Research Article |
Corresponding author: Oleksiy V. Bidzilya ( olexbid@gmail.com ) Academic editor: Dominique Zimmermann
© 2016 Oleksiy V. Bidzilya, Wolfram Mey, David Agassiz.
This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Citation:
Bidzilya OV, Mey W, Agassiz D (2016) Review of the genus Aphanostola Meyrick, 1931 (Lepidoptera, Gelechiidae, Anomologinae) with description of 19 new species from the Afrotropical Region. Deutsche Entomologische Zeitschrift 63(1): 45-74. https://doi.org/10.3897/dez.63.7556
|
New diagnosis of the genus Aphanostola is provided, and its position within Gelechiidae is briefly discussed. 19 species are described from South Africa, Namibia, Botswana, Zimbabwe, Tanzania, Kenya and Ethiopia: A. acaciae Bidzilya & Mey, sp. n., A. morogorensis Bidzilya, sp. n., A. calderae Bidzilya & Mey, sp. n., A. kenyella Bidzilya & Agassiz, sp. n., A. kruegeri Bidzilya & Mey, sp. n., A. alternella Bidzilya & Agassiz, sp. n., A. antennata Bidzilya & Mey, sp. n., A. rooiklipella Bidzilya & Mey, sp. n., A. griseella Bidzilya & Mey, sp. n., A. centripunctella Bidzilya & Mey, sp. n., A. joannoui Bidzilya & Mey, sp. n., A. namibiensis Bidzilya & Mey, sp. n., A. brandbergensis Bidzilya & Mey, sp. n., A. aarviki Bidzilya, sp. n., A. africanella Bidzilya, Agassiz, & Mey, sp. n., A. emarginata Bidzilya & Mey, sp. n., A. melliferae Bidzilya, Agassiz & Mey, sp. n., A. maxima Bidzilya & Mey, sp. n., A. longicornuta Bidzilya, Agassiz & Mey, sp. n. A key to the species is given based on external characters and the genitalia of both sexes. Adults and genitalia of all species are illustrated.
Lepidoptera , Gelechiidae , Aphanostola , new species, taxonomy, host plants, Afrotropical region, Oriental region
The genus Aphanostola was originally established for two species: A. atripalpis Meyrick, 1931 (type species) and A. sparsipalpis Meyrick, 1931. Later A. intercepta Meyrick, 1932 was added to this genus. The latter two species are only known from single males without abdomens, therefore their generic assignment with Aphanostola remains rather obscure.
As a result of our study of the Gelechiidae from the Brandberg Massif in Namibia, a number of small-sized specimens that represent a separate group consisting of four species have been discovered. Their genitalia matched in most details to the genitalia of Lanceopenna pentastigma Janse, 1960. It was realized however that L. pentastigma is not congeneric with L. pseudogaleotis Janse, 1950 – the type species of Lanceopenna Janse, 1950, but better fits in genitalia characters to A. atripalpis from India (
The recent examination of the holotype and male paratype of A. atripalpis confirmed the assumption that specimens from the Brandberg are indeed congeneric with Aphanostola. Moreover, a number of additional species from this genus have been found in collections of material from southern Africa and other countries of the Afrotropical region since 2007. Some of these species were mentioned as new but not formally described in recent papers (
The aim of the present paper is to describe new species, which were found belonging to Aphanostola. A total of 19 new species are described and an improved and expanded diagnosis of the genus Aphanostola within the subfamily Anomologinae is provided.
The present paper is based mainly on material from
The genitalia slides were prepared according to the “unrolling technique” (
In the paragraph “Material” of the descriptions the localities were arranged geographicly from south-west to north-east and countries are referred to using their current names.
A. acaciae Bidzilya & Mey, sp. n.
A. pentastigma (Janse, 1960)
A. morogorensis Bidzilya, sp. n.
A. calderae Bidzilya & Mey, sp. n.
A. kenyella Bidzilya & Agassiz, sp. n.
A. kruegeri Bidzilya & Mey, sp. n.
A. alternella Bidzilya & Agassiz, sp. n.
A. antennata Bidzilya & Mey, sp. n.
A. rooiklipella Bidzilya & Mey, sp. n.
A. griseella Bidzilya & Mey, sp. n.
A. centripunctella Bidzilya & Mey, sp. n.
A. joannoui Bidzilya & Mey, sp. n.
A. namibiensis Bidzilya & Mey, sp. n.
A. brandbergensis Bidzilya & Mey, sp. n.
A. aarviki Bidzilya, sp. n.
A. africanella Bidzilya, Agassiz & Mey, sp. n.
A. emarginata Bidzilya & Mey, sp. n.
A. melliferae Bidzilya, Agassiz & Mey, sp. n.
A. maxima Bidzilya & Mey, sp. n.
A. longicornuta Bidzilya Agassiz & Mey, sp. n.
A. atripalpis Meyrick, 1931
A. sparsipalpis Meyrick, 1931
A. intercepta Meyrick, 1932
Exotic Microlepidoptera 4: 56
Aphanostola atripalpis Meyrick, 1931 (by original designation).
The genus Aphanostola is defined by the combination of the following characters in the male genitalia (Fig.
