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Research Article
Four new species of Gasteruption Latreille from NW China, with an illustrated key to the species from Palaearctic China (Hymenoptera, Gasteruptiidae)
expand article infoJiang-Li Tan, Cornelis van Achterberg, Qing-Qing Tan, Xue-xin Chen§
‡ Northwest University, Xi’an, China
§ Zhejiang University, Hangzhou, China
Open Access

Abstract

Four new species of the genus Gasteruption Latreille, 1796 (Hymenoptera: Evanioidea: Gasteruptiidae: Gasteruptiinae) are reported from NW China: three from Shaanxi province and one from Ningxia province. The new species (G. bicoloratum Tan & van Achterberg, sp. n., G. huangshii Tan & van Achterberg, sp. n., G. pannuceum Tan & van Achterberg, sp. n., and G. shengi Tan & van Achterberg, sp. n.) and three newly recorded species (G. sinepunctatum Zhao, van Achterberg & Xu, 2012, G. boreale (Thomson, 1883) and G. oshimense Watanabe, 1924) are keyed and fully illustrated. In total, seven species are known from Shaanxi province, which is approximately half of the expected number. The East Palaearctic specimens provisionally identified as G. tournieri Schletterer, 1885, by Zhao et al. (2012) are included under G. oshimense Watanabe, 1924.

Keywords

Gasteruption , Heilongjiang, Inner Mongolia, key, Mongolia new species, new record, Ningxia, Shaanxi

Introduction

The family Gasteruptiidae is a small group of wasps comprising about 500 described species in two subfamilies, Gasteruptiinae (four genera) (Macedo 2009, 2011; Zhao et al. 2012) and Hyptiogastrinae (two genera) (Jennings and Austin 2002). Gasteruptiidae are easily distinguished from the other apocritan hymenopterans by the elongated “neck” (propleuron), the swollen hind tibiae, and the highly attached and slender metasoma. Adults are free-living insects normally feeding on nectar from flowers with easily accessible nectar (especially families Apiaceae, Asteraceae and Euphorbiaceae), but likely at least some Gasteruption species feed on both nectar and pollen (Jennings and Austin 2004). Gasteruptiidae are also known by their hovering inspection flight in front of bee nests (van Achterberg 2013). The larvae feed on the larval food of solitary bees, after consuming the egg or larva of the bee (Malyshev 1966). They select bees of the subfamilies Apinae, Colletinae and Megachilinae nesting in stems or in wood, and less often in clay banks or other vertical soil substrates (Malyshev 1965; Zhao et al. 2012; van Achterberg 2013); as far as known, bees nesting in horizontal soil substrates are far less attacked. However, in Australia members of the Hyptiogastrinae do attend bee nests in flat ground (Houston 1987). There is only indirect evidence that Gasteruptiinae may attack wasp nests, especially of Crabronidae, Sphecidae and solitary Vespidae (Eumeninae) (Crosskey 1951; Gauld and Hanson 1995, Hanson and Gauld 2006; Jennings and Austin 1997a, 1997b, 2004). Metamorphosis takes place inside the host’s nest where the gasteruptiid pupa hibernates until the next spring or summer (Malyshev 1968; He 2004; Jennings and Austin 2004). All known gasteruptiids from the Palaearctic Region belong to the subfamily Gasteruptiinae and to the genus Gasteruption Latreille, 1796. For identification the revision of the Chinese species (Zhao et al. 2012) and the yet unpublished revision of the East Palaearctic species (van Achterberg, in prep.) were used. According to Zhao et al. (2012) two species (G. angulatum Zhao, van Achterberg & Xu, 2012 and G. japonicum Cameron, 1888) are known from the NW Chinese province Shaanxi, which is 7% of the total of 28 species reported from China. Italy (about as varied in natural habitats as Shaanxi) is 50% larger than Shaanxi but has 20 species reported, which is about 60% of the total species known from Europe. In this paper we report five additional species, and from the comparison with Italy it may be deduced these seven are about half of the number to be expected.

Material and methods

The specimens were mainly collected by hand net or sweep netting, rarely in Malaise traps during 2015. Specimens from Shaanxi were directly stored in 70% ethanol, prepared using the AXA method (van Achterberg 2009; van Achterberg et al. 2010) and glued on card points; other specimens were directly pinned. Observations and descriptions were made with an Olympus SZX11 stereomicroscope and fluorescent lamps. Photographic images were made either with a Keyence VHX-5000 digital microscope or with an Olympus motorized stereomicroscope SZX12 and processed with Adobe Photoshop CS5, mostly to adjust the size and background.

Figure A–B. 

Measurements (A) of the relative length of the propleuron (a) and length of the mesoscutum in front of the tegulum (b) and (B) the length and maximum width of the basal antennal segments; asc = antesternal carina.

