Vavizola, Prozorov & Prozorova & Nedoshivina & Yakovlev & Volkova & Saldaitis & Revay & Müller, 2023
publication ID |
https://doi.org/ 10.37828/em.2023.62.8 |
publication LSID |
urn:lsid:zoobank.org:pub:0B251B97-8DD3-4C72-90F1-FDCAA28DED2D |
DOI |
https://doi.org/10.5281/zenodo.8059223 |
persistent identifier |
https://treatment.plazi.org/id/06558427-344F-44B3-A355-3686BD8978B9 |
taxon LSID |
lsid:zoobank.org:act:06558427-344F-44B3-A355-3686BD8978B9 |
treatment provided by |
Felipe |
scientific name |
Vavizola |
status |
gen. nov. |
Vavizola gen. n.
https://zoobank.org/ urn:lsid:zoobank.org:act:06558427-344F-44B3-A355-3686BD8978B9
( Figs 1–10 View Figures 1–4 View Figures 5–20 , 21–22 View Figures 21–27 , 28 View Figures 28–33 , 34 View Figure 34 )
Diagnosis. The detailed description of morphology is provided for the new species below, since the genus is monotypic. Habitus of Vavizola gen. n. reminds us of some other members of “ Pachypasa sensu lato ” revised by Zolotuhin & Gurkovich (2009): 1) Seydelora Zolotuhin & Gurkovich, 2009 ; 2) Gufria Zolotuhin & Gurkovich, 2009 ; 3) Lasiocesa Koçak, 2013 ; 4) Braura Walker, 1865 ; and 5) Eutricha Hübner, 1814 . Adults of all genera have a diagonal wing pattern, cubile in male genitalia and a corresponding antevaginal plate in female genitalia.
1) Seydelora includes only Seydelora semna ( Hering, 1941) from DRC. It has very dark forewings with dark brown medial, postmedial and external fields and a complex speckled white or yellow and brown external fascia; hindwings have a well pronounced dark external field ( Figs 13–14 View Figures 5–20 ). Male adults of Vavizola gen. n. are overall lighter, their forewings are more elongated, medial field is more elongated towards the wing apex, postmedial fascia is developed, the medial white triangle on thorax is absent (compare Figs 5–6, 8–9 and 13 View Figures 5–20 ); male genitalia of Vavizola gen. n. differ by shorter cucullus and sacculus, and smaller apodema of cubile (compare Figs 21–22 and 25 View Figures 21–27 ). Female adults of Vavizola gen. n. are overall lighter, their forewings are more elongated, forewing pattern is shifted more towards the wing apex, postmedial and external lines are doubled, medial pale speckled thoracic spot is absent (compare Figs 7, 10 and 14 View Figures 5–20 ); female genitalia of Vavizola gen. n. differ in the shape of sterigma and presence of cup-like antrum (compare Figs 28 and 29 View Figures 28–33 ).
2) Zolotuhin & Gurkovich (2009) considered the genus Gufria to be monotypic with the only member Gufria limosa de Villiers, 1827 distributed from Southern Europe to North Africa. We suppose that European and African populations will show a genetic divergence, sufficient to be considered a separate species, similar to experiences with Lemonia philopalus ( Donzel, 1842) (see Prozorov et al., 2022b). Here, for comparison, we take adults of G. limosa from Tunisia and Morocco and call them Gufria limosa powelli ( Oberthür, 1916) – the earliest taxon from North Africa. Adults are colored in combinations of grey, creamy and brown; medial field on forewing stretches until the wing apex, postmedial field is paler than the others ( Figs 17–18 View Figures 5–20 ). Male adults of Vavizola gen. n. have more elongated forewings with medial field not reaching the wing apex, and postmedial lines (compare Figs 5–6, 8–9 and 17 View Figures 5–20 ); male genitalia of Vavizola gen. n. differ with shorter cucullus and sacculus, shorter distal outgrowths and lack of lateral dents (compare Figs 21–22 and 23 View Figures 21–27 ). Female adults of Vavizola gen. n. have more elongated forewings, their forewing pattern consists of more elements and both wings have dark external field (compare Figs 7, 10 and 18 View Figures 5–20 ); antevaginal plate in female genitalia of Vavizola gen. n. is better developed and antrum is wider (compare Figs 28 and 31 View Figures 28–33 ).
