Aphanostola rooiklipella Bidzilya & Mey, 2016
publication ID |
https://dx.doi.org/10.3897/dez.63.7556 |
publication LSID |
lsid:zoobank.org:pub:542B0277-F899-48ED-8387-EE760EEEF5A4 |
persistent identifier |
https://treatment.plazi.org/id/6E6F7B55-91F7-4807-A91E-26DAC7A50B24 |
taxon LSID |
lsid:zoobank.org:act:6E6F7B55-91F7-4807-A91E-26DAC7A50B24 |
treatment provided by |
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scientific name |
Aphanostola rooiklipella Bidzilya & Mey |
status |
sp. n. |
Aphanostola rooiklipella Bidzilya & Mey sp. n. Figs 16 View Figures 1–21 , 51 View Figures 47–52 , 70 View Figures 68–70 , 71 View Figures 71–73 , 71a View Figures 71–73
Type material.
Holotype ♀, Namibia, Gamsb[er]g., Rooiklip Farm, 10-11.ix.20012, LF (Mey) ( MfN). Paratypes: 8 ♀, same data as holotype (gen. slide 495/14; 547/14; 554/14, O. Bidzilya); 1 ♀, Namibia, Rooisand, Gamsberg Pass, 20.i.2007, aut[omatische] Falle (Mey & Ebert) (gen. slide 203/12, O. Bidzilya); 1 ♂, 1 ♀, Namibia, Omatako Ranch, LF, 22-23.iii.2003 (Mey) (gen. slide 213/12♂, 66/15♀, O. Bidzilya); 1 ♀, Namibia, Otjiwarongo, Hohenfels, 25-27.viii.2012, LF (Mey) (gen. slide 561/14, O. Bidzilya) ( MfN); 1 ♀, RSA, Natal, Mkuzi, [15'sq NW cnr, 27 30'S, 32 05'E], 23-26.iv.1982 (Scoble, Laurenson & Kroon) (gen. slide 45/15, O. Bidzilya) ( TMSA).
Diagnosis.
The new species can reliably be separated from Aphanostola melliferae sp. n. and Aphanostola africanella sp. n. by the genitalia. The male genitalia most resemble those of Aphanostola acaciae sp. n., but are well recognizable by the presence of the big rounded lateral, vincular projections in combination with sub-rectangular tegumen and apically tapered phallus. The female genitalia resemble those of Aphanostola griseella sp. n., but the antrum is distinctly longer than the apophyses anteriores in Aphanostola rooiklipella sp. n. whereas the antrum in Aphanostola griseella sp. n. is sub-equal in length to apophyses anteriores; moreover the sub-ostial sclerite in Aphanostola griseella sp. n. is shorter and having shorter posterior projections.
Description.
Adult (Fig. 16 View Figures 1–21 ). Wingspan 6.2-6.4 mm. Head, thorax and tegulae covered with grey black-tipped scales, frons off-white, labial palpus weakly up-curved, segment two black with whitish scales at base, segment three black with white basal, medial and apical rings, inner surface lighter, greyish, antenna thick in male, thin in female, finely ciliated in both sexes, scape black, other antennal segments black with narrow whitish rings at base, underside greyish; forewing light grey densely suffused with brown along margins and particularly on apex, three prolonged brown spots in cell, diffuse brown dash in fold, cilia grey, brown-tipped; hindwing grey.
Male genitalia (Fig. 51 View Figures 47–52 ). Uncus about as broader as long, weakly widened apically, posterior margin slightly emarginated; gnathos sickle-shaped; tegumen sub-rectangular, 1.5 times longer than broad, anterior margin with comparatively shallow, rounded emargination; valva straight, inner margin with distinct thorn at 2/3 length, distal 1/3 inflated, hairy; sacculus prolonged, narrow, curved inwardly; vinculum narrow, posterior margin with short medial and long lateral projections, anteromedial emargination shallow; saccus broad, triangular, slightly exceeding beyond apex of pedunculus; phallus with pointed apex, basal projection arises from 1/3 length of phallus and exceeding nearly to its tip.
Female genitalia (Figs 70 View Figures 68–70 , 71 View Figures 71–73 , 71a View Figures 71–73 ). Segment VIII nearly as long as broad, evenly sclerotized; apophyses anteriores moderately thick, twice as long as segment VIII; antrum long, tubular, exceeding the tips of apophyses anteriores; sub-ostial sclerite sub-rectangular with long posterior projection; ductus bursae narrow; corpus bursae sub-ovate; signum a long sub-triangular plate densely covered with spikes and with medial cord inside.
Etymology.
Named after the farm Rooiklip in the escarpment of Namibia.
Distribution.
Namibia.
Biology.
The host plant unknown. The adults were observed from late August to mid-September, and again in January and in March, which is suggestive for the development of two generations per year.
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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