For comparison of head shapes it is essential that the middle of the vertex is in plane of objective of binocular microscope. For the other terminology, see Zhao et al. (2012) and van Achterberg (1988). Measurements are performed as indicated in Fig. A–B and in van Achterberg (1988). Additional non-exclusive characters in the key are between square brackets. The association of males with females is based on similarity. In the few cases in which no males were available, distinctive, and probably non-sexual, characters of the female were tentatively used for inclusion in the key. A new provincial record is indicated by an asterisk. The following abbreviations are used for the depositories:

ECHU Entomology Collection, Hokkaido University, Sapporo

NWUX College of Life Sciences, Northwest University, Xi’an

RMNH Naturalis Biodiversity Center, Leiden

ZJUH Parasitic Hymenoptera Collection of the Zhejiang University, Hangzhou

Results

Gasteruption Latreille, 1796

Gasteruption Latreille, 1796: 113; Zhao et al. 2012: 6–7 (diagnosis, references, key); van Achterberg 2013: 59 (illustrated key for the Netherlands); Jennings and Parslow 2014: 95; van Achterberg and Talebi 2014: 10 (illustrated key for Iran and Turkey); Žikić et al. 2014: 573. Type-species (designated by Latreille 1810): Ichneumon assectator Linnaeus, 1758.

