Research Article |
Corresponding author: Shi-Xiang Zong ( zongsx@126.com ) Corresponding author: Mao-Ling Sheng ( shengmaoling@163.com ) Academic editor: Gavin Broad
© 2021 Shu-Ping Sun, Tao Li, Shi-Xiang Zong, Mao-Ling Sheng.
This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Citation:
Sun S-P, Li T, Zong S-X, Sheng M-L (2021) Two new species of Anisotacrus Schmiedeknecht (Hymenoptera, Ichneumonidae, Ctenopelmatinae) with a key to Eastern Palaearctic species. Journal of Hymenoptera Research 82: 187-197. https://doi.org/10.3897/jhr.82.64742
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Two species of genus Anisotacrus Schmiedeknecht, 1913, A. externus Sheng & Sun, sp. nov. and A. senticosus Sheng & Sun, sp. nov., collected from the Natural Reserve, Huairou, Beijing, are described and illustrated. A key to the Eastern Palaearctic species of Anisotacrus is provided.
China, Euryproctini, taxonomy
Anisotacrus Schmiedeknecht, 1913, a small genus of the tribe Euryproctini in the subfamily Ctenopelmatinae (Hymenoptera: Ichneumonidae), comprises nine species (
Five species from Russia (
The most reliable-looking host records for Anisotacrus are from grass-feeding sawflies of the genus Dolerus (
In this paper two species of Anisotacrus from China with a key to known species from the Eastern Palaearctic region are reported.
Specimens were collected by interception traps (IT) (Li et al. 2012) in the Natural Reserve, Huairou, Beijing, China.
Morphological terminology is mostly based on
Anisotacrus Schmiedeknecht, 1913: 2710. Type-species: Mesoleius tenellus Holmgren, 1857.
(After
1 | First tergite and hind coxa red. Face predominantly yellow | A. kurilensis Kasparyan, 2007 |
– | First tergite and hind coxa black. Face black or ivory | 2 |
2 | Face black. Tergites, hind leg except trochantellus, black. First tergite 1.7 × as long as posterior width | A. konishii Kasparyan, 2007 |
– | Face entirely or at least laterally white or yellow. Tergites and hind leg at least partly reddish brown or yellow. First tergite at least 2.0 × as long as posterior width | 3 |
3 | Face black, laterally yellow. Mesosoma black. Tergites 2–4 (5) red or with reddish brown spots. Areolet receiving vein 2m-cu basal of its lower posterior corner | 4 |
– | Face white. Propleuron and spot on upper portion of epicnemium whitish yellow. Second and subsequent tergites reddish brown, if posterior tergites black, then vein 2m-cu slightly distal of areolet (Figs |
6 |
4 | Frons with wrinkles. Hind wing vein 1-cu approximately as long as cu-a. Tergitrs 2 and 3 with wrinkles | A. bipunctatus (Gravenhost, 1829) |
– | Frons shagreened, or with fine punctures. Hind wing vein 1-cu distinctly longer than cu-a. Tergites 2 and 3 shagreened, or with fine punctures | 5 |
5 | First tergite 2.7 × as long as posterior width. Mesoscutum, fore and mid coxae, trochanters and femur entirely black. Basal half of hind tibia brownish yellow. Hind tarsus black | A. senticosus Sheng & Sun, sp. nov. |
– | First tergite at most 2.5 × as long as apical width. Anterolateral spot of mesoscutum yellow. Fore and mid coxae and trochanters black, with yellow spots. Hind femur apically and tibia black. Hind tarsus brown | A. xanthostigma (Gravenhorst, 1829) |
6 | Malar space 0.9 × as long as basal width of mandible. Areolet receiving vein 2m-cu basal of its lower posterior corner. Hind coxa, tergite 2 and subsequent tergites reddish brown | A. albinotatus Kasparyan, 2007 |
– | Malar space 0.6 × as long as basal width of mandible. Vein 2m-cu distal of areolet (Figs |
A. externus Sheng & Sun, sp. nov. |
Body length 6.0 mm. Fore wing length 4.6 mm. Ovipositor sheath 0.5 mm long.
Head. Inner margins of eyes (Fig.
Mesosoma. Anterior margin of pronotum (Fig.
Metasoma. First tergite (Figs
Coloration
(Fig.
The specific name is derived from the fore wing vein 2m-cu connecting to cubitus distal of lower-posterior corner of areolet.
Holotype : China • ♀; Beijing, Huairou, Labagoumen; 9.VII.2016; IT by Shi-Xiang Zong.
China.
The new species is similar to A. albinotatus Kasparyan, 2007, but can be distinguished from the latter by the following combination of characters: malar space about 0.6 × as long as basal width of mandible; areolet triangular, 2m-cu connecting to cubitus slightly distal of areolet (Fig.
Body length 8.7 mm. Fore wing length 6.9 mm. Ovipositor sheath 0.5 mm.
Head. Inner margins of eyes (Fig.
Anisotacrus senticosus Sheng & Sun, sp. nov. Holotype. Female 14 head, anterior view 15head, lateral view 16 head, dorsal view 17 mesoscutum, dorsal view 18 mesosoma, lateral view 19 hind tibia, lateral view 20 first tergite, dorsal view 21 second and third tergites, dorsal view 22 apical portion of metasoma, lateral view.
Mesosoma. Pronotum, mesoscutum, mesopleuron and metapleuron shagreened, almost entirely with fine indistinct punctures. Epomia present. Mesoscutum (Fig.
Metasoma. First tergite (Fig.
Coloration
(Fig.
The specific name is derived from the tibia with thorns.
Holotype : China • ♀; Beijing, Huairou, Labagoumen; 15.VIII.2016; IT by Shi-Xiang Zong.
China.
The new species is similar to A. xanthostigma (Gravenhorst, 1829), but can be distinguished from the latter by the following combination of characters: areolet distinctly quadrilateral; first tergite evenly convex, without longitudinal groove; second tergite as long as apical width; third tergite distinctly shorter than its width; mesoscutum, tegulae, all coxae and trochanters black. Anisotacrus xanthostigma: areolet triangular; first tergite with longitudinal groove; second tergite longer than apical width; third tergite as long as apical width; anterolateral portion of mesoscutum with yellow spots; tegulae yellow; fore coxae and parts of trochanters yellow.
The male of Anisotacrus xanthostigma displays some distinct variation (
The authors are deeply grateful to Drs Gavin Broad (The Department of Life Sciences, the Natural History Museum, London, UK), Matthias Riedel (Zoologische Staatssammlung München, Munich, Germany) and Andrei E Humala (Forest Research Institute, Karelian Research Centre, Russian Academy of Sciences, Petrozavodsk, Russia) for reviewing this manuscript. The authors are also indebted to Drs Dmitri Kasparyan and Andrey I. Khalaim (Zoological Institute, Russian Academy of Sciences, St. Petersburg, Russia) for presenting valuable material. This research was supported by National Key Research & Development Program of China “Research on key technologies for prevention and control of major disasters in plantation” (2018YFD0600200), the National Natural Science Foundation of China (NSFC, No. 31110103062, No. 31501887) and by key project of Science-technology basic condition platform from The Ministry of Science and Technology of the People’s Republic of China (Grant No. 2005DKA21402).