The male genitalia of Aphanostola display similarity to the genitalia of Leuronoma Meyrick, 1918 and Platyphala Janse, 1951. These genera share such characters as a weakly sclerotized distal portion of the valva, the sacculus strongly curved inwardly and the inner margin of the valva with tendency to form a thorn. The adults of all three genera are characterized by sexual dimorphism in the width of the antenna. The monotypic genus Platyphala seems to be more closely related to Aphanostola in having the phallus with short basal projection, but differs in the prolonged uncus without long setae and the shorter gnathos. The diagnosis of Leuronoma is unclear as the type species (L. chlorotoma Meyrick, 1918) lacks the abdomen and its affiliation with of the other species is rather provisional. Most of the species currently associated with Leuronoma differ from Aphanostola species in the uncus which is deeply divided into two lobes, the reduced saccus and a differently shaped phallus. Aphanostola, Platyphala and Leuronoma along with several unrevised groups of species form a separate branch within the tribe Anomologini (subfamily Anomologinae) remotely related to Aristotelia Hübner, [1825].
Based on the above diagnosis 23 species are considered here to be members of Aphanostola. However, there is a group of still undescribed species which takes an intermediate position among Aphanostola, Leuronoma and Platyphala. It is possible that the current diagnosis of Aphanostola must be expanded and additional species have to be included resulting from future revisions of related genera.
Head smoothly scaled, ocelli absent, grey or brown sometimes white (A. brandbergensis sp. n.). Labial palpus straight or weakly up-curved, segment 2 slightly broader than segment 3, segment 3 acute, about as wide as segment 2; antenna of male slightly thicker and more distinctly ciliated than antenna of female in most of species (A. calderae sp. n., A. longicornuta sp. n., A. rooiklipella sp. n., A. griseella sp. n.), scape without pecten, antennal segments grey to brown with black rings at base.
Thorax grey to brown; wingspan 5.8–10.5 mm; forewing usually pale, grey, or light brown, sometimes whitish or yellowish with brown base of costal margin (A. calderae sp. n., A. morogorensis sp. n., A. brandbergensis sp. n., A. aarviki sp. n.), three diffuse dark spots in cell, margins often mottled with black appearing darker than medial part of wing, some species with additional black spots at base and on ¾ of dorsum (A. morogorensis sp. n.). Hindwing grey, with well developed tornal excavation and pointed tip.
Male tergum VIII sub-rectangular, usually broader than long, strongly edged and weakly emarginated anteriorly; sternum VIII broader than long, posterior margin broadly rounded, anteriolateral corners projected, sometimes strongly. Female segment VII trapezoidal, tergum VIII about twice length of other abdominal segments, sternum VIII three times longer than broad; sternum II of both sexes with pair of venulae, apodemes well developed.
Male genitalia (Fig.
Female genitalia (Fig.
Afrotropical (South Africa, Zimbabwe, Namibia, Botswana, Kenya, Tanzania, Ethiopia) and Oriental (India) regions.
A. pentastigma, A. acaciae sp. n., A. africanella sp. n. and A. melliferae sp. n. were reared from various Acacia-species in Kenya (
In the southern Africa the adults were observed from late August to early May, up to 2000 m elevation in Auas Mts and Brandberg, easily attracted to light. In East Africa adults fly from August to January up to 1850 m elevation.
(Note: A. joannoui sp. n., A. antennata sp. n., A. longicornuta sp. n., A. alternella sp. n. and A. rooiklipella sp. n., A. melliferae sp. n.,. A. africanella sp. n. can hardly be distinguished from each other without examination of the genitalia)
1 | Wingspan 9.5–10.5 mm, forewing light brown with brown dots | A. maxima sp. n. |
– | Wingspan less than 9.5 mm | 2 |
2 | Forewing white with distinct black markings | A. acaciae sp. n |
– | Forewing otherwise coloured | 3 |
3 | Forewing yellow, black markings large | 4 |
– | Forewing grey, light brown, cream or light yellow, black markings usually small | 5 |
4 | Black spot on ¾ of dorsum large, forewing comparatively narrow, 7.1 mm | A. morogorensis sp. n. |
– | Black spot on ¾ small, forewing comparatively broad, 6.2 mm | A. aarviki sp. n. |
5 | Forewing light yellow or cream-white | 6 |
– | Forewing grey | 7 |
6 | Forewing light yellow, costal margin without black irroration, 7.1–7.5 mm | A. calderae sp. n. |
– | Forewing cream-white, costal margin with black irrorartion, 5.8–6.1 mm | A. brandbergensis sp. n. |
7 | Forewing with large brown, transverse spot in middle | A. centripunctella sp. n. |
– | Forewing without large brown, transverse spot in middle | 8 |
8 | Wingspan 8.0–9.1 mm | 9 |
– | Wingspan less than 8.0 mm | 10 |
9 | Forewing black-brown without markings, head brown, 8.0–8.2 mm | A. kenyella sp. n. |
– | Forewing grey with rounded black spot in middle, head white, 9.0–9.1 mm | A. namibiensis sp. n. |
10 | Forewing long and narrow, with four black spots in cell and three black spots on costal margin | A. pentastigma |
– | Forewing shorter and broader | 11 |
11 | Forewing light brown | 12 |
– | Forewing grey | 13 |
12 | Forewing densely mottled with black irroration | A. kruegeri sp. n. |
– | Forewing without black irroration | A. emarginata sp. n. |
13 | Forewing uniformly grey | A. atripalpis |
– | Forewing with black markings | 14 |
14 | Forewing comparatively dark, grey | A. joannoui sp. n., A. antennata sp. n., A. longicornuta sp. n., A. alternella sp. n. |
– | Forewing comparatively light grey, with white pattern | |
15 | Forewing uniformly grey except of margins mottled with black | A. griseella sp. n. |
