Copturomimus Heller, 1895: 63

Anzaldo, Salvatore S., 2017, Review of the genera of Conoderinae (Coleoptera, Curculionidae) from North America, Central America, and the Caribbean, ZooKeys 683, pp. 51-138 : 69-71

publication ID

https://dx.doi.org/10.3897/zookeys.683.12080

publication LSID

lsid:zoobank.org:pub:D7FD86CA-6374-480C-821B-A10C26CDDF32

persistent identifier

https://treatment.plazi.org/id/529F9C26-0BBA-D389-923D-DD1F23B8F72C

treatment provided by

ZooKeys by Pensoft

scientific name

Copturomimus Heller, 1895: 63
status

 

Copturomimus Heller, 1895: 63 Figs 66 View Figures 55–66 , 74 View Figures 71–74

Type species.

Copturomimus cinereus Heller, 1895 [by present designation].

Gender.

Masculine.

Diagnosis.

Copturomimus is similar to the large genus Macrocopturus with the elongate second funicular article, unmodified mesoventrite, and carinate and ventrally toothed hind femora, and can only be distinguished externally from that genus by the obliquely striolate area dorsally on the profemora (Fig. 66 View Figures 55–66 ). The other genus with a striolate patch on the profemora, Copturomorpha , tends to have a striolate patch that is less obvious, being more finely striolate and more often concealed by scales; that genus otherwise is more similar to Eulechriops .

Notes.

The function of the striolate profemora is unknown - the first conoderine species described with it, Copturomorpha musica ( Kirsch 1875b), was named, as the specific epithet suggests, for its hypothesized stridulatory function ( Kirsch 1875b: 248). The function of the patch was instead suggested to be for antennal grooming purposes ( Champion 1906b: 60) due to the lack of an obvious corresponding file structure required for stridulation and the position of the leg relative to the antennal club - observation of Copturomimus caeruleotinctus Champion, 1906 [SSAC0001059] revealed the use of the setal comb at the protibial apex (and not the striolate femoral patch) for antennal cleaning purposes.

Keys .

Champion 1906b: 60 (for Central America), Muñiz 1965: 5 (for three species on avocado, key modified from Muñiz and Barrera 1958: 2).

Phylogenetic relationships.

Heller (1895: 63) originally implied a relationship with his South American genus Copturosomus Heller, 1895, which is also difficult to distinguish from Macrocopturus . The relationship of both genera with Macrocopturus requires much more study to identify natural groupings of species. Whether the striolate femoral patch identifies a natural group is unknown but unlikely ( Hespenheide 2009: 337). See also entry on Macrocopturus for discussion of the relationships of that hypothesized complex of genera.

Host association

. Copturomimus perseae (Guenther, 1935) and two other South American species are wood-boring on avocado ( Lauraceae : Persea Mill.) (Hustache in Mariño M. 1947, Kissinger 1957, Muñiz 1965). Associations of other Central American species are unknown.

Described species.

Twelve species are known from the focal region (one species described by Hespenheide 2009) and five additional species are known from South America ( Wibmer and O’Brien 1986: 271; Muñiz 1965 transferred one species from Copturus ).

Range.

Mexico, Guatemala, Honduras, Costa Rica, Panama; South America.

Kingdom

Animalia

Phylum

Arthropoda

Class

Insecta

Order

Coleoptera

Family

Curculionidae