Key to species of the genus Gasteruption Latreille from Palaearctic China

1 Ovipositor present (a); antenna with 14 segments (b) (females) 2
Ovipositor absent (aa); antenna with 13 segments (bb) (males); [if males are unknown the species is provisionally included, see Materials and methods] 32
2 Apex of ovipositor sheath entirely blackish or dark brown, OR, if narrowly pale apically, then white, ivory or brownish yellow part at most 0.3 times as long as hind basitarsus (a); (intermediate species are included in both alternatives) 3
Apex of ovipositor sheath distinctly white or ivory (but rarely pale brown) and pale part 0.3–8.0 times as long as hind basitarsus (aa) 21
3 Ovipositor sheath 0.6–1.9 times as long as hind tibia and 0.3–1.2 times as long as hind tibia and tarsus combined (a); incision of hypopygium shallow, V-shaped and extending to apical 0.2 (b); occipital carina obsolescent to narrowly lamelliform medio-dorsally (c) 4
Ovipositor sheath 3.0–7.0 times as long as hind tibia and 1.9–4.0 times as long as hind tibia and tarsus combined (aa); incision of hypopygium often deep and slit-like and extending to apical 0.3–0.5 (bb); occipital carina obsolescent (c) or distinctly lamelliform (cc) medio-dorsally 14
4 Malar space in anterior view 0.5–0.6 times length of pedicellus and 0.4–0.6 times basal width of mandible and mandibular condylus distinctly below lower level of eyes (a); in lateral view condylar incision of malar space remains far removed from eye (b); ovipositor sheath 0.4–0.9 times as long as hind tibia (c); first discal cell of fore wing usually suddenly narrowed (d) G. oriplanum Kieffer, 1914
Head in anterior view slightly protruding below lower level of eyes by less than half basal width of mandible and mandibular condylus near lower level of eyes (aa); in lateral view condylar incision of malar space close to eye (bb); ovipositor sheath 0.8–2.7 times as long as hind tibia (cc); first discal cell of fore wing usually gradually narrowed (dd) 5
5 Clypeus with rather large shallow depression (a); mesoscutum densely reticulate-rugulose or -rugose (b); hind basitarsus stout (c); apical antennal segment 1.4–1.6 times third antennal segment (d) G. formilis Alekseev, 1995
Clypeus with small depression or depression obsolescent (aa); mesoscutum mainly densely coriaceous or rugulose (bb); hind basitarsus slender (cc), rarely similarly stout; apical antennal segment at most 1.2 times as long as third antennal segment (dd) 6
6 Mesoscutum coarsely (often “crater”-like) punctate (a); head distinctly emarginate medio-posteriorly (b); head less protruding in lateral view (c) and narrower in anterior view (d) 7
Mesoscutum predominantly densely coriaceous, at most with some shallow punctures (aa); head truncate medio-posteriorly or nearly so (bb); head more protruding in lateral view (cc) and wider in anterior view (dd) 8
7 Hind tibia about as long as hind femur and trochanter combined or slightly longer (a); head somewhat longer in dorsal (b) and lateral (c) view; head directly narrowed behind eyes in dorsal view (d) G. formosanum Enderlein, 1913
Hind tibia 1.1–1.2 times as long as hind femur and trochanter combined (aa); head somewhat shorter in dorsal (bb) and lateral (cc) view; head roundly narrowed behind eyes in dorsal view (dd) G. sinicola (Kieffer, 1924)
8 Hind tibia comparatively slender (a); side of pronotum slender and with narrow and weakly crenulated grooves (b); propleuron granulate antero-dorsally (c); [hind basitarsus slender; vertex distinctly punctulate or very finely coriaceous] G. parvicollarium Enderlein, 1913
Hind tibia distinctly inflated (aa); side of pronotum robust and with wider and distinctly crenulated grooves (bb); propleuron rugulose or coriaceous antero-dorsally (cc) 9
9 Mandible dark brown or reddish brown basally (a), rarely brownish yellow; basal depression of mandible rather large and deep (b); fifth (= pre-apical) sternite dark brown or blackish or narrowly pale medio-apically (c) 10
Mandible pale yellow basally (aa); basal depression of mandible often smaller and shallower (bb); fifth sternite yellowish brown medio-apically (cc) 12
10 Vertex matt or with satin sheen and densely coriaceous (a); mesoscutum densely coriaceous and without indication of punctures (b); head gradually narrowed posteriorly in dorsal view (c); antero-ventral tooth of pronotum absent or indistinct (d); [third antennal segment 1.5–1.7 times as long as pedicellus; ovipositor sheath only with short fine setae] 11
Vertex shiny and punctulate (aa); mesoscutum with some fine punctures (bb); head directly narrowed posteriorly in dorsal view (cc); antero-ventral tooth of pronotum distinct (dd); [occipital carina distinct medio-dorsally] G. latitibia Zhao, van Achterberg & Xu, 2012
11 Apical half of ovipositor sheath with dense and adpressed setosity (a); sculpture of mesoscutum distinctly coarser than that of vertex (b); ovipositor sheath 1.1–1.3 times as long as hind tibia (c); head more narrowed behind eyes in dorsal view (d) (Linnaeus, 1758)
Apical half of ovipositor sheath with erect bristles, angled at about 45º (aa); sculpture of mesoscutum slightly coarser than that of vertex (bb); ovipositor sheath 0.7–1.0 times as long as hind tibia (cc); head less narrowed in dorsal view (dd) G. boreale (Thomson, 1883)