– | Forewing with black markings in cell | A. rooiklipella sp. n., A. melliferae sp. n., A. africanella sp. n. |
(Note: The male of A. griseella sp. n. is unknown)
1 | Projection of phallus present | 2 |
– | Projection of phallus absent | 13 |
2 | Vesica with one long cornutus, lateral vincular projections very long | A. longicornuta sp. n. |
– | Vesica with several small cornuti or without cornutus, lateral vincular projections short or absent | 3 |
3 | Phallus as long as or slightly longer than saccus | A. antennata sp. n. |
– | Phallus twice as long as saccus | 4 |
4 | Projection of phallus very short, reaching 1/5 of its length | A. kruegeri sp. n. |
– | Projection of phallus long, reaching at least ¾ of its length | 5 |
5 | Tooth on inner margin of valva situated close to sacculus and joined on base | 6 |
– | Tooth on inner margin of valva situated more distally from sacculus | 8 |
6 | Phallus with apical tooth | A. kenyella sp. n. |
– | Phallus without apical tooth | 7 |
7 | Tooth on inner margin of valva about as long as sacculus | A. centripunctella sp. n. |
– | Tooth on inner margin of valva much shorter than valva | A. alternella sp. n. |
8 | Sacculus twice as broad as valva in middle | A. joannoui sp. n. |
– | Sacculus as broad or narrower than valva in middle | 9 |
9 | Lateral vincular projections large, rounded, phallus strongly pointed apically | A. rooiklipella sp. n. |
– | Lateral vincular projections small or absent, phallus not pointed apically or gradually tapered | |
10 | Phallus serrated laterally in distal portion | 11 |
– | Phallus not serrated in distal portion | 12 |
11 | Saccus rounded apically, process of phallus broadened at apex, vesica with small cornuti | A. acaciae sp. n. |
– | Saccus pointed apically, process of phallus not broadened at apex, vesica without cornuti | A. calderae sp. n. |
12 | Saccus long, subrectangular, process of phallus arising from 1/3 of its length | A. morogorensis sp. n. |
– | Saccus triangular, process of phallus arising from about middle of phallus | A. pentastigma |
13 | Uncus covered with short setae | A. atripalpis |
– | Uncus covered with long setae | 14 |
14 | Vesica with 7–9 cornuti | A. africanella sp. n. |
– | Vesica without cornuti | 15 |
15 | Saccus stout, broadly rounded | A. melliferae sp. n. |
– | Saccus smaller | 16 |
16 | Tegumen broad, trapezoid, sacculus sub-rectangular | A. maxima sp. n. |
– | Tegumen narrow, elongate sub-rectangular | 17 |
17 | Saccus comparatively long, pointed apically, sacculus very short, hump-shaped | A. emarginata sp. n. |
– | Saccus comparatively short, rounded, sacculus longer | 18 |
18 | Sacculus narrow, long, uncus longer than broad | A. namibiensis sp. n. |
– | Sacculus broader and shorter, uncus broader than long or rounded | 19 |
19 | Uncus rounded, sacculus strongly pointed, phallus without apical thorn | A. aarviki sp. n. |
– | Uncus heart-shaped, sacculus weakly pointed, phallus with single apical thorn | A. brandbergensis sp. n. |
(Note: The females of A. calderae sp. n., A. kenyella sp. n., A. emarginata sp. n., A. aarviki sp. n., A. maxima sp. n., A. alternella sp. n. are unknown; the female of A. atripalpis has not been examined.)
1 | Signum present | 2 |
– | Signum absent | 8 |
2 | Antrum longer than half length of apophyses anteriores | 3 |
– | Antrum shorter than half length of apophyses anteriores | 5 |
3 | Signum a prolonged plate with small teeth | A. africanella sp. n. |
– | Sigmum a prolonged plate covered with spikes and with cord inside | 4 |
4 | Antrum distinctly longer than apophyses anteriores, subostial sclerite with posterior projection | A. rooiklipella sp. n. |
– | Antrum sub-equal in length to apophyses anteriores, subostial sclerite without posterior projection | A. griseella sp. n. |
5 | Signum a large, rounded plate with numerous spikes | A. morogorensis sp. n. |
– | Signum of another shape | 6 |
6 | Signum brush-shaped, corpus bursae large, rounded; subostial sclerite big, of irregular shape | A. centripunctella sp. n. |
– | Signum a weakly curved, narrow plate, corpus elongated; subostial sclerite narrow | A. kruegeri sp. n. |
7 | Ductus bursae coiled, posterior portion weakly wrinkled, signum a prolonged plate with serrated margins | A. longicornuta sp. n. |
– | Ductus bursae not coiled and without wrinkles, signum a spinose plate | A. antennata sp. n. |
8 | Ductus bursae with short appendix | A. acaciae sp. n. |
– | Ductus bursae without appendix | 9 |
9 | Corpus bursae covered with numerous spikes | A. pentastigma |
– | Corpus bursae without spikes | 10 |
10 | Ductus bursae with sclerotized band | A. melliferae sp. n. |
– | Ductus bursae without sclerotized band | 11 |
11 | Subostial sclerite absent | A. brandbergensis sp. n. |
– | Subostial sclerite present | 12 |
12 | Sternum VIII with sclerotized patches arising from base of apophyses anteriores, subostial sclerite digitate | A. namibiensis sp. n. |
– | Sternum VIII without sclerotized patches, subostial sclerite a transverse prolonged plate | A. joannoui sp. n. |
Genus 1, sp. 1. –
Aphanostola sp. 1 –
Holotype ♂, [Namibia] 20 km NW Uis, LF, 27.ii.2002 (Turm) (Mey) (gen. slide 101/05, O. Bidzilya) (
The species is recognizable externally by the white or light grey forewing with a black dash at base of costa, two black dashes at base of fold and three distinct black spots in cell. The male genitalia differ from the rest of Aphanostola species in the very short uncus in combination with apically narrowed saccus, the long, strongly curved gnathos, the basal projection of the phallus broadened at apex and the presence of small cornuti in the vesica. The female genitalia can be recognized unmistakably by the shape of the antrum and by the broad ductus bursae bearing a lateral appendix.
