Pachyphymus namaquensis, Bazelet, Corinna S. & Naskrecki, Piotr, 2014
publication ID |
https://doi.org/ 10.11646/zootaxa.3753.5.1 |
publication LSID |
lsid:zoobank.org:pub:50DE53AD-6A51-4346-BD45-EF21F5E02C54 |
DOI |
https://doi.org/10.5281/zenodo.5672216 |
persistent identifier |
https://treatment.plazi.org/id/3545D538-FFC2-1B22-FF43-91E12B23FF6E |
treatment provided by |
Plazi |
scientific name |
Pachyphymus namaquensis |
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Pachyphymus cristulifer (Serville, 1838)
Figs. 2 View FIGURE 2 , 5E–L, 6E–I
Serville 1838: 692 >> Calliptamus cristulifer Walker 1870: 690 >> Caloptenus cristulifer
Martinez 1902: 261, 272 >> Euryphymus cristulifer Kirby 1910: 264 >> Acrotylus cristulifer
Uvarov 1922: 173 >> Pachyphymus cristulifer
Dirsh 1956: 132–136 >> Pachyphymus cristulifer Dirsh 1965: 258 >> Pachyphymus cristulifer
Diagnostic redescription (male, except where specified). Wings. Tegmen surpassing end of abdomen and hind knee but not excessively so. Hind wing infumation dark brown or black, covering 50–70% of wing, excluding wing interior but including apex; hind wing interior bright pink ( Figs. 6 View FIGURE 6 H–I). This species is most similar to P. namaquensis n. sp. but can be distinguished on the basis of the lower degree of hind wing infumation in the majority of specimens (compare Fig. 6 View FIGURE 6 I vs. 6A), and the pointier male cercus (Fig. 5H vs. 5N).
Abdomen. Supraanal plate transverse, with a longitudinal concavity in the middle, lateral margins upcurved; posterior margin of supraanal plate with two lateral and one large median projection; supraanal plate with pair of large, strongly sclerotized tubercles in center of basal half ( Figs. 2 View FIGURE 2 J–L). Apex of cercus elongate, terminating in point ranging from very sharp to blunted, descends and curves downwards into transverse curved ridge (Figs. 5E– L).
Phallic complex. Epiphallus with short ancorae and broad, lobiform apically blunt lophi ( Fig. 2 View FIGURE 2 M).
Female. Subgenital plate trilobate, with deep grooves separating lobes, large, pointed median lobe ( Figs. 2 View FIGURE 2 G– I).
Measurements. (♂ n=9, ♀ n=17)—body: ♂ 15.8–22.0, ♀ 21.3–25.7; pronotum: ♂ 2.5–4.2, ♀ 3.3–5.2; tegmen: ♂ 11.3–16.3, ♀ 15.3–19.7; femur: ♂ 7.7–10.0, ♀ 9.7–12.5 mm.