12 Head longer and directly narrowed in dorsal view (a); posteriorly vertex moderately convex in lateral view (b); metasoma mainly black or dark brown (c); tegula dark brown (d) G. terebrelligerum Enderlein, 1913
Head shorter and less directly narrowed in dorsal view (aa); vertex flattened in lateral view (bb); metasoma with distinctly yellowish pattern (cc); tegula yellow (dd) 13
13 Head not protruding below eyes (a) and malar space 0.3 times length of second antennal segment and 0.2 times basal width of mandible and mandibular condylus close to lower level of eyes (b); hind basitarsus rather stout and at least partly ivory dorsally (c); hind tibia dark ventrally, similar to colour dorsally (d); mesoscutum somewhat coarser sculptured (e) G. flavimarginatum van Achterberg, 2014
Head somewhat protruding below eyes (aa) and malar space 0.5 times length of second antennal segment and 0.4 times basal width of mandible and mandibular condylus below lower level of eyes (bb); hind basitarsus slender and entirely dark brown dorsally (cc); hind tibia ventrally paler than dorsally (dd); mesoscutum finely sculptured (ee) G. bicoloratum sp. n.
14 Vertex with reversed V-shaped emargination medio-posteriorly (a), flat (b) and smooth, shiny and long dorsally (c); mesoscutum mainly moderately transversely rugose (d) G. bimaculatum Pasteels, 1958
Vertex truncate medio-posteriorly (aa) or reversed U-shaped emarginate (aaa), shorter and moderately convex (bb); if vertex more or less emarginate and/or flat, then vertex finely sculptured, with satin sheen and shorter (cc); mesoscutum punctate, punctate-rugose or transversely wrinkled (dd) 15
15 Head rather elongate and below eyes slightly enlarged, minimum length of malar space 0.3–0.4 times second antennal segment (a); head distinctly reversed U-shaped emarginate medio-posteriorly (b); mandible brown (c); hind tarsus brownish apically, paler than basally (d); [apex of ovipositor sheath ivory; first metasomal tergite orange or yellowish brown] G. dimidiatum Semenov, 1892
Head less elongate and below eyes not enlarged, minimum length of malar space 0.1–0.2 times second antennal segment (aa); head shallowly emarginate medio-posteriorly (bb); if intermediate (bbb) then mandible brownish yellow (cc); apically hind tarsus dark brown as basally (dd); [apex of ovipositor sheath dark brown or black] 16
16 Hind tibia slender (a); hind femur black or blackish brown (b); middle lobe of mesoscutum finely sculptured (c); scapus ventrally and third antennal segment black (d); [length of ovipositor sheath 3–6 times as long as hind tibia; scutellum coriaceous] 17
Hind tibia distinctly inflated (aa); hind femur orange brown to dark brown (bb); middle lobe of mesoscutum punctate or punctate-rugose (cc); scapus ventrally paler than third antennal segment or both dark brown (dd) 18
17 Middle lobe of mesoscutum transversely wrinkled (a); apex of ovipositor sheath ivory (b); apical half of hypopygium largely blackish (c); [ovipositor sheath about 3 times as long as hind tibia] G. pannuceum sp. n.
Middle lobe of mesoscutum coriaceous between punctures (aa); apex of ovipositor sheath blackish (bb); apical half of hypopygium brown (cc) or yellowish brown; [ovipositor sheath 4–6 times as long as hind tibia] G. shengi sp. n.
18 Apex of ovipositor sheath ivory, brownish-yellow or brown and pale part 0.3–1.0 times as long as hind basitarsus (a); mesosoma sparsely setose laterally (b); hind femur dark brown or brown (c); [ovipositor sheath 4.8–6.0 times as long as hind tibia] G. sinarum Kieffer, 1911
Apex of ovipositor sheath mainly dark brown (aa), pale part at most 0.3 times as long as hind basitarsus; mesosoma densely setose laterally (bb); hind femur orange or reddish brown (cc); [head darker than mesoscutum anteriorly] 19
19 Ovipositor sheath 3.1–4.4 times as long as hind tibia (a); mesoscutum often bicoloured (b); vertex densely setose (c); mesosoma largely or entirely black laterally (d); [hind femur and tibia (except basally) similarly coloured, orange brown or dark brown] G. dilutum Semenov, 1892
Ovipositor sheath about 7.0 times as long as hind tibia (aa); mesoscutum unicoloured (bb); vertex sparser setose (cc); mesosoma dark reddish or orange brown laterally (dd) 20
20 Ventral half of outer side of hind tibia dark brown or blackish except well differentiated subbasal ivory part (a); basal half of hind coxa mainly transversely rugose dorsally (b); apex of ovipositor sheath dark brown (c); propleuron, mesoscutum and pronotum similarly dark brown (d) G. coloratum Zhao, van Achterberg & Xu, 2012
Outer side of hind tibia partly reddish brown and ivory subbasal part less defined (aa); basal half of hind coxa superficially coriaceous dorsally (bb); apex of ovipositor sheath ivory or brownish yellow (cc); mesoscutum and pronotum distinctly paler than propleuron (dd) G. argentifrons Semenov-T.-S. & Kostylev, 1928
21 Head with comparatively wide medial depression in front of occipital carina and with pair of lateral depressions (a); occipital carina wide lamelliform (b); medially mesoscutum distinctly transversely punctate-rugulose (c) G. oshimense Watanabe, 1934
