Leptopilina australis (Belizin, 1966)
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publication ID |
https://doi.org/10.3897/jhr.98.165583 |
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publication LSID |
lsid:zoobank.org:pub:E9A78FC5-6B58-4565-86EB-098C72908514 |
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DOI |
https://doi.org/10.5281/zenodo.17435376 |
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persistent identifier |
https://treatment.plazi.org/id/79109910-1D91-5C11-8A05-46BAFB55238D |
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scientific name |
Leptopilina australis (Belizin, 1966) |
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Leptopilina australis (Belizin, 1966)
Rhoptromeris australis Belizin, 1966: 87 .
Diagnosis.
Leptopilina australis is a relatively small species ( 1.3–1.4 mm ♀ body length in a small number of measured females) with somewhat slender appearance and a relatively short antenna (Fig. 2 A View Figure 2 ).
The species is unique in the combination of the mesoscutum having rows of setae mediolaterally (Fig. 11 A View Figure 11 , susceptible to damage), a state shared with L. clavipes (mesoscutum glabrous in other species), and the short metapleural ridge 1 (Fig. 2 D View Figure 2 , see Fig. 9 A View Figure 9 for an overview on the metapleural ridges 1–3). The short ridge is shared with L. fimbriata , but in other species it is either absent ( L. boulardi ) or at least half the length of the metapleuron.
The metapleural ridge 2 is shorter than half the length of the metapleuron, albeit longer than ridge 1 (Fig. 2 D View Figure 2 ). The ridge 2 is equally long in L. boulardi , L. clavipes and L. fimbriata but at least half the length of the metapleuron in the other species.
A setal patch on the base of the hind coxa is present (Fig. 2 D View Figure 2 ), in contrast to L. japonica and L. boulardi , where there are at most a few singular setae that are not arranged in a patch.
Biology.
Habitat. Occurs in parks and forests, mainly in nemoral deciduous forest, with decaying plant material and fungal fruiting bodies. In one study, the species emerged from Drosophila spp. developing in the petioles of Heracleum mantegazzianum Sommier & Levier (giant hogweed). Additionally, it shows attraction to Phallus impudicus L. (common stinkhorn), but was never recovered from it in situ. Not attracted to fermenting fruit. Rarely collected in Malaise traps or by sweep netting.
Flight period. July to September.
Host. Mainly Drosophila limbata Roser, 1840 and other species within the Drosophila quinaria species group ( van Alphen et al. 1991; Eijs and van Alphen 1999).
Ex situ reared from Drosophila kuntzei Duda, 1924 and Scaptomyza pallida (Zetterstedt, 1847) , and to a lesser degree from Drosophila transversa Fallén, 1823 ( van Alphen et al. 1991). Not reared from D. busckii Coquillett, 1901 , D. immigrans Sturtevant, 1921 , D. phalerata Meigen, 1830 , D. subobscura Collin, 1936 , and Lordiphosa fenestrarum Fallén, 1823 , despite sharing the ecological niche with the suitable hosts ( van Alphen et al. 1991).
Population parameters. Primarily thelytokous with occasional development of males, observed after ex situ diapause by van Alphen et al. (1991).
Distribution.
Western Palearctic but sparsely distributed, possibly spreading towards northwest but slowly and still uncommon. Armenia (locus typicus of Rhoptromeris australis ), Belgium (new record), Denmark, the Netherlands and Slovenia.
Remarks.
Originally described in the genus Rhoptromeris Förster, 1869 but moved to Leptopilina Förster, 1869 by Nordlander and Grijpma (1991).
We did not successfully sequence any specimen of L. australis . At present, barcode sequence information is available neither on BOLD nor on DROP.
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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Cynipoidea |
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Eucoilinae |
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Genus |
Leptopilina australis (Belizin, 1966)
| Vogel, Jonathan, Martin, Jakob, Forshage, Mattias, Salden, Tobias, Staverløkk, Arnstein, Verheyde, Fons, Nordlander, Göran, Herz, Annette & Peters, Ralph S. 2025 |
Rhoptromeris australis
| Rhoptromeris australis Belizin, 1966: 87 . |
