Research Article |
Corresponding author: Mao-Ling Sheng ( shengmaoling@163.com ) Academic editor: Bernardo Santos
© 2019 Xi-Nan Wang, Mao-Ling Sheng, Martin Schwarz.
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:
Wang X-N, Sheng M-L, Schwarz M (2019) A new species of genus Hoplocryptus Thomson (Hymenoptera, Ichneumonidae, Cryptinae) and a key to species from Oriental and Eastern Palaearctic regions. ZooKeys 865: 21-29. https://doi.org/10.3897/zookeys.865.35094
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A new species of Cryptinae, Hoplocryptus qingdaoensis Sheng, Wang & Schwarz, sp. nov. collected from Qingdao, Shandong Province, in the north border of oriental part of China, is described and illustrated. A key to species known from the Oriental and Eastern Palaearctic regions is provided.
Agrothereutina, Cryptini, Eastern Palaearctic region, key, Oriental region, taxonomy
Hoplocryptus Thomson, 1873 belongs to the tribe Cryptini of the subfamily Cryptinae (Hymenoptera: Ichneumonidae), and comprises 32 species (
In the last two years the first two authors have been exploring the mountains in Qingdao (Laoshan Natural Reserve), Shandong Province, situated along the Yellow Sea in the northern border of the Oriental part of China, and have collected large numbers of ichneumonids. In this article, one new species, collected in this area is described.
Specimens were collected with interception traps (IT) proposed by
The type specimen of Hoplocryptus savioi Uchida, 1940, deposited in the Institute of Zoology, Chinese Academy of Sciences, Beijing, P.R. China, was examined. The photos of the types of Aritranis ohgushii Momoi, 1963, A. pini Momoi, 1973, Caenocryptus alboanalis Uchida, 1952, C. tamahonis Uchida, 1931, Hoplocryptus nigripes chinensis Uchida, 1952, H. sugiharai Uchida, 1936 and H. sumiyona Uchida, 1956 (deposited in the Hokkaido University Museum and Museum of Nature and Human Activities, Sanda, Hyogo, Japan) taken by Dr. Kyohei Watanabe (Kanagawa Prefectural Museum of Natural History, Odawara, Japan: KPMNH), were checked and compared to the new species by the corresponding author.
Images were taken using a Leica M205A Stereomicroscope with LAS Montage MultiFocus. Morphological terminology is mostly based on
Type specimens are deposited in the Insect Museum, General Station of Forest and Grassland Pest Management (GSFGPM), National Forestry and Grassland Administration, People’s Republic of China.
Hoplocryptus Thomson, 1873: 508.
Hoplocryptus binotatulus Thomson, 1873 (= murarius Börner, 1782).
Ventral margin of clypeus with a more or less distinct tooth or tubercle (rarely somewhat paired). Mesoscutum with distinct punctation on a polished or subpolished background. Fore wing with sides of areolet subparallel or moderately narrowed anteriorly. Often both transverse carinae of propodeum entirely developed. Dorsolateral carina of first metasomal tergite usually distinct basal of spiracle (best seen in dorsal or dorsolateral view), its postpetiole rather weakly convex dorsally and not or only rather weakly wider than petiole. Second tergite with distinct and usually moderate sized punctures. Ovipositor compressed and its tip with rather regular and subvertical ridges on lower valve.
This genus morphologically resembles Aritranis in having sides of areolet parallel or moderately convergent anteriorly, 2m-cu straight or more or less sinuate, hind wing with M+Cu moderately to strongly arched, lateral longitudinal carina of propodeum absent, first metasomal segment without a lateral tooth basally and with its spiracle at or not very far behind its mid-length; but it can be distinguished from the latter by its dorsolateral carina of first metasomal tergite usually distinct basad of spiracle (best seen in dorsal or dorsolateral view), its postpetiole rather weakly convex dorsally, ventral margin of clypeus with a more or less distinct tooth (rarely paired teeth). Hosts are aculeate Hymenoptera. Aritranis: dorsolateral carina of first gastral tergite absent (or more rarely indistinct) basal of spiracle, postpetiole rather distinctly convex dorsally, ventral margin of clypeus without a tooth, except in the Aritranis nigripes group. Hosts are Lepidoptera and Coleoptera as far as known.