Adult (Figs
Adults of Aphanostola spp. (scale bar 1.0 mm) 1. A. acaciae sp. n., Namibia, Brandberg (gen. slide 73/05); 2. A. acaciae sp. n., Namibia, Mirabib (gen. slide 548/14); 3. A. acaciae sp. n., Kenya, Logumgum (gen. slide 1362); 4. A. pentastigma, HT, RSA, Pretoria; 5. A. pentastigma, Kenya, L. Naivasha; 6. A. morogorensis sp. n., HT, Tanzania, Morogoro Town; 7. A. calderae sp. n., RSA, Asante-Sana; 8. A. calderae sp. n., HT, RSA, Asante-Sana; 9. A. kenyella sp. n., Kenya, between Limuru and Mai Mahiu (gen. slide 1497); 10. A. kenyella sp. n., HT, Kenya, between Limuru and Mai Mahiu; 11. A. kruegeri sp. n., RSA, Pretoria (gen. slide 8/15); 12. A. alternella sp. n., HT, Kenya, Turi; 13. A. antennata sp. n., HT, Namibia, Popa Falls; 14. A. antennata sp. n., RSA, Nwanedzi (gen. slide 36/15); 15. A. antennata sp. n., Namibia, Kavango; 16. A. rooiklipella sp. n., HT, Namibia, Rooiklip Farm; 17. A. griseella sp. n., HT, Namibia, Grootfontein; 18. A. griseella sp. n., Kenya, Nakuru NP (gen. slide 596/14); 19. A. centripunctella sp. n., Namibia, E. Caprivi (gen. slide 76/05); 20. A. centripunctella sp. n., Namibia, E. Caprivi; 21. A. centripunctella sp. n., Namibia, E. Caprivi (gen. slide 155/15).
Variation. Ground colour of forewing varies from white to light grey.
Male genitalia (Figs
Adults of Aphanostola spp. (scale bar 1.0 mm) 22. A. joannoui sp. n., HT, RSA, Hongonyi Lodge; 23. A. joannoui sp. n., RSA, Hongonyi Lodge (209/12); 24. A. namibiensis sp. n., HT, Namibia, Brandberg; 25. A. namibiensis sp. n., Namibia, Auas Mts.; 26. A. brandbergensis sp. n., Namibia, Brandberg (gen. slide 74/05); 27. A. aarviki sp. n., HT, Tanzania, Morogoro Town; 28. A. africanella sp. n., Namibia, Mt. Etjo (gen. slide 597/14); 29. A. africanella sp. n., Namibia, E. Etosha (gen. slide 151/15); 30. A. africanella sp. n., Kenya, Baringo; 31. A. emarginata sp. n., HT, RSA, Mkuzi; 32. A. melliferae sp. n., Kenya, L. Bogoria (gen. slide 143/15); 33. A. melliferae sp. n., HT, Kenya, L. Bogoria; 34. A. maxima sp. n., Ethiopia, Tana-See; 35. A. maxima sp. n., HT, Ethiopia, Tana-See; 36. A. longicornuta sp. n., Kenya, L. Bogoria (gen. slide 577/14); 37. A. longicornuta sp. n., Kenya, Kakamega Forest (gen. slide 590/14); 38. A. longicornuta sp. n., Kenya, Kakamega Forest; 39. A. atripalpis, PT, India, Pusa (gen. slide 411/14).
Male genitalia of Aphanostola spp. 41. A. acaciae sp. n., HT, Namibia, 20 km NW Uis (gen. slide 101/05); 42. A. acaciae sp. n., Namibia, Rooiklip Farm (gen. slide 496/14); 43. A. pentastigma, Kenya, L. Naivasha (gen. slide 1357); 44. A. morogorensis sp. n., HT Tanzania, Morogoro Town (gen. slide 2378); 45. A. calderae sp. n., HT, Namibia, Asante-Sana (gen. slide 184/12); 46. A. calderae sp. n., Namibia, Asante-Sana (582/14).
Variation. Uncus sometimes reduced to short, paired hump.
Female genitalia (Fig.
The specific epithet refers to the hostplant, Acacia tortilis, of the new species.
South Africa, Namibia, Zimbabwe, Kenya.
The larva feeds on Acacia tortilis (Forssk.) Hayne (Fabaceae) in Kenya (
Lanceopenna pentastigma Janse, 1960 – Moths of South Africa, 6 (2): 216, pl. 105, pl. 109f, pl. 121e, pl. 118 h, i.
