Lobogonodes Bastelberger, 1909
publication ID |
https://doi.org/ 10.11646/zootaxa.4433.3.2 |
publication LSID |
lsid:zoobank.org:pub:AC05E2BD-6BB6-409E-B752-0DE44668A76C |
DOI |
https://doi.org/10.5281/zenodo.5998459 |
persistent identifier |
https://treatment.plazi.org/id/7B49EE19-E077-FFF7-72E7-21DEA1B9FE75 |
treatment provided by |
Plazi |
scientific name |
Lobogonodes Bastelberger, 1909 |
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Genus Lobogonodes Bastelberger, 1909 View in CoL
( Figs 1 – 43 View FIGURES 1–15 View FIGURES 16–23 View FIGURES 24–31 View FIGURES 32–37 View FIGURES 38–43 )
Lobogonodes Bastelberger, 1909 View in CoL , Deutsche entomologische Zeitschrift Iris 22: 168. Type species Hypenorhynchus View in CoL ? permarmorata Bastelberger, 1909 View in CoL , Entomologische Zeitschrift (Frankfurt a. M.) 23(7): 34, by original designation.
Microlygris Prout, 1914 View in CoL , Gross-Schmett. 4: 207. Type species: Cidaria multistriata Butler, 1889 , Illustrations of typical Specimens of Lepidoptera Heterocera View in CoL in the Collection of the British Museum 7: 24, 119, pl. 137, fig. 21, by original designation.
Taxonomic notes and diagnosis. The wing patterns of Lobogonodes and related genera in the Eulithis group (tribe Cidariini ) are discussed in detail by Choi (2001). Most species of Lobogonodes have multiple parallel transverse lines on the fore- and hindwing, however, the genotype L. permarmorata ( Figs 1, 2 View FIGURES 1–15 ) and the newly described Taiwanese species L. shiushioui sp. nov. ( Figs 3, 4 View FIGURES 1–15 ) have dentate lines that are particular to the Cidariini .
Prout (1937; 1940) recognized Lobogonodes and Microlygris Prout, 1914 as two groups within Lobogonodes based on the presence of a hair pencil under the male forewing of the latter and the different status of the M1, i.e. more or less stalked with R 2-5 in the former and free in the latter. Choi (2001) indicated that the hair pencil is useful for species diagnosis within the tribe but is an inconsistent character at the generic level; therefore he synonymized the two genera.
It is necessary to revise some character states of the male genitalia in Lobogonodes in the recent study of Choi (2001). Rather than a membranous subscaphium lacking a sclerotized band, a sclerotized band of the subscaphium can be observed in all members of Lobogonodes in the present study ( Figs 16 – 23 View FIGURES 16–23 ). The U-shaped connection of juxta and anellus of L. multistriata claimed as unique in the tribe ( Choi 2001), is now confirmed as present in all the Lobogonodes species examined. The shape of the anellus is variable within the genus. The laterally bilobed anellus of L. multistriata ( Fig. 22 View FIGURES 16–23 ) ( Choi 2001), is slightly bilobed in the Indian and Nepalese L. porphyriata ( Fig. 23 View FIGURES 16–23 ), whereas the anellus of other congeneric species is simply expanded apically. The absence of a cornutus in Lobogonodes was noted by Choi (2001). In the present study, three distinct types of cornutus can be found in Lobogonodes : absent in L. permarmorata ( Fig. 24 View FIGURES 24–31 ); slightly sclerotized at distal part of vesica in three species previously placed in Microlygris , i.e. L. complicata , L. porphyriata and L. multistriata , as well L. dactylotypa stat.rev. ( Figs 28–31 View FIGURES 24–31 ); and as a long, band-shaped sclerite in L. taiwana , L. erectaria and L. shiushioui sp. nov. ( Figs 25–27 View FIGURES 24–31 ). The latter character state is similar to that seen in the Palearctic Lampropteryx suffumata (Denis & Schiffermuller, 1775) . These three types of cornutus can be useful for grouping species within Lobogonodes .
In the female genitalia, the signum status was described as one single dot without circular sclerotization in L. multistriata by Choi (2001), now shown to also occur in L. permarmorata , L. erectaria , L. taiwana ( Figs 32–34 View FIGURES 32–37 ) of group Lobogonodes sensu Prout (1940) . The signum of L. complicata and L. dactylotypa stat. rev. presents as a flattened wide plate ( Fig. 35, 36 View FIGURES 32–37 ) and of multistriata as a conical horn ( Fig. 37 View FIGURES 32–37 ), and these three species belong to the group Microlygris sensu Prout (1937 ; 1940). The length of the ductus bursae compared to the 7th abdominal segment was used by Choi (2001) for separating some species. Similar to L. multistriata ( Choi 2001) , the species L. erectaria , L. taiwana , L. complicata , have the length of ductus bursae nearly as long as the 7th segment. However, the genotype species L. permarmorata has an extremely long ductus, nearly three times longer than the 7th segment ( Fig. 32 View FIGURES 32–37 ). Choi (2001) noted the very long ductus bursae in Lampropteryx suffumata as twice as long as the 7th segment.
Distribution and bionomics. From the Himalayan region to East Asia (E. China, S. Primorye, Korea, Japan and Taiwan). Taiwan is the most speciose region having 4 species (2 endemic). The adults infrequently occur from early spring to summer.
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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Lobogonodes Bastelberger, 1909
Wu, Shipher & Chang, Wei-Chun 2018 |
Microlygris
Prout 1914 |
Lobogonodes
Bastelberger 1909 |
permarmorata Bastelberger, 1909
: Bastelberger 1909 |
Hypenorhynchus
Hampson 1895 |
Cidaria multistriata
Butler 1889 |