Head flat or evenly convex in front of occipital carina (aa), if with a shallow depression in front of occipital carina (aaa), then occipital carina at most moderately lamelliform (bb) and mesoscutum with coarser transverse rugae or punctation medially (cc) 22
22 Ovipositor sheath comparatively wide and about 0.9 times as long as hind tibia, 0.3 times as long as metasoma and 0.2 times as long as body (a); middle lobe of mesoscutum rather protuberant in lateral view (b); pronotal tooth slender and acute G. assectoides Zhao, van Achterberg & Xu, 2012
Ovipositor sheath comparatively narrow and 1.1–9.0 times as long as hind tibia, 0.6–2.8 times as long as metasoma and 0.4–1.4 times as long as body (aa); middle lobe of mesoscutum less protuberant in lateral view (bb); if convex (bbb) then pronotal tooth wider and rather blunt (cc) 23
23 Ovipositor about 0.4 times as long as body and 0.6 times as long as metasoma (a); hind coxa very slender (b); ovipositor widened apico-ventrally and more or less angularly up curved apically in dead specimens (c) G. angulatum Zhao, van Achterberg & Xu, 2012
Ovipositor 0.8–1.4 times as long as body and 1.2–1.9 times as long as metasoma (aa); hind coxa slightly less slender (bb); ovipositor narrow apico-ventrally and nearly straight or gradually up curved apically (cc) 24
24 Pale apical part of ovipositor sheath 3.0–3.5 times as long as hind basitarsus (a); vertex shiny and largely smooth or finely punctulate (b); fourth antennal segment 1.7–2.3 times as long as third antennal segment (c); mesoscutum more or less coarsely spaced punctate or punctate-rugose medio-posteriorly (d) G. tonkinense Pasteels, 1958
Pale apical part of ovipositor sheath 0.3–3.2 times as long as hind basitarsus (aa); if 2.8–3.2 times (G. japonicum) then head dorsally with satin sheen and distinct fine sculpture (bb); fourth antennal segment 1.2–1.9 times as long as third antennal segment (cc); mesoscutum punctate, transverse rugose, punctate-rugose or partly reticulate medio-posteriorly (dd) 25
25 Hind femur and tibia widened (a); hind basitarsus robust (b); head slightly narrowed in dorsal view (c); head slender in anterior view (d) and face narrower than clypeus (e); hind basitarsus entirely dark brown (f); [ovipositor sheath about 1.4 times as long as body and 8.5 times as long as hind tibia] G. huangshii sp. n.
Hind femur and tibia slender (aa); hind basitarsus slender (bb); head in dorsal view distinctly narrowed (cc); head in anterior view subglobular (dd), if slender (ddd) then face as wide as clypeus (ee); hind basitarsus often partly ivory (ff) 26
26 Mesoscutum punctulate between rather coarse punctures (a); head slimmer in anterior view (b); [pale apical part of ovipositor sheath up to about 0.3 times as long as hind basitarsus; metasoma entirely orange or yellowish brown, at most darkened apically; ovipositor sheath 1.0–1.3 times as long as body] 27
Mesoscutum coriaceous between punctures (aa) or coriaceous-punctulate; head in anterior view less slender (bb) 28
27 Mesosoma dorsally (a), hind coxa (b) and femur (c) reddish or orange brown; hind basitarsus mainly ivory (d) G. argentifrons Semenov T.-S. & Kostylev, 1928
Mesosoma dorsally black (aa), hind coxa (bb), hind femur (cc) and hind basitarsus (dd) dark brown G. dimidiatum Semenov, 1892
28 Pale apical part of ovipositor sheath 0.3–1.0 times as long as hind basitarsus (a); occipital carina non-lamelliform medio-dorsally (b) and mesoscutum coarsely punctate or rugose (c) G. sinarum Kieffer, 1911
Pale apical part of ovipositor sheath 1.1–3.2 times as long as hind basitarsus (aa); occipital carina narrow lamelliform medio-dorsally (bb), if non-lamelliform (bbb) then mesoscutum very finely coriaceous or rugulose (cc) 29
29 Anterior half of mesoscutum normally coriaceous and with distinct punctures (a); head dorsally with satin sheen and micro-sculptured (b); head slightly narrowed in dorsal view (c) G. poecilothecum Kieffer, 1911
Anterior half of mesoscutum very finely and densely coriaceous, without (aa) or with punctures (aaa), rarely very finely transversely rugulose; head dorsally more or less shiny and smooth (bb), at most very finely punctulate; head directly narrowed posteriorly in dorsal view (cc) 30
30 Occipital carina fine and non-lamelliform dorsally (a); vertex in front of occipital carina without depression (b); head rather stout in dorsal view (c); mesoscutum at most punctulate, usually hardly or not punctate (d) G. sinepunctatum Zhao, van Achterberg & Xu, 2012
Occipital carina narrow lamelliform dorsally (aa); vertex in front of occipital carina with indistinct depression (bb); head slimmer in dorsal view (cc); mesoscutum more or less punctate (dd) 31
31 Mesoscutum moderately punctate (a); hind coxa rather robust basally (b); white or ivory apical part of ovipositor sheath 1.4–2.2 times as long as hind basitarsus (cc); [hind basitarsus often partly ivory] G. japonicum Cameron, 1888
Mesoscutum at most finely punctate (aa); hind coxa slimmer basally (bb); white or ivory apical part of ovipositor sheath 2.1–3.2 times as long as hind basitarsus (cc) G. rufescenticorne Enderlein, 1913