This key does not include H. egregius (Kokujev, 1909) as its female is unknown.
1 | Clypeus with broad, blunt apical median tooth which has often a slight depression medially. Distance from vein 2rs-m to 2m-cu shorter than distance from 2m-cu to 3rs-m. Scutellum and median portion of hind tarsus often white. Tergites 2 and 3 red | H. confector (Gravenhorst) |
– | Clypeus with a narrow and pointed tooth, more rarely the tooth is somewhat blunt, tooth never with a depression medially. Differ often in other characters | 2 |
2 | Mesopleuron, mesosternum, propodeum and first tergite black, at most with white flecks | 3 |
– | At least parts of propodeum, mesopleuron, mesosternum, or first tergite red or reddish yellow | 13 |
3 | Areolet convergent anteriorly. Ventral tooth of mandible as long as dorsal tooth. Tergites with dense large punctures. Mesosoma entirely black (sometimes red). Tergites 2–3(4) yellowish red | H. heliophilus (Tschek) |
– | Not entirely as above; if areolet convergent forward, then ventral tooth of mandible distinctly longer than dorsal tooth. Tergites with weak, fine punctures. Mesosoma with yellowish white spots. Tergites with distinct white spots | 4 |
4 | Lower tooth of mandible distinctly longer than upper tooth. Head posteriorly to eyes as seen from above strongly narrowed. Areolet convergent forward. Ovipositor tip long and comparatively low, about 4 times as long as high | H. murarius (Börner) |
– | Lower tooth of mandible usually as long as upper tooth. Head posteriorly to eyes as seen from above evenly narrowed. Areolet with vein 3rs-m approximately parallel to 2rs-m (except H. alboanalis). Ovipositor tip relatively short | 5 |
5 | Apical portion of dorsal valve of ovipositor (Fig. |
H. qingdaoensis Sheng, Wang & Schwarz, sp. nov. |
– | Apical portion of dorsal valve of ovipositor without tubercles (except H. ohgushii), rarely with indistinct one or two swellings. Transverse carinae of propodeum weak, posterior carina vestigial, or median portion of posterior transverse carina strongly bended forwards. Face entirely black. Tergites almost entirely black. Hind coxae unicolor | 6 |
6 | Metasomal tergites 2, 3, and hind leg black (hind femur of H. quadriguttatus red) | 7 |
– | Tergites 2, 3 and hind femur reddish brown | 12 |
7 | Apical portion of scutellum white. Hind femur and tibia red | H. quadriguttatus (Gravenhorst) |
– | Scutellum and hind femur and tibia black (basal portion of H. sugiharai white) | 8 |
8 | Gena, mesosoma and metasomal tergites entirely covered with very dense and relatively large punctures. Hind wing vein 1-cu shorter than cu-a | H. savioi Uchida |
– | Gena, mesosoma and metasomal tergites with fine, relatively sparse punctures, at least tergites 4 to 6 with indistinct, fine punctures. Hind wing vein 1-cu at least as long as cu-a | 9 |
9 | Area basalis large, triangular. Distance between anterior transverse carina and posterior end of propodeum 3 times as long as distance from anterior transverse carina to anterior margin of area basalis. Apical portions of scutellum and first tergite and posterolateral portion of second tergite with white spots | H. ohgushii (Momoi) |
– | Area basalis relatively small, trapezoidal. Length between anterior transverse carina and posterior end of propodeum at least 4 times as long as distance from anterior transverse carina to anterior margin of area basalis. Scutellum, first and second tergites without white spots | 10 |
10 | Posterior transverse carina of propodeum complete, strongly arched forward medially. Area basalis distinctly longer than its width. Fore wing with vein 1cu-a opposite 1/M. Areolet convergent forward. Hind wing vein 1-cu 2.2 times as long as cu-a | H. alboanalis (Uchida) |
– | Posterior transverse carina of propodeum weak, slightly arched forward medially. Area basalis about as long as its width. Fore wing with vein 1cu-a basad of 1/M. Areolet with vein 3rs-m parallel to 2rs-m. Hind wing vein 1-cu at most 1.5 times as long as cu-a | 11 |
11 | Clypeus with dense punctures. Area basalis distinctly trapezoidal, strongly convergent backwardly. Tegula and hind tibia entirely black | H. scorteus (Momoi) |
