Oecobius thar, Tripathi & Sudhikumar & Sherwood, 2023
publication ID |
https://doi.org/ 10.11646/zootaxa.5389.4.6 |
publication LSID |
lsid:zoobank.org:pub:238A54F0-8539-4E8B-9CF2-EB7792137F5D |
DOI |
https://doi.org/10.5281/zenodo.10417374 |
persistent identifier |
https://treatment.plazi.org/id/03C087CA-D84D-CA56-FF2D-F4A09E6CB24C |
treatment provided by |
Plazi |
scientific name |
Oecobius thar |
status |
sp. nov. |
Oecobius thar sp. nov.
Figs 1–5 View FIGURE 1 View FIGURE 2 View FIGURE 3 View FIGURE 4 View FIGURE 5
Etymology. The specific name refers to the Thar Desert, where this species lives, and is a noun in apposition.
Type material. Holotype ♂ (NRC-AA-4153), INDIA: Rajasthan, Jaisalmer, Thar Desert, Sam area (26.8303°N, 70.5085°E). 235 m a.s.l., found on wall, collected by hand, 14 Aug. 2022, R. Tripathi coll. GoogleMaps Paratypes: same data as holotype, ♂ (NRC-AA-4154), ♀ (NRC-AA-4155) GoogleMaps .
Diagnosis. Oecobius thar sp. nov. most closely resembles O. cumbrecita Wunderlich, 1987 , O. fortaleza Wunderlich, 1992 and O. infierno Wunderlich, 1987 by the curved OTL ( Figs 2A–C View FIGURE 2 , 3 View FIGURE 3 ), however it can be distinguished by the apex of the OTL ending with three denticles ( Figs 2B–C View FIGURE 2 ), which are absent in O. cumbrecita , O. fortaleza and O. infierno . Females of O. thar sp. nov. can be distinguished by the triangle-shaped and heavily sclerotised epigyne ( Fig. 2D View FIGURE 2 , not triangle-shaped in all other known congeners).
Description. Male holotype: Colour (in alcohol): carapace and dorsal and lateral faces of palp dark brown; legs beige, with black annulation on all segments; opisthosoma overall dark brown (darker than carapace), dorso-lateral outermost quarters mottled with white blotches, dorso-medial area with foliate pattern at posterior extent, spinnerets and ventral face of the opisthosoma dark brown ( Fig. 1A–B View FIGURE 1 ). Total length 1.77. Carapace 0.75 long, 0.82 wide. Eyes: ALE 0.04, AME 0.06, PLE 0.08, PME 0.02, ALE–ALE 0.16, AME–AME 0.06, PLE–PLE 0.11, PME–PME 0.04. Opisthosoma 1.02 long, 0.68 wide. Legs: I 2.24 (0.68+0.13+0.50+0.51+0.42), II 2.51 (0.73+0.15+0.57+0.61 +0.45), III 2.55 (0.74+0.18+0.55+0.62+0.46), IV 2.69 (0.76+0.22+0.59+0.63+0.49). Palp: with massive oecobiid tegular lobe tapering strongly in proximal third, apex with three denticles, process present at base; embolus short; oecobiid tegular apophysis well-developed with two projections at apex, base with proximal process; membranous conductor present and rounded, anterior part of tegulum smooth and unmodified ( Figs 2A–C View FIGURE 2 , 3 View FIGURE 3 ).
Female paratype: Colour (in alcohol): carapace dark brown; legs beige and non-annulated; opisthosoma overall beige, overlain with black setae, dorso-median aspect with foliate pattern and two parallel black blotches, spinnerets and ventral face of opisthosoma mouse brown ( Fig. 1C–D View FIGURE 1 ). Total length 1.89. Carapace 0.66 long, 0.72 wide. Eyes: ALE 0.04, AME 0.06 PLE 0.07, PME 0.03, ALE–ALE 0.16, AME–AME 0.07, PLE–PLE 0.14, PME–PME 0.03. Opisthosoma 1.23 long, 0.79 wide. Legs: I 2.12 (0.67+0.14+0.48+0.43+0.40), II 2.36 (0.72+0.16+0.55+0.51+0.42), III 2.43 (0.75+0.19+0.51+0.57+0.41), IV 2.71 (0.71+0.22+0.63+0.75+0.40). Genitalia: epigyne triangle-shaped, sclerotised, with prominent proximal apex and widely spaced copulatory openings; copulatory atrium prominent, copulatory ducts twisted, each with an anterior diversion in the proximal third, copulatory ducts connecting at apex to asymmetrical globular spermathecae ( Figs 2D–E View FIGURE 2 ). We were unable to observe any fertilisation ducts, although cannot rule out their presence.
Colour in vivo. Typically as found in the (freshly) preserved specimens, although both male ( Fig. 4A–C View FIGURE 4 ) and female ( Fig. 4D View FIGURE 4 ) are more vibrant in respective colours.
Natural history. Oecobius thar sp. nov. exhibited a habitat preference consistent with a synanthropic lifestyle ( Fig. 4E View FIGURE 4 ). A large number of specimens were observed by RT on a residential wall, where female specimens constructed small sheet webs housing a cluster of eggs. They were observed to primarily predate ants and dipterans. During prey capture, the females employed a dynamic strategy, swiftly manoeuvring around their prey and utilizing a continuous silk-spinning technique to entrap and immobilize the target (RT pers. obs.). This behaviour is in no way unique, having been reported in several other congeners ( Glatz 1967; Voss et al. 2007; García et al. 2014; Líznarová et al. 2013; Líznarová & Pekár 2015).
Distribution. Known only from the type locality, in the Thar Desert ( Fig. 5 View FIGURE 5 ).
R |
Departamento de Geologia, Universidad de Chile |
No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.
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