Males

32 Vertex with distinct medio-posterior depression or a groove with two minute tubercles in front of distinctly lamelliform occipital carina (a); mesoscutum medially transversely or obliquely rugulose, in large specimens transversely rugose (b); occipital carina wide lamelliform (c) G. oshimense Watanabe, 1934
Vertex flat or evenly convex in front of occipital carina (aa), if slightly depressed (aaa) then mesoscutum mainly punctate medially (bb) or occipital carina narrow lamelliform (cc) 33
33 Clypeus with rather large shallow depression (a); hind basitarsus rather stout (b); mesoscutum reticulate or rugose (c); [head and scapus more or less orange or reddish-brown, but sometimes entirely black] G. formilis Alekseev, 1995
Clypeus with small depression or depression obsolescent (aa); hind basitarsus often slimmer (bb) or mesoscutum coriaceous or rugulose (cc) 34
34 Head in anterior view distinctly protruding below lower level of eyes (a), in lateral view condylar incision of malar space remains distinctly removed from eye, malar area behind indentation square and at least 0.8 times as long as second antennal segment (= pedicellus) and 0.7–0.9 times basal width of mandible (b); mesoscutum densely coriaceous and matt, similar to vertex (c) G. oriplanum Kieffer, 1914
Head in anterior view hardly protruding below lower level of eyes (aa), in lateral view condylar incision of malar space close to eye and malar area behind indentation transverse and 0.3–0.5 times as long as second antennal segment and 0.2–0.3 times basal width of mandible (bb); if malar space slightly enlarged then mesoscutum punctate or transversely rugose and rather shiny, different from vertex (cc) 35
35 Mesoscutum only coriaceous or finely rugulose medially (a), at most with a few shallow punctures; [G. assectoides provisionally included, ♂ unknown] 36
Mesoscutum with several distinctly impressed punctures medially (aa; but often shallow in G. japonicum) or reticulate-rugose (aaa) 47
36 Hind tibia slender, hardly to moderately inflated (a); mesoscutum often very finely and regularly sculptured (b) 37
Hind tibia distinctly inflated (aa); mesoscutum mainly densely coriaceous or irregularly rugulose (aa), especially near notauli (bb) 42
37 Mesoscutum distinctly regularly transversely rugulose (a); hind tibial spurs yellowish and distinctly contrasting with dark hind basitarsus (b) G. assectoides Zhao, van Achterberg & Xu, 2012
Mesoscutum mainly finely coriaceous or superficially irregularly rugulose (aa); hind tibial spurs more or less brown and less contrasting with hind basitarsus (bb) 38
38 Fourth antennal segment 2.5–3.5 times as long as third segment (a); face rather narrow (b) 39
Fourth antennal segment 1.4–1.7 times as long as third segment (aa; unknown of G. pannuceum); face wide (bb) 40
39 Fourth antennal segment about 3.5 times as long as third segment (a); second and third antennal segments robust (b); hind femur and tibia slender (c) G. sinepunctatum Zhao, van Achterberg & Xu, 2012
Fourth antennal segment about 2.5 times as long as third segment (aa); second and third antennal segments slender (bb); hind femur and tibia rather robust (cc) G. huangshii sp. n.
40 Head strongly convex in lateral and anterior view (a); head long in dorsal view (b); hind coxa and tibia rather robust (c) G. parvicollarium Enderlein, 1913
Head moderately convex in lateral and anterior view (aa); head rather short in dorsal view (bb); hind coxa and tibia slender (cc) 41
41 Mandible largely dark brown (a); hind coxa and femur elongate (b) G. angulatum Zhao, van Achterberg & Xu, 2012
Mandible yellowish brown (aa); hind coxa and femur less elongate (bb); [occipital carina non-lamelliform medio-dorsally] G. pannuceum sp. n.
42 Frons and vertex shiny and smooth (a); mesoscutum rugose medio-posteriorly (b) and near notauli (c) G. latitibia Zhao, van Achterberg & Xu, 2012
Frons and vertex matt or with satin sheen, micro-sculptured (aa); mesoscutum coriaceous or rugulose near notauli (bb) and medio-posteriorly rugulose (cc) or mainly punctate 43
43 Mandible pale yellowish basally (a); apex of paramere yellowish brown (b); apical metasomal sternites yellowish posteriorly (c) G. flavimarginatum van Achterberg, 2014
Mandible brown, dark brown or black basally (aa); apex of paramere dark brown or blackish (bb); apical metasomal sternites dark brown or black posteriorly (cc) 44
44 Head longer and rather trapezoid in dorsal view (a); hind tibia broadly darkened basally (b) G. terebrelligerum Enderlein, 1913
Head shorter and transverse in dorsal view (aa); hind tibia yellowish or narrowly darkened basally (bb) 45
45 Hind tibia strongly inflated (a); head less narrowed posteriorly in dorsal view (b); basal antennal segments slightly more robust (c) 46
Hind tibia less inflated (aa); head slightly more narrowed posteriorly in dorsal view (bb); basal antennal segments slightly slimmer (c) G. bicoloratum sp. n.
46 Mesoscutum distinctly more coarsely sculptured than vertex (a); head directly narrowed behind eyes (b); malar space short (c) G. assectator (Linnaeus, 1758)
Mesoscutum slightly more coarsely sculptured than vertex (aa); head less narrowed behind eyes (bb); malar space more or less enlarged (cc) G. boreale (Thomson, 1883)
47 Posteriorly vertex flat in lateral view and long (a); head smooth and shiny dorsally (b); head moderately narrowed posteriorly (c); mesosoma laterally often paler than dorsally (d) G. bimaculatum Pasteels, 1958
Posteriorly vertex convex in lateral view and usually shorter (aa); sculpture of head dorsally variable (bb), if smooth (bbb) them more narrowed posteriorly (cc); mesosoma usually unicoloured (dd) or dorsally paler than laterally 48
48 Hind coxa orange brown or dark brown (a); mesoscutum rather densely setose (b); metasoma largely reddish brown (c); [mandible orange yellow or yellowish brown; mesoscutum finely or coarsely punctate and often with narrow interspaces] 49
Hind femur black (aa); mesoscutum less densely setose (bb); metasoma often largely dark brown or black (cc) 51
49 Mesoscutum finely punctate, with rather wide interspaces (a); hind tibia yellowish brown or indistinctly infuscate basally (b); apical half of hind basitarsus partly dark brown and only apically ivory (c) G. dilutum Semenov, 1892
Mesoscutum coarsely punctate and interspaces narrower (aa); hind tibia distinctly dark brown basally (bb); apical half of hind basitarsus mainly ivory (cc) 50
50 Basal half of hind coxa rugose dorsally (a); outer side of hind tibia (except basally) dark brown or blackish (b); head subtruncate posteriorly in dorsal view (c) G. coloratum Zhao, van Achterberg & Xu, 2012
Basal half of hind coxa superficially coriaceous dorsally (aa); ventral half of outer side of hind tibia orange-brown (bb); head emarginate posteriorly in dorsal view (cc) G. argentifrons Semenov-T.-S. & Kostylev, 1928
51 Third antennal segment robust (a); ventral half of pronotal side largely superficially coriaceous to nearly smooth, only grooves crenulated (b); pronotum partly densely setose (c) 52
Third antennal segment slender (aa); ventral half of pronotal side largely moderately reticulate-rugose, at most ventrally coriaceous (bb); pronotum sparsely setose (cc) 53
52 Malar space narrow (a); head less emarginate medio-posteriorly (b); mesoscutum usually with less coarse sculpture (c); scutellum mainly micro-sculptured (d), at most with few large punctures G. shengi sp. n.
Malar space slightly wider (aa); head distinctly emarginate medio-posteriorly (bb); mesoscutum with coarser sculpture (cc); scutellum coarsely punctate (dd) G. dimidiatum Semenov, 1892
53 Hind tibia distinctly inflated (a); head directly narrowed posteriorly in dorsal view (b); third antennal segment slender, 1.6–1.9 times as long as second segment (c); [mesoscutum distinctly “crater-like” punctate; head concave medio-posteriorly] 54
Hind tibia slender (aa); head usually gradually narrowed posteriorly in dorsal view (bb); third antennal segment robust, 1.2–1.7 times as long as second segment (cc) 55
54 Hind tibia strongly inflated (a); third antennal segment less slender (b) G. sinicola (Kieffer, 1924)
Hind tibia moderately inflated (aa); third antennal segment slender (bb) G. formosanum Enderlein, 1913
55 Occipital carina moderately wide (a); vertex distinctly convex (b); [middle lobe of mesoscutum coarsely punctate laterally] G. tonkinense Pasteels, 1958
Occipital carina narrow lamelliform or non-lamelliform (aa); vertex comparatively flat (bb) 56
56 Occipital carina narrow lamelliform (a) and slightly depressed in front of it medio-dorsally (b); mesoscutum less coarsely punctate (c) G. japonicum Cameron, 1888
Occipital carina less or non-lamelliform (aa) and flat medio-dorsally (bb); mesoscutum more or less coarsely punctate (cc) 57
57 Head slightly enlarged below eyes in anterior view (a); medium-sized punctures of mesoscutum not connected to form transverse elements (b); lateral lobe of mesoscutum largely finely coriaceous and rather matt, more or less punctate (c) G. poecilothecum Kieffer, 1911
Head not enlarged below eyes in anterior view (aa); large punctures of mesoscutum connected to transverse rugae or part of reticulation (bb); lateral lobe of mesoscutum more coarsely coriaceous or rugose and with satin sheen (cc) G. sinarum Kieffer, 1911

