TRIBE CATOCALINI
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This tribe, as circumscribed for this work (a broader concept is adopted by Fibiger (2003), who treated the grouping here as a subtribe), was investigated in detail by Mitter & Silverfine (1988); it includes in synonymy the Audeinae of Wiltshire (1990), a nomen nudum according to Speidel & Naumann (2005).

The definitive features in the female genitalia are: elongated, narrow, tapering ovipositor lobes with a longitudinal band of sclerotisation extending through them from the apophyses (but see also the Catephiini on p. 84, Ericeia Walker on p. 116, Dinumma Walker on p. 242, Hamodes Guenée on p. 267 and Chilkasa Swinhoe on p. 291); an ostium set well anterior at the end of a deep cleft with the seventh sternite. The posterior margin of the sternite is represented by lobes at the end of the cleft, but it is not clear that these are homologous with the bilobed condition of the antevaginal plate seen in other tribes such as the Ophiusini, given that it is entire in some genera, covering the ostium. The cleft seventh sternite is seen also in the putative sister-genus Metatacha Hampson.

The male genitalia were found by Mitter & Silverfine to be difficult to interpret. The features are generally as in the core Catocalinae as discussed on p. 17, but the valves distally are divided into a strongly sclerotised costa and a membranous to corematous distal part suspended from the costa. There is usually a single, finger-like process from the sclerotised sacculus; its relationship to features in a similar position in, say, the Ophiusini (p. 40) is unclear. The valves often show bilateral asymmetry. The juxta is of the inverted ‘Y’ type, and the structures of the uncus, scaphium and aedeagus are consistent with the general condition of the core catocalines.

However, unlike most core catocalines, the male eighth segment shows vestiges of the framed corematous condition in many taxa (e.g. Fig 4) both in the sternite and the tergite, and in some taxa its development is more obvious (Figs 25 and 26 in Mitter & Silverfine (1988)). If the interpretation of lack of modification of this segment as a synapomorphy for a core catocaline group is valid, then the group of genera including
Catocala Schrank might be placed relatively basally within this core group, perhaps also supported by the somewhat different structure of the ostium and seventh sternite in the female. Given these uncertainties, it would be preferable to retain this narrow concept of the Catocalini separate from other core catocaline tribes for the time being.




Larval and pupal features (e.g. a bloom) support a general association of the group with other core catocalines as discussed on p. 22 and p. 24, though reduction of the prolegs is only slight.

Mitter & Silverfine (1988) presented a phylogeny for the group that separated
Catocala and Ulotrichopus Wallengren from a predominantly African clade that included Audea Walker, Crypsotidia Rothschild and Hypotacha Hampson. Within the Catocala clade, Ulotrichopus species showed monophyly but were nested within Catocala. Recognition of Ulotrichopus as a good genus (e.g. as in Kobes (1985), Poole (1989) and Fibiger (2003)) would render Catocala paraphyletic in this system, therefore Ulotrichopus is included as a synonym of Catocala, an arrangement also adopted by Fu & Tzoo (2002).

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