Material examined. South Africa: Eastern Cape: 13 mi N Miller Station (-33.0667, 23.9167) 12.ii.1958 —3♀, 2♂ ( SANC); 20 mi N Miller Station (-33.0667, 23.9167) 13.xii.1961 —1♀ ( SANC); 4 mi NW Miller Station (- 33.0667, 23.9167) 13.xii.1961 —2♀ ( SANC); 15 mi SW Graaf-Reinet (-32.2501, 24.5354) 14.xii.1961 —1♀ ( SANC); 7 mi S Graaf-Reinet (-32.2501, 24.5354) 12.xii.1960 —1♀ ( SANC); 18 mi E Touws River to Hondewater (-33.3378, 20.0336) xii.1962 coll. SAM museum expedition—2♀, 5♂ ( SAMC); 20 mi S Aberdeen (-32.4761, 24.0627) 16.xii.1961 —2♀, 1♂ ( SANC); 35 mi SW Aberdeen (-32.4761, 24.0627) 13.xii.1961 — 1♂ ( SANC); 9 mi W Klipplaat (-33.0200, 24.3408) 22.ii.1958 —5♀, 1♂ ( SANC); Steytlerville (-33.3273, 24.3447) 21.ii.1958 —1♀ ( SANC); Willowmore (-33.2916, 23.4904) 15.xi.1961 —1♀ ( SANC); Northern Cape: Bushmanland, “Lietjies Bos” xi.1935—1 ♀ ( SAMC); Middeldrift, 50 km S Calvinia (-31.4753, 19.7722) 1.iii.1969 — 1♂ ( SAMC); Wallekraal, Namaqualand (-30.3667, 17.5167)—1♀ ( SAMC); Western Cape: 26 mi NE Uniondale (-33.6587, 23.1231) 14.ii.1958 —1♀ ( SANC); 8 mi NE Touws River (-33.3378, 20.0336) xii.1962 coll. SAM museum expedition—3♀ ( SAMC); Waterford (-33.0791, 25.0089) 21.x.1961 —1♀ ( SANC); Richmond (-33.7272, 26.5733) iii.1931 coll. SAM museum expedition—1♀ ( SANC); Karoo, Klaarstroom, Prince Albert (-33.3306, 22.5344) x.1952 coll. SAM museum expedition—2♀ ( SAMC); Oudtshoorn “Zebra” (-33.4091, 22.5571) x.1951 coll. SAM museum expedition— 1♂ ( SAMC); Karoo, 3 mi SW Seekoegat (-33.0500, 22.5000) 12.xii.1961 coll. H.D. Brown, W. Furst, F. Pick—4♀, 2♂ ( SANC); 8 mi N Beaufort West (-32.3512, 22.5824) 5.xii.1961 —1♀, 1♂ ( SANC); Bulhoek Klaver, Clanwilliam (-32.0976, 19.0219)—1♀, 1♂ ( SAMC); Clanwilliam (-32.0976, 19.0219)— 1♂ ( SAMC); Leipoldtville (-32.2233, 18.4856) coll. SAM museum expedition—4♀, 1♂ ( SAMC); Leipoldtville, Eland’s Bay (- 32.2233, 18.4856) coll. SAM museum expedition—1♀, 4♂ ( SAMC); Olifants River btw. Citrusdal and Clanwilliam (-32.0976, 19.0219) coll. SAM museum expedition—1♀, 1♂ ( SAMC); Paleisheuwel (-32.4667, 18.7167) coll. SAM museum expedition—3♀, 2♂ ( SAMC); Uitpanskraal, 42 km NW Wuppertal (-32.2387, 19.1942) coll. SAM museum expedition— 1♂ ( SAMC).
Remarks. Specimens from Touwsrivier were distinct morphologically from the rest of the species. They were smaller ( Fig. 9 View FIGURE 9 E–F) had slightly different male cerci (Figs. 5G–H), variable female subgenital plate ( Fig. 2 View FIGURE 2 H), male supraanal plate ( Fig. 2 View FIGURE 2 K), and a slightly greater degree of infumation on the hind wing with a distinct border between the infumated and colorful areas of the wing ( Fig. 6 View FIGURE 6 H).
There was a distinct series of specimens from the region to the west of the Cederberg mountain range, from Leipoldtville, Eland’s Bay and Paleisheuwel to Wuppertal in the East (see GPS coordinates above). This group of specimens was the only one to exhibit variation in wing pattern and color. Wings varied from lightly to heavily infumated, with interior regions ranging from translucent to orange-pink to bright pink ( Figs. 6 View FIGURE 6 E–G). The geographic location of this group of organisms is relatively isolated by the Cederberg mountain range, and P. namaquensis is geographically more accessible than the majority of P. cristulifer . Wing color and infumation polymorphism is common in several species of Oedipodinae, particularly in association with soil coloration, presumably as a means of camouflage. While the same has not yet been shown for the Euryphyminae , it is possibly similar, and, therefore, wing pattern and coloration should only be used as a diagnostic character in association with other characters, particularly sexually selected ones. While there is slight variation in the other features of this population of P. cristulifer ( Figs. 2 View FIGURE 2 E–F, 2I, 2L, 5I –J) the variation falls within the threshold of normal intraspecific variation.
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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