Research Article |
Corresponding author: Mao-Ling Sheng ( shengmaoling@163.com ) Academic editor: Gavin Broad
© 2021 Tao Li, Guo-Bin Chang, Zai-Hua Yang, Shu-Ping Sun, Yü Tian, 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:
Li T, Chang G-B, Yang Z-H, Sun S-P, Tian Y, Sheng M-L (2021) Two new species of Cymodusa Holmgren (Hymenoptera, Ichneumonidae) with a key to species known from China and Oriental region. Journal of Hymenoptera Research 88: 103-114. https://doi.org/10.3897/jhr.88.75304
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Two new species of genus Cymodusa Holmgren, 1859, C. culaiica Sheng, Li & Sun, sp.nov. collected from Culaishan Natural Reserve, Shandong province and C. melana Sheng, Li & Sun, sp.nov. collected from Guiyang and Fanjingshan National Natural Reserve, Guizhou province, are described and illustrated. A taxonomic key to the species of Cymodusa from China and the Oriental region is provided.
Campopleginae, new species, Key, taxonomy
Cymodusa Holmgren, 1859 (Hymenoptera, Ichneumonidae, Campopleginae) comprises 43 species (
The Oriental species of Cymodusa Holmgren and a key to the known species from this region were reported by Gupta & Gupta (1974). The Palaearctic species of Cymodusa were revised by
Ten host species of Cymodusa, mainly belonging to families Crambidae, Gelechiidae, Geometridae, Erebidae, Pyralidae, Yponomeutidae, have been recorded (
In this paper two new species of Cymodusa and a key to known species from China and the Oriental region are reported.
Specimens were collected by interception traps (IT) (
Images were taken using a Leica M205A stereomicroscope with LAS Montage MultiFocus. Morphological terminology is based on
Cymodusa Holmgren, 1859:327. Type-species: Cymodusa leucocera Holmgren.
Eyes with setae. Inner margins of eyes weakly indented opposite antennal socket. Face strongly convergent ventrally (especially in female). Mandible short, lower edge with a narrow flange, or as a high carina; upper tooth usually as long as lower tooth. Malar space very short, or absolutely wanting in female. Posterior transverse carina of mesosternum complete. Propodeal spiracle circular. Glymma absent. Ovipositor stout, compressed, almost straight.
1 | Hind wing nervellus not intercepted, discoidella absent | 2 |
– | Hind wing nervellus intercepted, discoidella present, usually unpigmented | 4 |
2 | Malar space 0.25–0.26× basal width of mandible. Anterior tentorial pit distinctly distant from eyes. Metasomal tergites entirely black. Proximal flagellomeres white | C. antennator Holmgren, 1860 |
– | Malar space at most 0.15× basal width of mandible. Anterior tentorial pit almost obscured. At least part of metasomal tergites red to brownish red. Flagellomeres almost entirely black | 3 |
3 | Area basalis (Fig. |
C. culaiica Sheng, Li & Sun, sp.nov. |
– | Area basalis relatively short, at most 2.0× as long as anterior width. Antenna with 29–34 flagellomeres. Hind leg mostly brownish black | C. orientalis Uchida, 1956 |
4 | Area basalis, area superomedia and area petiolaris of propodeum completely confluent. Areolet receiving 2m-cu distinctly basal of its middle. Fourth tergite entirely red. Tegula yellowish white. Hind coxa black | C. dravida Gupta & Gupta, 1974 |
– | At least area basalis distinctly separated from area superomedia by transverse carina. Areolet receiving 2m-cu almost at its middle. Fourth tergite entirely or partly black. Tegula and hind coxa with different coloration | 5 |
5 | Area basalis of propodeum with lateral carinae parallel, 3.0× as long as wide. Area externa finely rugose. Hind coxa and all metasomal tergies black | C. taprobanicum (Cameron, 1905) |
– | Area basalis of propodeum at most 2.0× as long as wide, more or less convergent. Area externa with different sculpture. Hind coxa or metasomal tergites (except C. melana) not entirely black | 6 |
6 | Malar space 0.25–0.35× basal width of mandible. Postocellar line 0.9–1.0 × as long as ocular-ocellar line. Hind basitarsus 2× as long as hind tibial spur. Hind coxa and femur black | C. shiva Gupta & Gupta, 1974 |
– | Malar space wanting, or at most 0.15× basal width of mandible. Postocellar line at least 1.2× as long as ocular-ocellar line. Hind basitarsus at least 2.3× as long as hind tibial spur. Hind coxa and femur (except C. melana) not entirely black. | 7 |
7 | Tergite 2 granulose in anterior portion, posterior portion and subsequent tergites subpolished. Tergites 2–4 with posterior transverse red bands | C. santoshae Gupta & Gupta, 1974 |
– | Tergites 2 and 3 granulose. Metasomal tergites entirely or almost entirely black | 8 |
8 | Dorsal median portion of occipital carina evenly arched. Lateral carinae of area basalis convergent posteriorly, 2× as long as wide. Tergite 2 as long as tergite 1. 1cu-a opposite M&RS. Claw pectinate subbasally. Posterior margin of tergite 2 red | C. josephi Gupta & Gupta, 1974 |
– | Dorsal median portion of occipital carina (Fig. |
C. melana Sheng, Li & Sun, sp.nov. |
Head, mesosoma and all tergites coriaceous. Anterior tentorial pit obscure, against eye. Areolet sessile (Fig.
