TRIBE ERCHEIINI
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Ercheia cyllaria Cramer
Noctua cyllaria Cramer, [1779] 1782, Uitlandsche Kapellen, 3: 100.
Achaea cyllota Guenée, 1852, Hist. Nat. Insectes, Spec. gén. Lépid. 7: 248.
Achaea fusifera Walker, 1858, List Specimens lepid. Insects Colln Br. Mus., 14: 1398.
Achaea signivitta Walker, 1858, List Specimens lepid. Insects Colln Br. Mus., 14: 1398.
Achaea polychroma Walker, 1858, List Specimens lepid. Insects Colln Br. Mus., 14: 1400.
Achaea atrivitta Walker, 1864, J. Linn. Soc. (Zool.), 7: 181.
Achaea purpureilinea Walker, 1864, J. Linn. Soc. (Zool.), 7: 181.
Achaea semipallida Walker, 1864, J. Linn. Soc. (Zool.), 7: 181.
Ercheia tenebrosa Moore, 1867, Proc. zool. Soc. Lond., 1867: 66.
Melipotis gundiana Felder, 1874, Reise öst. Fregatte Novara, Lep: pl. 116, f. 10.
Melipotis costipannosa Moore, 1882, Descr. new Indian lepid. Insects Colln W.S. Atkinson: 166.
Ercheia pannosa Moore, 1883, Proc. zool. Soc. Lond., 1883: 24.
Ercheia uniformis Moore, 1883, Proc. zool. Soc. Lond., 1883: 24.
Ercheia anvira Swinhoe, 1918, Ann. Mag. nat. Hist (9) 2: 77, syn. n.
Ercheia cyllaria
Cramer; Holloway, 1976: 30; Kobes, 1985: 36.

Ercheia cyllaria Ercheia cyllaria
Ercheia cyllaria Ercheia cyllaria Ercheia cyllaria


Diagnosis. This is a highly variable species as illustrated (see also Kobes (1985)), but its forms are best distinguished by eliminating the possibility of a specimen being one of the remainder discussed.

Taxonomic note
. The taxon anvira Swinhoe, described from G. Kinabalu, is merely another form of cyllaria.

Geographical range. Indian Subregion, Taiwan, Japan, Indochina, Thailand, Peninsular Malaysia, Sumatra, Borneo, Seram, Kei. Habitat preference. This is a very common species from the lowlands to 2000m and has been recorded as high as 2600m. It is often common in secondary forest and softwood plantations also (Chey, 1994).

Biology. Bell (MS) described the larva. The prolegs on A4 are slightly reduced, those on A3 half-sized. There are small dorsolateral tubercles on A8 and A9 set on slightly swollen transverse ridges. In the penultimate instar, the head is very pale pink, with a soiled appearance and marked in black and brown. The body above is dark chocolate-brown, finely marbled with yellow that also forms indistinct bands subdorsally and on each side of the spiracles. Ventrally there is a jet black central band, flanked by yellow, that expands between the prolegs into patches. The prolegs are pinkish. The anal prolegs bear a black, spectacle-like mark. The final instar has the head light yellow in ground colour, the body similar to before, but with more red ventrally between the anterior two pairs of prolegs. Variants are more variegated with very pale green stippled with dark brown, or light yellowish brown, dotted with chocolate spots and lined with slightly paler bands. Possibly the larva is as variable as the adult.

Pupation is in a cell made from leaves cut to form a sort of triangular tag joined with silk. The surface of the pupa is finely granular, but does not have a powdery bloom.

Host plants recorded (Robinson
et al., 2001) are Asparagus (Asparagaceae), Brassica (Cruciferae), Dalbergia (Leguminosae), Grewia (Tiliaceae) and indeterminate Gramineae. Bell (MS) suggested the diet might be much wider. The adult is noted as a fruit piercer in Thailand (Bänziger, 1982; Kuroko & Lewvanich, 1993).

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