Aphanostola pentastigma (Janse, 1960) –
Holotype of L. pentastigma, ♀, [South Africa], Pretoria, 28.viii.1937 (Vári) (gen. slide. 8394), L. pentastigma Janse, ♀, Holotype No: 3684. Paratypes: ♂, Pretoria, 30.x.1948 (Vári) (gen. slide 8781), 2 ♂, Gladde Klipkop, 1–9.iii.1954 (Janse) (gen. slide 254/12, O. Bidzilya); 1 ♀, Pretoria, 20.x.1952 (Vári) (gen. slide 260/12, O. Bidzilya); 1 ♀, Pretoria, 10.i.1951 (Vári); 1 ♂, Pretoria, 21.viii.1949 (Vári); 1 ♂, Pretoria, 15.viii.1953, e.l. Acacia sp. (Vári); 1 ♂, Pretoria, 8.i.1975 (Vári) (gen. slide 32/15, O. Bidzilya); 1 S, Pafuri, K.N.P. Survey, 8.v.1975 (Potgieter & Scoble) (gen. slide 44/15, O. Bidzilya) (all
L. pentastigma is recognizable externally by the narrow, prolonged forewing with four black spots in cell and two black spots on costal margin. The male genitalia resemble those of A. acaciae sp. n., but the uncus is longer, the saccus is narrower, the phallus lacks cornuti and teeth, and the basal projection is shifted nearly to the middle. The female genitalia differ from the other Aphanostola species in the presence of numerous spikes on the wall of the corpus bursae.
Adult (Figs
Male genitalia (Fig.
Female genitalia (Figs
Variation. The specimens from Kenya have no teeth on the wall of the corpus bursae, only spikes are present, and their number is much smaller than in females from South Africa; the corpus bursae is distinctly smaller too, the ductus bursae is broader, the transition to the corpus bursae is more gradual.
South Africa, Zimbabwe, Kenya.
Larva feeds on Acacia xanthophloea Benth. (Fabaceae) in Kenya (
Lanceopenna pentastigma was described from nine specimens of both sexes collected in South Africa and Zimbabwe. We were able to examine the type series. The genitalia of both sexes match well with those of Aphanostola, therefore the species was transferred to this genus (Bidzilya and Agassiz 2016 in press).
The specimens from Kenya agree well externally with specimens from the type series and also in the male genitalia, but differ in some details in the female genitalia (see above). However, we do not consider these to be separate species.
Holotype ♂, Tanzania, Morogoro, Morogoro Town, 20.ix.1992 (Aarvik) (gen. slide 2378, O. Bidzilya) (MNHO). Paratype: 1 ♀, same data as holotype but 13.ix.1992 (gen. slide 2375, O. Bidzilya) (MNHO).
The new species is very similar externally to A. aarviki sp. n., but larger, the forewing is narrower and black spot on ¾ of dorsum is larger. The male genitalia are most close to those of A. acaciella sp. n. but differ in the longer saccus, the bigger vincular projections, a slenderer phallus and in other details. The female genitalia remotely resemble those of A. africanella sp. n., but the antrum is not developed and the signum is larger, rounded rather than elongated.
Adult (Fig.
Male genitalia (Fig.
Female genitalia (Fig.
The name refers to the type locality.
Tanzania.
The host plant is unknown. The adults have been collected in September.
Holotype ♂, [South Africa], RSA, East.[ern] Cape, Sneeuberg [area], Asante-Sana, 2.-6. iv.2011 (Mey) (gen. slide 184/12, O. Bidzilya) (
The new species is well recognizable externally by the yellow-white forewing with black markings. The male genitalia resemble those of A. acaciae sp. n. but differ in the longer uncus, the inner margin of the valva bearing a medial thorn, the sacculus not constricted before apex, the triangular saccus, and the shorter process of the phallus.
Adult (Figs
Male genitalia (Figs
Female. Unknown.
The name refers to the location of the game farm Asante Sana in the escarpment, where the landscape is reminiscent of a caldera.
South Africa.
Host plant unknown. Adults were collected late January and early April.
Holotype ♂, Kenya, Central, Escarpment, between Limuru and Mai Mahiu, 01°02’09”S, 36°35’58” E, 1850 m, M.V., light, 14.viii.1999 (Agassiz) (gen. slide 578/14, O. Bidzilya) (coll. Agassiz). Paratype: ♂, same data as holotype (gen. slide 1497, O. Bidzilya) (coll. Agassiz).
A. kenyella sp. n. is recognizable externally by the dark, nearly entirely black forewing and comparatively large size. The male genitalia are characterized by the broad sacculus, the narrow saccus and the phallus with distinct lateral teeth on the tip.
Adult (Figs
Variation. Forewing, head and thorax varies from those of described above to dark, nearly uniformly black.
Male genitalia (Fig.
Male genitalia of Aphanostola spp. 47. A. kenyella sp. n., Kenya, between Limuru and Mai Mahiu (gen. slide 1497); 48. A. kruegeri sp. n. , RSA, Pretoria (gen. slide 4/15); 49. A. alternella sp. n., HT, Kenya, Turi (gen. slide 307/14); 50. A. antennata sp. n., Namibia, Popa Falls (gen. slide 54/08); 51. A. rooiklipella sp. n., Namibia, Omatako (gen. slide 213/12); 52. A. centripunctella sp. n., Namibia, Brandberg (gen. slide 106/05).
Female. Unknown.
The species name refers to the country of occurrence of the new species.
Kenya.
Host plant unknown. The specimens from the type-series were collected in mid-August at 1850 m elevation.
Holotype ♀, [South Africa] Pretoria, 1.ii.1951 (Vári) (gen. slide 8/15, O. Bidzilya) (
The new species is externally very similar to A. emarginata sp. n. in having brown forewing, but the forewing is densely black irrorated. The male genitalia are defined by the very short basal projection of the phallus. The elongated narrow subostial sclerite and the narrow signum are characteristic for the female genitalia.
Adult (Fig.
Variation. Some specimens with blackish dorsal margin of forewing.
Male genitalia (Fig.
