Habrocampulum Gauld, 1976

Shimizu, So, 2016, Recognition of the genus Habrocampulum Gauld, 1976 (Hymenoptera: Ichneumonidae: Anomaloninae) from Japan, with a new combination and a key to the species, Zootaxa 4103 (3), pp. 283-288 : 285

publication ID

https://doi.org/ 10.11646/zootaxa.4103.3.7

publication LSID

lsid:zoobank.org:pub:9087BA69-4DCB-4F61-A938-E0D258BA415E

DOI

https://doi.org/10.5281/zenodo.6067065

persistent identifier

https://treatment.plazi.org/id/03D687D7-FFEF-FFF4-FF24-FF255E37FB9F

treatment provided by

Plazi

scientific name

Habrocampulum Gauld, 1976
status

 

Genus Habrocampulum Gauld, 1976 View in CoL

Habronyx (Habrocampulum) Gauld, 1976: 38 . Type-species: Anomalon biguttatum Gravenhorst, 1829: 642 . Habrocampulum Schnee, 1989: 245 View in CoL . New status, raised to genus from subgenus.

Diagnosis. This genus can be distinguished from other genera of Anomaloninae by the following combination of character states: (1) eyes bare; (2) lower margin of clypeus with a median apical tooth ( Figs 2, 4 View FIGURES 2 – 6 ); (3) frons with a median longitudinal carina ( Figs 2, 3 View FIGURES 2 – 6 ); (4) occipital carina complete ( Figs 3–5 View FIGURES 2 – 6 ); (5) mandible with two distinct teeth ( Fig. 2 View FIGURES 2 – 6 ); (6) upper margin of pronotum with a weak longitudinal impression ( Fig. 5 View FIGURES 2 – 6 ); (7) antero-ventral corner of pronotum with a tooth ( Fig. 5 View FIGURES 2 – 6 ); (8) mesoscutum rounded, and its anterior margin with a weak concavity ( Fig. 5 View FIGURES 2 – 6 ); (9) notauli present ( Fig. 5 View FIGURES 2 – 6 ); (10) epicnemial carina present, its upper end reaching front margin of mesopleuron at the level of lower end of pronotum ( Fig. 5 View FIGURES 2 – 6 ); (11) posterior transverse carina of mesosternum interrupted at the front of mid coxa; (12) scutellum convex ( Fig. 5 View FIGURES 2 – 6 ); (13) postscutellum longer than its width ( Fig. 6 View FIGURES 2 – 6 ); (14) fore wing with CI=0.8–1.1; (15) 2rs-m on fore wing straight; (16) hind wing with Cu1; (17) fore coxa smooth, without carina or its vestige; and (18) mid tibia with two spurs.

Distribution. Nearctic ( Canada and United States of America) and Palaearctic ( Belgium, Czech Republic, Czechoslovakia, Finland, France, Germany, Latvia, Netherlands, Poland, Russia, Spain, Sweden, and United Kingdom) regions ( Yu et al. 2012). New to Japan.

Bionomics. Two noctuid moths ( Agrotis segetum and Panolis flammea ), four geometer moths ( Bupalus piniarius , Caripeta divisata , Macaria granitata , and M. liturata ), and a single lasiocampid moth ( Dendrolimus pini ) have been reported as hosts of H. biguttatum ( Yu et al. 2012) .

Remarks. This genus is closely related to Aphanistes , Barylypa , and Habronyx based on morphological characteristics ( Gauld 1976). Japanese species of Habrocampulum have previously been misidentified as Aphanistes , because they are closely related and have common characteristics (e.g., anterior margin of mesoscutum with concavity and frons with a median longitudinal carina), but Habrocampulum can be distinguished from Aphanistes and the other Japanese genera of Anomaloninae by the following update key.

Kingdom

Animalia

Phylum

Arthropoda

Class

Insecta

Order

Hymenoptera

Family

Ichneumonidae

Loc

Habrocampulum Gauld, 1976

Shimizu, So 2016
2016
Loc

Habronyx (Habrocampulum)

Schnee 1989: 245
Gauld 1976: 38
1976
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