22; postpetiole width, 0.45-0.51; gastric width, 0•29-0' 34. They differ from the holotype as follows:

(1) Smaller size.

(2) Mandibles less narrowed anteriorly and thus more distinctly triangular, with outer borders less concave and posterior borders slightly less oblique, so that the triangular gap between the closed jaws and the clypeus is less extensive.

(3) Occipital border slightly less deeply emarginate in frontal view.

(4) Metanotal groove less distinctly impressed on mesosomal dorsum.

(5) Petiolar dorsum at most only minutely longer than broad.

(6) Median longitudinal depression of postpetiole less pronounced.

(7) Head less distinctly sculptured, obscure and finely punctate-rugose, the overall effect perhaps best described as coarsely shagreened. Mes- and metepisternites, posterolateral parts of propodeum, and sides of petiolar peduncle smooth, but less strongly shining than in holotype, due to an overall minutely granular micro-sculpture, which has a slight metallic lustre in some lights. Propodeal declivity divided into upper and lower portions by a sharp transverse carina; lower portion impunctate, smooth and shining; upper portion sub opaque, with scattered fine punctures and with 4 or 5 vague transverse rugae, best seen in crosslight. First gastric tergite moderately shining, with vestigial traces of effaced coarse puncturation, most distinct at edges. Sternite coarsely punctate, as in holotype.

(8) Cephalic ground pilosity as in Eurhopalothrix greensladei, essentially lacking on frons except for outer edges of occipital lobes. Dorsa of petiole and postpetiole with distinct, scattered, whitish hairs, about 0.02 mm long. (The hairs in these positions are much less distinct on the holotype, which has them distinctly developed on the frons, unlike the Vella Lavella specimens). Enlarged erect hairs restricted to a single verticoccipital pair, and those at gastric apex, as in the holotype.

(9) Colour as in E. greensladei, somewhat darker than the holotype is currently; judging from Mann's description the latter has probably faded.

Type Material

Ysabel: Fulakora. The single worker of this anomalous species was found beneath a log in the forest.

References

  • Brown, W. L., Jr.; Kempf, W. W. 1960. A world revision of the ant tribe Basicerotini. Stud. Entomol. (n.s.) 3: 161-250 (page 225, Combination in Eurhopalothrix)
  • Mann, W. M. 1919. The ants of the British Solomon Islands. Bulletin of the Museum of Comparative Zoology 63: 273-391 (page 357, fig. 35 worker described)
  • Taylor, R. W. 1968c. Notes on the Indo-Australian basicerotine ants (Hymenoptera: Formicidae). Aust. J. Zool. 16: 333-348 (page 344, see also)

References based on Global Ant Biodiversity Informatics

  • Brown W. L., Jr., and W. W. Kempf. 1960. A world revision of the ant tribe Basicerotini. Stud. Entomol. (n.s.) 3: 161-250.
  • Mann W. M. 1919. The ants of the British Solomon Islands. Bulletin of the Museum of Comparative Zoology 63:273-391.
  • Mann, W.M. 1919. The ants of the British Solomon Islands. Bulletin of the Museum of Comparative Zoology of Harvard College 63: 273-391
  • Taylor R. W. 1968. Notes on the Indo-Australian basicerotine ants (Hymenoptera: Formicidae). Australian Journal of Zoology 16: 333-348.
  • Taylor R. W. 1970. Notes on some Australian and Melanesian basicerotine ants (Hymenoptera: Formicidae). Journal of the Australian Entomological Society 9: 49-52.
  • Taylor R. W. 1980. Australian and Melanesian ants of the genus Eurhopalothrix Brown and Kempf - notes and new species (Hymenoptera: Formicidae). Journal of the Australian Entomological Society 19: 229-239.
  • Wheeler W.M. 1935. Check list of the ants of Oceania. Occasional Papers of the Bernice Pauahi Bishop Museum 11(11):1-56.
  • Wheeler, William Morton.1935.Checklist of the Ants of Oceania.Occasional Papers 11(11): 3-56