Cyrtosathe kirkspriggsi Winterton & Metz
publication ID |
https://doi.org/ 10.5281/zenodo.171327 |
publication LSID |
lsid:zoobank.org:pub:A214C8D9-D5B9-4528-B64E-8CBDBF4357AB |
DOI |
https://doi.org/10.5281/zenodo.5686461 |
persistent identifier |
https://treatment.plazi.org/id/039787C2-D23B-FFD0-166A-FE0E5B75EB7E |
treatment provided by |
Plazi |
scientific name |
Cyrtosathe kirkspriggsi Winterton & Metz |
status |
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Cyrtosathe kirkspriggsi Winterton & Metz View in CoL gen. et sp. nov.
( Figs 1–4 View FIGURE 1 View FIGURE 2 View FIGURE 3 View FIGURE 4 )
Type species. Cyrtosathe kirkspriggsi sp. nov. by present designation.
Etymology. Cyrtosathe is derived from the Greek, cyrto, bent; sathe penis. The specific epithet is named in honour of Ashley KirkSpriggs, the collector of the type series.
Type material: Holotype male, NAMIBIA: Luderitz District, Ob[i]b Waters, pitfall trap (28°00’08”S, 16°36’46”), 10–26.viii.1998, KirkSpriggs & Marais (MEI#119440) ( NMNW). Paratypes, NAMIBIA: 2 males, 1 female, same data as holotype (MEI#119434, 119442, 119465) ( USNM); male, Obib Waters, Malaise trap (28°00’08”S, 16°38’46”) 25– 26.viii.1998, KirkSpriggs & Marais (MEI# 112932) ( USNM); 6 males, 1 female, Luderitz District, 8 km W Rosh Pinah, pitfall trap (27°59’28”S, 16° 39í14 ”) 20–26.viii.1998, Kirk Spriggs & Marais (MEI#119436, 119438, 119441, 119445–6, 119451, 119453) ( NMNW); 1 male, 1 female, Luderitz District, 8 km W Rosh Pinah, Malaise trap (27°59’28”S, 16°39’14”) 20–26.viii.1998, KirkSpriggs & Marais (MEI#119448, 119454) ( MEIC / CASC).
Diagnosis. Autapomorphic characters: Female tergite 8 covered with erect, elongate setae arranged in a ring pattern (i.e. glabrous centre); hypandrium bowllike with posterior processes; dorsal apodeme of parameral sheath enlarged into a ‘ladle’like structure enclosing ejaculatory apodeme; aedeagus folded onto itself posteriorly such that the ejaculatory apodeme is directed posteriorly. Shared characters with other genera: head and thorax mostly glabrous; costal vein ending just past R5; wing vein M2 present; hind coxal knob absent; abdominal tergite 2 sensory patch present as two hemispheres, sensory setae with apices acute (not truncated); male epandrium divided medially; hypandrium separate from gonocoxites; gonocoxal apodeme slightly longer than gonocoxites; distiphallus bifid, greatly elongate and narrow; ventral apodeme of parameral sheath absent.
Description. Body length: 2.0–2.5 mm. Head. Spherical, glossy dark brown to black; frons glabrous, narrow in male ( Figs 1 View FIGURE 1 A, B) with eyes contiguous along middle third, female ( Figs 1 View FIGURE 1 C, D) frons much wider than ocellar tubercle along entire length; male eyes with facets larger in upper half; ocellar tubercle raised, ocelli redbrown; occiput flat to slightly concave laterally; postocular ridge with irregular rows of minute postocular setae; gena with short setae; mouthparts brown, relatively elongate, approximately equal in length to antennae; labellum relatively small and rounded; antenna ( Fig. 1 View FIGURE 1 E) brown, overlain with fine silver pruinescence; scape and pedicel short, broad; flagellum 2x length of pedicel, flattened, apex pointed; style apical, single segment.
Thorax. Glossy black, glabrous except for fine, pale setae on katepisternum and short dark setae on proepimeron and scutellum; macrosetae absent; wing ( Fig. 2 View FIGURE 2 ) hyaline, venation pale, venation in posterior half of wing poorly sclerotised and difficult to detect; costal vein ending at R5 vein; vein M2 present, extending from middle of discal cell; haltere stem brown, knob pale creamwhite; legs dark brown to black, tibiae pale yellow, covered with fine pale setae.
Abdomen. Glossy black, sparsely covered with elongate, pale setae in male; tergite 2 with two medial hemispherical patches of sensory setae ( Fig. 1 View FIGURE 1 F).
Male Genitalia. Genitalia aligned with body axis (i.e. epandrium dorsal), not rotated; epandrium ( Figs 3 View FIGURE 3 A, C) quadrangular, arched, covering terminalia, split medially in two sections; cerci short, rounded; gonocoxites ( Figs 3 View FIGURE 3 B–C, E–F) elongate with spatulate posterior process and a short, strong seta dorsally; gonocoxites widely separated medially by a large rounded bowllike hypandrium; hypandrium with paired posterior processes and medial process ( Figs 3 View FIGURE 3 B–C, E–F); gonostylus elongate, narrow, apical third upturned slightly; gonocoxal apodeme elongate, equal to gonocoxite in length, curved outwards then recurved inwards at apex around dorsal apodeme of parameral sheath, apex spatulate; aedeagus extended anteriorly beyond gonocoxites, folded dorsally on itself, distiphallus bifid, greatly narrowed, elongate, slightly coiled, ribbonlike lateral flanges near base; dorsal apodeme of parameral sheath large, ‘ladle’shaped with lateral wings at base, cradling ejaculatory apodeme ( Figs 3 View FIGURE 3 B–E); lateral ejaculatory apodemes not clearly evident; ejaculatory apodeme narrow with greatly enlarged paddleshaped apex posteriorly.
Female Genitalia. Tergite 8 covered with erect, elongate pale setae arranged in a ringlike pattern (i.e. glabrous in the centre) ( Fig. 4 View FIGURE 4 A); tergite 9+10 joined to furca internally by a bridge formed by tergite 9 ( Figs 4 View FIGURE 4 B–C); acanthophorites with four to six stout A1 setae; furca ( Fig. 4 View FIGURE 4 C) circular, lightly sclerotised; sternite 8 bowl shaped; two spermathecae present; spermathecal ducts thickened basally, narrower distally, with reticulated tissue patterning; spermatheca membranous, truncated distally with thickened marginal band; spermathecal sac very small; spermathecae join to roof of bursa separately from and immediately posterior of spermathecal sac duct; accessory glands join to bursa just posterior to spermathecae.
Comments. Cyrtosathe kirkspriggsi gen. et sp. nov. is known from a single collecting locality in the Luderitz District, Namibia. All adults were collected by Malaise and pitfall traps. As with all other nonscenopinine window flies, the immature stages are unknown. The type series is only in fair condition as most specimens are shriveled, presumably when they were removed from alcohol and mounted.
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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