Female genitalia (Fig.
The species is dedicated to Martin Krüger, Lepidoptera curator in the
South Africa.
The host plant is unknown. The adults were collected in October, January and February.
Holotype ♂, Kenya, Rift valley, Turi, 8000ft, 11.iii.2000 (Agassiz) (gen. slide 307/14 (=1538), O. Bidzilya) (coll. Agassiz).
The new species can be reliably separated from A. joannoui sp. n., A. antennata sp. n. and A. longicornuta sp. n. by the study of the genitalia. The male genitalia are most similar to those of A. kruegeri sp. n. but the sacculus is longer, the gnathos is narrower and the basal projection of the phallus is longer than in the mentioned species.
Adult (Fig.
Male genitalia (Fig.
Female. Unknown.
The specific name is derived from “alternarius” (Latin), alternating, which refers to the alternating brown and white rings of the antenna.
Kenya.
The host plant is unknown. The adult moth was collected in March at an altitude of 2400 m.
Aphanostola sp. –
Holotype ♂, NAMIBIA-Exp.,
The new species can be reliably separated from A. joannoui sp. n., A. longicornuta sp. n., and A. alternella sp. n. by comparing the genitalia. The males can be recognized further by the extremely thickened antennae. The male genitalia are similar to those of A. calderae sp. n., but can be easily recognized by the short phallus, the short postero-medial incison of the vinculum and the more prolonged tegumen. The female genitalia are characterized by the unique spinose signum and V-shaped antrum.
Adult (Figs
Male genitalia (Fig.
Female genitalia (Fig.
The specific name refers to the thickened antenna of the male.
South Africa, Namibia.
Host plant unknown. Adults occur from November to December and from February to early May.
Holotype ♀, Namibia, Gamsb[er]g., Rooiklip Farm, 10–11.ix.20012, LF (Mey) (
The new species can reliably be separated from A. melliferae sp. n. and A. africanella sp. n. by the genitalia. The male genitalia most resemble those of A. 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 A. griseella sp. n., but the antrum is distinctly longer than the apophyses anteriores in A. rooiklipella sp. n. whereas the antrum in A. griseella sp. n. is sub-equal in length to apophyses anteriores; moreover the sub-ostial sclerite in A. griseella sp. n. is shorter and having shorter posterior projections.
Adult (Fig.
Male genitalia (Fig.
Female genitalia (Figs
Named after the farm Rooiklip in the escarpment of Namibia.
Namibia.
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.
Holotype ♀, NAMIBIA-Exp.,
The species is very similar externally to A. rooiklipella sp. n., A. africanella sp. n. and A. melliferae sp. n., but can be defined by the nearly uniformly grey forewing with poorly expressed black markings in cell. The female genitalia most closely resemble those of A. rooiklipella sp. n. - for the differences see under that species.
Adult (Figs
Male. Unknown.
Female genitalia (Figs
Derived from “griseus” (Latin), grey, referring to the grey forewings.
South Africa, Namibia, Kenya.
The host plant is unknown. The adults were observed in October-November and again in February-March.
Genus 1, sp. 2. –
Holotype ♂, NAMIBIA-Exp.,
The new species is well recognizable externally by the comparatively large size and the forewing with a large brown spot in the middle. The external differences to A. namibiensis sp. n. are explained under that species. The male genitalia are characterized by the sacculus merged with the medial teeth on the inner margin of the valva in combination with the narrow saccus. The female genitalia differ from other Aphanostola species by the shape of the sub-ostial sclerite, the large globular corpus bursae and the brush-formed signum.
Adult (Figs
Variation. Ground colour of head, thorax and forewing varies from white to light grey, paired black spot on ¾ of dorsal margin expressed in some specimens, medially prolonged spot sometimes divided into two smaller dots. Hindwings in male with light brown scales along margins, particularly on base near dorsal margin.
Male genitalia (Fig.
Female genitalia (Figs
Named after the brown spot in the middle of the forewing.
Namibia, Botswana, South Africa.
The host plant is unknown. The adults were collected in January and March.
Holotype ♂, [South Africa] RSA, Mpumalanga, Hongonyi Lodge, S24°27,17’, E31°4,56’, 30.iv–1.v.2010, LF (Mey & Kühne) (
The new species can reliably be separated from A. antennata sp. n. , A. longicornuta sp. n., and A. alternella sp. n. by the genitalia. The male genitalia are well recognizable by the large and broad sacculus. The female genitalia are characterized by the unmodified sclerite VIII in combination with the funnel-shaped antrum and the small corpus bursae.
Adult (Figs
Male genitalia (Fig.
Male genitalia of Aphanostola spp. 53. A. joannoui sp. n., HT, RSA, Hongonyi Lodge (gen. slide 208/12); 54. A. namibiensis sp. n., Namibia, Brandberg (gen. slide 107/05); 55. A. brandbergensis sp. n., Namibia, Brandberg (gen. slide 103/05); 56. A. aarviki sp. n., HT, Tanzania, Morogoro Town (gen. slide 2380); 57. A. africanella sp. n., HT, Namibia, Omatjete Farm (gen. slide 553/14); 58. A. africanella sp. n., Namibia, Okahanja (gen. slide 198/12).
Female genitalia (Figs
Variation. The antrum is variable in width.
Named in memory of the lepidopterist John Joannou (1949-2013), who participated in the collecting campaign around Hongonyi Lodge with the second author in 2010.
South Africa.
The host plant is unknown. The adults were collected from late March to mid-May.