Systematics

Gasteruption angulatum Zhao, van Achterberg & Xu, 2012

Figs 1–6

Gasteruption angulatum Zhao et al., 2012: 19–22 (description).

Material

1♂ (NWUX), China: Shaanxi, Mt. Qin, Baolongyu, N34°03' E108°09', 10.vi.2015, 24.v.2015, Jiangli Tan.

Figures 1–6. 

Gasteruption angulatum Zhao, van Achterberg & Xu, 2012, male, Shaanxi. 1 habitus lateral 2 mesosoma dorsal 3 hind leg lateral 4 head dorsal 5 basal antennal segments 6 apex of metasoma lateral.

Gasteruption bicoloratum Tan & van Achterberg, sp. n.

Figs 7, 8–16, 17–22

Type material

Holotype, ♀ (NWUX), “China: Shaanxi, Foping, Yueba, Qinling Mts, N33°32' E107°49', 27.vi1.vii.2015, 1095 m, Qingqing Tan”. Paratypes: 4♀3♂ (NWUX, RMNH), same data as holotype.

Comparative diagnosis

Runs in Zhao et al. (2012) to G. oriplanum Kieffer, 1911 (but the malar space is shorter in the new species and oblique in anterior view, not subparallel-sided below eyes in anterior view as in G. oriplanum and the mandibles are paler) or to G. assectator (Linnaeus, 1758). The pale fifth sternite of the female, the strongly narrowed head in dorsal view, the shorter ovipositor sheath (about 0.6 times hind tibia vs 0.9–1.3 times in G. assectator) and the yellowish mandible separate it from G. assectator. The new species is close to G. flavimarginatum van Achterberg, 2014, but it has a slightly longer malar space (short in G. flavimarginatum), the hind basitarsus slender and dorsally dark brown (rather robust and at least partly ivory dorsally) and the mesoscutum finely sculptured (coarser sculptured). The male differs by having the apex of the paramere dark brown, which is yellowish brown in G. flavimarginatum.

Description

Holotype, female, length of body 9.9 mm, of fore wing 4.9 mm.

Head. Vertex and frons with satin sheen, finely coriaceous, moderately convex and without a depression medio-posteriorly; head directly contracted behind eyes in dorsal view and temples nearly straight (Fig. 14); temple 0.9 times as long as eye in dorsal view; fourth antennal segment 1.2 times as long as third segment and 0.7 times as long as second and third segments combined, fifth antennal segment as long as third segment, third antennal segment 1.6 times as long as second segment (Fig. 8); occipital carina narrow and non-lamelliform medio-dorsally (Fig. 8); OOL 1.3 times as long as diameter of posterior ocellus; face wide, 2.8 times as broad as high, 2.4 times as wide as eye in frontal view (Fig. 13); malar space somewhat protruding below lower level of eyes (Fig. 13), its minimum width 0.4 times as long as second antennal segment and 0.35 times basal width of mandible and area behind incision nearly square (Fig. 8); clypeus only medio-ventrally shallowly depressed (Fig. 13); eye with numerous short setae.

Figure 7. 