3) Lasiocesa includes 4 species. Here, for comparison, we take adults ( Figs 15–16 View Figures 5–20 ) and male genitalia ( Fig. 26 View Figures 21–27 ) of the type-species Lasiocesa fulgurata ( Aurivillius, 1909) and female genitalia ( Fig. 32 View Figures 28–33 ) of Lasiocesa lanceolata ( Hering, 1932) due to only one known bad quality slide of female genitalia of L. fulgurata , all from DRC. Adults are colored in combinations of brown and creamy, forewing has full set of fields and fasciae, while hindwing may be completely brown or creamy with brown external field. Wing pattern of both genera is very similar, however, Vavizola gen. n. is much paler and duller, have narrower postmedial field (compare Figs 5–10 and 15–16 View Figures 5–20 ). Male genitalia of Vavizola gen. n. differ with shorter cucullus, larger sacculus, and lack medial ridges on processes of cubile (compare Figs 21–22 and 26 View Figures 21–27 ). Female genitalia of Vavizola gen. n. differ with larger antevaginal plate and presence of cup-like antrum (compare Figs 28 and 32 View Figures 28–33 ).
4) Braura includes 9 species. For comparison, we take the type-species Braura ligniclusa ( Walker, 1865) from RSA. Adults have dark brown forewings with occasionally paler medial field, hind wings dark brown or creamy with darker external field. Male adults of Vavizola gen. n. are overall lighter, but head and thorax cranially are not contrasting (compare Figs 5–6, 8–9 and 11 View Figures 5–20 ); male genitalia of Vavizola gen. n. differ with smaller cucullus and basally larger sacculus, smaller caudal processes of cubile (compare Figs 21–22 and 24 View Figures 21–27 ). Female adults of Vavizola gen. n. are overall lighter, but head, thorax cranially, and forewing medial field are not contrasting (compare Figs 7, 10 and 12 View Figures 5–20 ); female genitalia of Vavizola gen. n. differ in better developed antevaginal plate and presence of cup-like antrum (compare Figs 28 and 30 View Figures 28–33 ).
5) Eutricha includes 5 species ranging in coloration from creamy to dark brown. Here, for comparison, we use Eutricha capensis ( Linnaeus, 1767) from RSA, the type-species of the genus. Adults have well pronounced contrasting postmedial and external fasciae. Male adults of Vavizola gen. n. are overall lighter, their forewings are more elongated, medial field is more elongated towards the wing apex (compare Figs 5–6, 8–9 and 19 View Figures 5–20 ); male genitalia of Vavizola gen. n. differ with smaller cucullus and sacculus, smaller apical dent of aedeagus (compare Figs 21–22 and 27 View Figures 21–27 ). Female adults of Vavizola gen. n. are overall paler and duller with contrasting external field (compare Figs 7, 10 and 20 View Figures 5–20 ); female genitalia of Vavizola gen. n. differ in shape of sterigma (compare Figs 28 and 33 View Figures 28–33 ).
DNA comparison ( Fig. 34 View Figure 34 ). Two specimens of Vavizola hela sp. n. were sequenced: the holotype male from Tanzania ( Fig. 5 View Figures 5–20 ) and the paratype female from Kenya ( Fig. 10 View Figures 5–20 ). The two have a 0.8% p -distance which is a little higher than we expected for specimens of a single species collected so closely together. It may be explained by the1200 meters difference in the altitude between collecting localities of the two. The new genus is compared with 18 sequences belonging to 12 biological index numbers (BINs) and 9 genera from the “ Pachypasa sensu lato ” group, missing Seydelora ; Pachyna Weymer, 1892 ; Beriola Zolotuhin & Gurkovich, 2009 ; Euphorea Zolotuhin & Gurkovich, 2009 ; and Sophyrita Zolotuhin & Gurkovich, 2009 (see Table 1 View Table 1 ). We will only compare the new genus with the others without investigation of their internal concerns such as potential polyphyly of Pachytrina Zolotuhin & Gurkovich, 2009 or polytypy of Muzunguja which follow from the tree and p -distances. These differences require a detailed investigation.
We can see that intergeneric p -distance lays between 4.7 and 12% ( Fig. 34 View Figure 34 ), where the lowest is between Pallastica Zolotuhin & Gurkovich, 2009 and Cleopatrina Zolotuhin & Gurkovich, 2009 , and the highest is between Muzunguja and Lasiocesa . The nearest neighbor of Vavizola gen. n. (BOLD:AAV0301) found on BOLD is Eutricha morosa ( Walker, 1865) from Malawi (BOLD:ABZ6351) at 5.92%. We selected two other Eutricha species which are not much farther: 6.4 and 7.4%. Other sequences, except Pachytrina sp. at 6.1% ( Fig. 34 View Figure 34 , 10 View Figures 5–20 ), are farther than any Eutricha .
Etymology. Name of the new genus is devoted to Prof. Dr. Vadim Viktorovich Zolotuhin (1967–2021), Russian entomologist specialized on the Old World Lasiocampidae . It is formed by a combination of the first letters of his name by analogy with Tarsozeuzera vavizola Yakovlev, 2006 (Cossidae) .
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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