Genus 1, sp. 3. –
Holotype ♂, Namibia, Brandberg, Wasserfallfläche, 18.iii.2002, LF, 1940 m (gen. slide 107/05, O. Bidzilya) (
The new species resembles externally A. centripunctella sp. n., but differs by the narrower forewing and the smaller, rounded black spot in the middle. The male genitalia are well recognizable by the shape of the sacculus, deep and comparatively broad medial emargination of the posterior margin of the vinculum, the short saccus and the comparatively long uncus. The female genitalia are characterized by distinctly sclerotized patches on segment VIII, short, digitate sub-ostial sclerites, long ductus bursae and the presence of a belt of spikes on the wall of the corpus bursae.
Adult (Figs
Male genitalia (Fig.
Female genitalia (Fig.
The species is named after the country of its occurrence.
Namibia.
The host plant is unknown. The adults were observed in late August, January and March up to 1900 m elevation.
Genus 1, sp. 4. –
Holotype ♀, Namibia, Brandberg, Mason Shelter, 6.iii.2002, 1740 m (Mey) (gen. slide 74/05, O. Bidzilya) (
The new species can easily be recognized by the cream forewing with black dots and black irroration along costal margin and by its comparatively small size. The male genitalia are well defined by the broad valva, the very short saccus, the shape of valva and other details. The female genitalia are characterized by long apophyses anteriores, prolonged corpus bursae and unmodified sternite VIII.
Adult (Fig.
Male genitalia (Fig.
Female genitalia (Fig.
The specific name is derived from the Brandberg, the type locality of the new species.
Namibia.
The host plant is unknown. Adults were collected in December and in February up to 1740 m elevation.
Holotype, ♂, Tanzania, Morogoro, Morogoro Town, 11.iv.1992 (Aarvik) (gen. slide 2380, O. Bidzilya) (MNHO).
The new species remotely resembles externally A. morogorensis sp. n., but is smaller, the forewings are broader and the black spot on ¾ of dorsum is indistinct. The male genitalia somewhat resemble those of A. brandbergensis sp. n., but differ in the short, rounded uncus, longer saccus, slenderer gnathos and the phallus without apical tooth.
Adult (Fig.
Male genitalia (Fig.
Female. Unknown.
The species name is dedicated to Leif Aarvik (Natural History Museum, Oslo), the collector of the species.
Tanzania.
The host plant is unknown. The holotype was collected in mid-April.
Aphanostola sp. 2 –
Holotype ♂, Namibia, Kombat, Omatjete Farm, 27.viii.2012, Turm (Mey) (gen. slide 553/14, O. Bidzilya) (
The new species is externally similar to A. rooiklipella sp. n. and A. melliferae sp. n. but differs in genitalia. The male genitalia are well defined by the phallus bearing seven to eight large cornuti in combination with a long saccus and other details. The female genitalia remotely resemble those of A. morogorensis sp. n., but differ in having a distinctly longer antrum and a narrow, rounded signum.
Adult (Figs
Variation. Black pattern along margins of forewing varies from grey to nearly black.
Male genitalia (Figs
Female genitalia (Figs
The name refers to the obviously wide distribution of the species in Africa.
Namibia, Kenya.
The larva feeds on Acacia mellifera (M. Vahl) Benth. (Fabaceae) in Kenya (
Holotype ♂, [South Africa] RSA, Natal, Mkuzi, [15’sq NW cnr, 27 30’S, 32 05’E], 23–26. Apr. 1982 (Scoble, Laurenson & Kroon) (gen. slide 48/15, O. Bidzilya) (
As far as we can judge from the single male, the new species is most similar to A. kruegeri sp. n. in having brown forewings, but differs in exhibiting a poorly expressed irroration. The male genitalia are well defined by the very deep medial emargination of the posterior margin of the vinculum, a short hump-shaped sacculus and by the absence of the vincular projections.
Adult (Fig.
Male genitalia (Fig.
Male genitalia of Aphanostola spp. 59. A. emarginata sp. n., HT, RSA, Mkuzi (gen. slide 48/15); 60. A. melliferae sp. n., Kenya, L. Bogoria (gen. slode 1549); 61. A. melliferae sp. n., Namibia, Sandveld (gen. slide 457/07); 62. A. maxima sp. n., HT, Ethiopia, Tana-See (gen. slide 427/07); 63. A. longicornuta sp. n., Namibia, Etosha (gen. slide 503/14); 64. A. atripalpis, India, Pusa, PT (gen. slide 411/14).
Female. Unknown.
Derived from “emarginatus” (Latin), excised, referring to the excised vinculum in the male genitalia.
South Africa.
The host plant is unknown. The holotype was collected in late April.
