Spalangia gemina Bouček, 1963
publication ID |
https://doi.org/ 10.11646/zootaxa.4858.1.3 |
publication LSID |
lsid:zoobank.org:pub:A2E85BBC-F1DA-41FE-B2A2-AA086F39186E |
DOI |
https://doi.org/10.5281/zenodo.4411537 |
persistent identifier |
https://treatment.plazi.org/id/1137956E-FFB6-FFFF-FF27-B3A7FAF4FAA5 |
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Plazi |
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Spalangia gemina Bouček, 1963 |
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Spalangia gemina Bouček, 1963 View in CoL
( Figs 10, 13 View FIGURES 9–17 )
Diagnosis. Head with dense circular setiferous punctures; gena with malar space distinctly shorter than eye height and malar sulcus absent; pronotal collar coarsely reticulate-rugose, except for a nearly triangular area close to the crenulate cross-line posteriorly; mesoscutal median lobe with median longitudinal carina separating two groups of irregular foveae posteriorly ( Bouček 1963; Gibson 2009).
Taxonomy. See S. endius .
Biology. Most of the host records of this parasitoid are from tephritids. There are also reports of this species as hyperparasitoid, using tachinids ( Diptera ) as primary hosts, all in Lepidoptera . Other hosts include Musca domestica L. and species of Drosophila . Spalangia gemina has apparently a narrower host range than S. endius , and experiments showed that some hosts, including Drosophila virillis Sturtevant and A. ludens , are not parasitized by S. gemina ( Sivinski et al. 1998) . Tephritid hosts in Brazil include A. obliqua ( Uchôa et al. 2003) and Ce. capitata ( Silva et al. 2020) .
Biological control. See S. endius .
Distribution. Mainly tropical, but reaching temperate zones of the New and Old World, and Australasia.
Distribution in Brazil (associated with Tephritidae ). MS ( Uchôa et al. 2003) and RN ( Silva et al. 2020).
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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