– | Clypeus smooth, almost without punctures. Area basalis almost quadrate, nearly not convergent backwardly. Tegula and basal portion of hind tibia white | H. sugiharai Uchida |
12 | Ovipositor sheath longer than hind tibia. Basal portion of clypeus with dense fine punctures. Tergites 2 and 3 with dense and large punctures. Hind coxa black | H. femoralis (Gravenhorst) |
– | Ovipositor sheath distinctly shorter than hind tibia. Clypeus shiny, basal portion with relative sparse fine punctures. Tergites with finely rugate and punctures. Hind coxa sometimes red | H. coxator (Tschek) |
13 | Mesosoma 2.0–2.1 times as long as its maximum height. First tergite strongly arched medially. Hind coxa entirely brownish red. Posterior portions of tergites 2 and 3 with wide transverse white bands | H. tamahonis (Uchida) |
– | Mesosoma at most 1.9 times as long as its maximum height. First tergite arched distinctly beyond its middle. Hind coxa mainly black, at least apical portion more or less darkish. Tergites 2 and 3 without white bands | 14 |
14 | Antenna without white spot. Mesoscutum and mesopleuron usually orange. Hind coxa mainly black. Tergites 2 and 3 of metasoma almost entirely black | H. bellosus (Curtis) |
– | Antenna with white spot. Mesoscutum and at least anterior portion of mesopleuron black. Hind coxa mainly brown to reddish brown. Tergites 2 and 3 of metasoma orange to reddish brown | 15 |
15 | Mesoscutum with distinct punctures. Apical 0.7 of fore tibia strongly swollen. Posterior portion of mesopleuron brown | H. pini Momoi |
– | Mesoscutum extensively granulated. Fore tibia evenly, slightly swollen apically. Mesopleuron entirely black | H. bohemani (Holmgren) |
The specific name is derived from the type locality.
Holotype. Female, CHINA: Laoshan, Qingdao, Shandong Province, 12 June 2017, IT. Paratype. 1 female, same data as holotype except 26 June 2017.
Propodeum rather long. Metasomal tergites 3–6 with even dense and unclear punctures. Second metasomal tergite (Figs
Hoplocryptus qingdaoensis Sheng, Wang & Schwarz, sp. nov. Holotype, female 1 habitus, lateral view 2 head, anterior view 3 head, lateral view 4 head, dorsal view 5 mesoscutum 6 mesosoma, lateral view 7 propodeum 8 metasoma, dorsal view 9 second to fourth tergites 10 apical portion of ovipositor, lateral view.
Female. Body length 11.0 to 11.9 mm. Fore wing length 7.0 to 7.4 mm. Ovipositor sheath length 2.3 to 2.4 mm.
Inner margins of eyes slightly convergent ventrally. Face (Fig.
Anterior portion of pronotum with dense yellowish white hairs, lateral concavity (Fig.
(Figs
(Fig.
This new species is similar to Hoplocryptus alboanalis (Uchida, 1952) by the characters: Clypeus with a strong smooth blunt tubercle medially; notaulus strong on anterior half of mesoscutum. anterior and posterior transverse carinae of propodeum complete; ventral valve of ovipositor with strong edges; mesosoma almost entirely black; median portion of flagellum, at least ventral profiles, white; and can be distinguished from the latter by the following combination of characters: Fore wing vein cu-a basad of Rs & M by about 0.3 times length of cu-a. Posterior transverse carina of propodeum (Fig.
The authors are deeply grateful to Drs Bernardo Santos (Department of Entomology, National Museum of Natural History, Washington, USA), Kyohei Watanabe (KPMNH), and Seung-Ho Oh (Research and Planning Division, National Science Museum, Republic of Korea) for reviewing this manuscript. The authors are also indebted to Drs Kyohei Watanabe (KPMNH) for taking the photos of Hoplocryptus types deposited in Japan, Kui-Yan Zhang (Institute of Zoology, Chinese Academy of Sciences, Beijing, P.R. China) and Masahiro Ohara (Hokkaido University Museum, Hokkaido University, Japan) for their help while the corresponding author was working in their respective museums. This research was supported by the National Natural Science Foundation of China (NSFC, No. 31501887, No. 31310103033) and Forestry Science and Technology lnnovative Program of Shandong (LYCX09-2018-44).