Aphanostola sp. 4 –
Holotype ♀, Kenya: Rift Valley, Lake Bogoria, 1000 m, 0°15’N, 36°05’E, l. Acacia mellifera, em. 30.viii.2007 (Agassiz) (gen. slide 142/15, O. Bidzilya) (coll. Agassiz). Paratypes: 1♂, 2♀, same data as holotype (gen. slide 1549♂, 1550♀, O. Bidzilya); 1♂, KENYA: Rift Valley, Lake Bogoria, 1000 m, 0°21’N, 36°04’E, l. Acacia mellifera, em. 6.xi.2007 (Agassiz); 1♀, KENYA: Rift Valley, Lake Bogoria, 1000 m, 0°21’N, 36°04’E, l. Acacia mellifera, em. 26.viii.2007 (Agassiz); 1♂, 1♀, KENYA: Rift Valley, Lake Bogoria, 1000 m, 0°15’N, 36°7’E, l. on Acacia mellifera, em. 23.xi, 2.xii.2005 (Agassiz) (gen. slide 143/15♂, O. Bidzilya); 1♂, KENYA: Rift Valley, Lake Bogoria, 1000 m, 0°21’N, 36°4’E, l. Acacia mellifera, em. 23.xi.2005 (Agassiz) (all coll. Agassiz); 2♂, 1♀, Namibia, Sandveld, 60 km N Gobabis, 22.–26.i.2007, LF (Mey & Ebert) (gen. slide 457/07♂, O. Bidzilya); 1 ♂, Namibia, Omatako Ranch, LF, 22-23.iii.2003 (Mey) (gen. slide 67/15, O. Bidzilya) (all
The new species can reliably be separated from A. rooiklipella sp. n., and A. africanella sp. n. by the genitalia. A. antennata sp. n. is very similar to above mentioned species, but differs in broader forewing. A. pentastigma is usually larger that A. melliferae sp. n. the forewing are narrower with black spot at base of costal margin. The male genitalia are well recognizable by very short, weakly sclerotized distal portion of valva, stout broadly rounded sacculus and the shape of the phallus. The female genitalia are defined by a characteristically shaped antrum and sub-ostial sclerites as well as by a strongly sclerotized entrance to the corpus bursae which is unique for Aphanostola.
Adult (Figs
Male genitalia (Figs
Female genitalia (Fig.
The species is named after the name of its host plant, Acacia mellifera.
Kenya, Namibia.
Larvae feed on Acacia mellifera in Kenya (
Holotype ♂, [Ethiopia], Äthiopien, 11.-16.i.1996, Tana-See, Bahir-Dar, 1600 m (Mey & Ebert) (gen. slide 427/07, O. Bidzilya) (
A. maxima sp. n. is the largest species of the genus. Besides the big size it is recognizable by comparatively narrow, light brown, uniformly coloured forewing with distinct brown dots in the cell. The male genitalia can be distinguished by broad trapezoidal tegumen, sub-rectangular sacculus, and elongated vinculum.
Adult (Figs
Male genitalia (Fig.
Female. Unknown.
Derived from “maximus” (Latin), the largest, referring to the large size of the species.
Ethiopia.
The type series was collected in mid-January at 1600 m elevation.
Holotype ♀, Namibia, E. Etosha, Farm Sachsenheim, 29.-30.viii.2012, LF (Mey) (
The new species can be separated from the similar A. joannoui sp. n., A. antennata sp. n., and A. alternella sp. n. only by examining the genitalia. The male genitalia can easily be recognized by the presence of a very large, lateral, vincular projection, a long and narrow saccus as well as an extremely long phallus with one large cornutus. The female genitalia are defined by a wrinkled antrum, a narrow, serrated signum, the coiled corpus bursae and by the other details.
Adult (Figs
Variation. The black markings can be reduced so that the forewing looks uniformly grey in some specimens.
Male genitalia (Fig.
Female genitalia (Fig.
Derived from “longus” and “cornutus” (Latin), long resp. cornutus, referring to the unusual long cornutus of the phallus
Namibia, Kenya.
The host plant is unknown. The adults have been collected in late August-early September in Namibia and in mid-April, early July in Kenya.
Aphanostola atripalpis Meyrick, 1931 – Exotic Microlepidoptera 4: 57.
Lectotype: ♂, India, Pusa, Bihar. R. bred. .6.29, reared from Acacia catechu, Rungi (slide No. 8328) (BMNH).
1 ♂, 6.vi.1929, Pupa on leaves of Acacia cati[sic!]chu, Pusa, Rangi Coll., 5699, Cotype, Aphanostola atripalpis, M., Meyrick det. 1980, Presented by R.L.E. Ford, B.M. 1949-487 (gen. slide 411/14, O. Bidzilya) (BMNH).
As far as we can judge from rather limited material, A. atripalpis differs from the other species by the uniformly greyish-brown forewings and the whitish head. The male genitalia have a rounded uncus covered with very short setae.
Adult (Fig.
Male genitalia (Fig.
Female. Not examined.
India.
Larva feeds on Acacia [Senegalia?] catechu (L.f) P.J.H. Hurter & Mabb. (Fabaceae). Adults emerged in June.
A. atripalpis was described from two males collected in Bihar, Pusa (India). The adult moth and the venation, and the male genitalia in lateral position, were illustrated by
Female genitalia of Aphanostola spp. 74. A. centripunctella sp. n., Namibia, Katima Mulilo (gen. slide 508/14); 74a. Signum (gen. slide 76/05); 75. A. joannoui sp. n., RSA, Hongonyi Lodge (gen. slide 81/12); 75a. Subostial sclerite (gen. slide 209/12); 76. A. namibiensis sp. n., Namibia, Etosha (gen. slide 534/14).
Female genitalia of Aphanostola spp. 77. A. brandbergensis sp. n., HT, Namibia, Brandberg (gen. slide 74/05); 78. A. africanella sp. n., Namibia, Fort Sesfontein (gen. slide 489/14); 79. A. africanella sp. n., Kenya, L. Baringo (gen. slide 1363); 79a. Signum (enlarge) (gen. slide 1370).
We are thankful to Leif Aarvik (
The first author expresses his gratitude to Jurate De Prins for her assistance during his work in the collection of BMNH, in particular for providing photo equipment.
The visits of the first author to
We are thankful to the editor of DEZ and two reviewers, who made constructive suggestions to improve the manuscript. Authors are acknowledged the