Body length 4.0–5.0 mm. Fore wing length 2.2–2.5 mm. Ovipositor sheath 0.8–1.0 mm.
Head. Head with coriaceous surface. Eye (Figs
Mesosoma. Lateral concavity of pronotum (Figs
Metasoma. First tergite (Fig.
Coloration
(Fig.
The specific name is derived from the type locality.
Holotype : China • ♀; Shandong, Chashankou, Culaishan Natural Reserve, Tai’an; 2.VI.2018; IT by Tao Zhao. Paratypes: China • 13♀♀; same data as for holotype except 26.V.–9.VI.2018.
China.
The new species is similar to C. orientalis Uchida, 1956, but can be distinguished easily from the preceding key.
Dorsal median portion of occipital carina (Fig.
Body length 7.0–7.5 mm. Fore wing length 3.5–4.0 mm. Ovipositor sheath 1.2–1.5 mm.
Head. Eye with weak, short setae, inner margins (Fig.
Mesosoma. Lateral concavity of pronotum (Figs
Metasoma. First tergite (Fig.
Coloration
(Fig.
The specific name is derived from the body and hind leg almost entirely black.
Holotype : China • ♀; Guizhou, Lengjiaba, 840 m, Fanjingshan National Natural Reserve, Jiangkou; 24.VI.2019; IT by Zhen-Hai Yang. Paratypes: China • 1♀; same data as for holotype. • 1♀; same data as for holotype except 23.IX.2019. China • 2♀♀; Guizhou, Panlongshan, 1179 m, Wudang, Guiyang; 24.VI.2019; IT by Zai-Hua Yang.
China.
The new species is similar to C. taprobanica (Cameron, 1905), but can be distinguished from the latter by the following combination of characters: areolet sessile; area basalis of propodeum at most 1.7× as long as maximum width; area superomedia wider than length; hind leg almost entirely black. Cymodusa taprobanica (Cameron): areolet petiolate; area basalis of propodeum about 3.0× as long as wide; area superomedia longer than width; hind leg partly black.
According to Watanabe’s report (Watanabe, 2020), the area basalis of the propodeum of Cymodusa orientalis Uchida, 1956 shows strong variation: slightly to strongly convergent posteriorly, even triangular (also see Dbar, 1985). The original description of C. josephi stated that the hind wing nervellus is intercepted; in C. orientalis the hind wing nervellus is not intercepted; and the character of area basalis of propodeum is within the range of C. orientalis. The specimens in our collections, collected from Guangxi, Guizhou and Jiangxi, located at the north border of Oriental region, and Shandong and Sichuan, located at the south border of the Eastern Palaearctic region, almost entirely with same characters, except some of them have the nervellus obscurely intercepted, the remainder with the nervellus not intercepted. For a decision, the types of C. josephi Gupta & Gupta, 1974, C. orientalis Uchida, 1956, C. aenigma Dbar, 1985 and more similar material should be studied in the future, or more accurate assessments will be helped by molecular methods.
The authors are deeply grateful to Drs Gavin Broad (Department of Life Sciences, the Natural History Museum, London, UK), Kyohei Watanabe (Kanagawa Prefectural Museum of Natural History, Kanagawa, Japan) and Matthias Riedel (Zoologische Staatssammlung München, München, Germany) for reviewing this manuscript. The authors also thank Dr. Kyohei Watanabe for sending some type photos of Cymodusa orientalis Uchida, 1956, and Yang Li, Tao Zhao (Culaishan Forest Farm, Tai’an, Shandong, China) and Zhen-Hai Yang (Fanjingshan National Natural Reserve, Jiangkou, Guizhou, China) for their help in the course of exploration in Shandong and Guizhou Provinces. This research was supported by National Animal Collection Resource Center, China and by the National Natural Science Foundation of China (NSFC, No. 31501887, No. 31110103062).