Metapelma Westwood, 1868
publication ID |
https://dx.doi.org/10.3897/zookeys.926.48688 |
publication LSID |
lsid:zoobank.org:pub:5A4CA4BA-59C1-4114-9370-F15834AB6476 |
persistent identifier |
https://treatment.plazi.org/id/4F9BEE90-F21F-534F-9321-ED901C6DBB50 |
treatment provided by |
ZooKeys by Pensoft (2020-04-14 15:43:52, last updated 2022-11-11 12:11:56) |
scientific name |
Metapelma Westwood, 1868 |
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Main history of Oriental and Palaearctic species.
Westwood (1835) established Metapelma with M. spectabile Westwood as the type species from North America. Förster (1856) subsequently described Halidea based on H. nobilis from Germany, but Ashmead (1896) synonymized Halidea under Metapelma (see Gibson 1989 for further remarks on generic synonymy).
Until now, 15 valid extant species of Metapelma from the Oriental and Palaearctic regions are known, namely M. albisquamulatum Enderlein from the Philippines, M. beijingense from China, M. compressipes Cameron from Malaysia, M. gloriosum Westwood from the Philippines, M. kokkaricum Narendranand & Abhilash from India, M. mesandamna Mani & Kaul from India, M. nobilis ( Förster) from Germany, M. obscuratum Westwood from India, M. pacificum Nikolskaya from Russia, M. periyaricum Narendranand & Mohana from India, M. rufimanum Westwood from Malaysia (Sarawak), M. strychnocola Mani & Kaul from India, M. taprobanae Westwood from Sri Lanka, M. tenuicrus Gahan from the Philippines, and M. zhangi Yang from China.
Recognition.
Metapelma is one of four extant genera described for Neanastatinae ( Eupelmidae ). The genus is differentiated from the other three genera using the keys by Gibson (1995, 2009), but indivduals can be recognized uniquely by the following combination of characters: head lenticular with short scrobe above each torulus but scrobes not united into a common scrobal depression (Fig. 3C View Figure 3 ); antenna 13-segmented with flagellum composed of longer than wide anellus, seven funicular segments, and 3-segmented clava (Fig. 3D View Figure 3 ); scutellum entire, not divided longitudinally (Fig. 3E View Figure 3 ); mesopleuron with upper and lower mesepimeron differentiated posteriorly behind acropleuron (Fig. 4A, B View Figure 4 ); hind tibia usually conspicuously compressed and widened apically (Fig. 3A View Figure 3 ).
Ashmead, WH, 1896. On the genera of Eupelminae. Proceedings of the Entomological Society of Washington 4: 4 - 20
Foerster, A, 1856. Hymenopterologische Studien. II. Heft. Chalcidiae und Proctotrupii, Aachen
Gibson, GAP, 1989. Phylogeny and classification of Eupelmidae, with revision of the world genera of Calosotinae and Metapelmatinae (Hymenoptera: Chalcidoidea). Memoirs of the Entomological Society of Canada 149: 1 - 121, DOI: https://doi.org/10.4039/entm121149fv
Gibson, GAP, 1995. Parasitic wasps of the subfamily Eupelminae (Hymenoptera: Chalcidoidea: Eupelmidae). Memoirs on Entomology International 5: 1-5 + 1-421.
Gibson, GAP, 2009. Description of three new genera and four new species of Neanastatinae (Hymenoptera, Eupelmidae) from Baltic amber, with discussion of their relationships to extant taxa. In: Johnson, N, Ed., Advances in the systematics of Hymenoptera. Festschrift in honour of Lubomir Masner. ZooKeys 20: 175 - 214, DOI: https://doi.org/10.3897/zookeys.20.161
Westwood, JO, 1835. Characters of new genera and species of hymenopterous insects. Proceedings of the Zoological Society of London 3: 51-54, 68-72.
Figure 3. Metapelma beijingense Yang, ♀, China, Guizhou. A Habitus, dorsal aspect B head, dorsal aspect C head, anterior aspect D antennae, lateral aspect E mesosoma, dorsal aspect.
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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