Gasteruption bicoloratum Tan & van Achterberg, sp. n., female, holotype, habitus lateral.

Figures 8–16. 

Gasteruption bicoloratum Tan & van Achterberg, sp. n., female, holotype. 8 head lateral 9 mesosoma lateral 10 mesosoma dorsal 11 fore wing 12 apex of metasoma lateral 13 head anterior 14 head dorsal 15 hind leg 16 ovipositor and ovipositor sheath lateral.

Mesosoma. Length of mesosoma 1.6 times its height; propleuron robust and 0.8 times as long as mesoscutum in front of tegulae; pronotal side entirely coriaceous except for crenulated grooves and sparsely setose, without acute tooth antero-ventrally (Figs 8–10); antesternal carina narrow and hardly lamelliform; mesosternal sulcus wide and deep; mesoscutum and scutellum rather matt and superficially rugulose-coriaceous (Fig. 10); propodeum reticulate-rugose and without median carina.

Wings. First discal cell parallel-sided and with outer posterior corner rounded, and with vein 3-CU1 near its apical third (Fig. 11).

Legs. Hind coxa finely granulate-coriaceous; length of hind femur, tibia and basitarsus 3.9, 3.6 and 4.6 times their width, respectively; hind tibia strongly inflated (Fig. 15); middle tarsus 1.1 times as long as middle tibia; middle femur subparallel-sided and slimmer than fore femur.

Metasoma. Ovipositor sheath 1.2 mm, 0.1 times as long as body, 0.2 times as long as metasoma and 0.6 times as long as hind tibia; ovipositor sheath with dense cover of fine brownish and adpressed setae, its apical half slender; hypopygium shallowly emarginate medio-posteriorly.

Colour. Black; apical half of antenna largely brown ventrally; mandible pale brownish yellow (except narrow dark borders); clypeus latero-ventrally and humeral plate dark brown; tegulum, second-seventh metasomal tergites narrowly apically and widely laterally, sixth sternite widely apically and other sternites narrowly, trochantelli, hind femur apico-ventrally and hind tibial spurs yellowish brown; fore and middle tibiae basally and hind tibia baso-ventrally widely ivory; remainder of legs, veins and pterostigma dark brown; wing membrane subhyaline.

Male. Similar to female (including fine sculpture of mesoscutum: Fig. 18); third antennal segment 1.3–1.6 times as long as second segment; fourth antennal segment 1.3–1.5 times as long as third segment and 0.8 times as long as second and third segments combined, fifth antennal segment 1.3–1.4 times as long as third segment (Fig. 21); apical sternite entirely dark brown; paramere densely whitish setose and its apex dark brown (Fig. 22).

Figures 17–22. 

Gasteruption bicoloratum Tan & van Achterberg, sp. n., male, paratype. 17 habitus lateral 18 mesosoma dorsal 19 mesonotum dorsal 19 hind leg 20 head dorsal 21 basal antennal segments lateral 22 apex of metasoma lateral.

Variation. Body length of ♀ 8.7–10.3 mm, of ♂ 8.2–9.9 mm; length of ovipositor sheath 0.6–0.7 times hind tibia; minimum width of malar space 0.3–0.4 times as long as second antennal segment; tibiae and tarsi more or less yellowish brown ventrally; apical antennal segment more or less obliquely depressed.

Distribution

China (Shaanxi). Montane: 1095 m.

Biology

Unknown. Collected JuneAugust.

Etymology

Named after the bicoloured hind tibia in both sexes (“bi” is Latin for “two”).

Gasteruption boreale (Thomson, 1883)

Figs 23, 24–32

Foenus borealis Thomson, 1883: 849; Hedicke 1939: 7; Hedqvist 1973: 181, 182 (invalid lectotype designation); Wall 1994: 148. Synonymized with G. assectator (Linnaeus) by Schletterer (1889) and with G. minutum (Tournier) by van Achterberg and Talebi (2014).

Gasteruption boreale ; Schletterer, 1885: 303; Johansson and van Achterberg (submitted; references and synonymy).

Trichofoenus breviterebrae Watanabe, 1934: 285; Hedicke 1939: 45. Synonymized with G. assectator (Linnaeus) by Pagliano and Scaramozzino (2000) and with G. boreale (Thomson) by Johansson and van Achterberg (submitted).

Type material

Holotype of G. breviterebrae, ♀ (ECHU), “[Russia,] Saghalien [= Sakhalin Oblast], K. Tamanuki/ Konuma, 23.v.1931”, “Holotype Trichofoenus breviterebrae Watanabe, 1934, det. Konishi”. Paratypes: 1 ♂ (ECHU), “[Russia,] Saghalien, K. Tamanuki/ Nagahama, 28.vii.1927”, “Paratype (Allotype) Trichofoenus breviterebrae Watanabe, 1934”.

Additional material

China (Heilongjiang, ZJUH); Russia (Sakhalin).

Diagnosis

(after Johansson and van Achterberg submitted) Head in dorsal view subparallel-sided behind eyes (Fig. 30), elongate, about as wide as long; occipital carina indistinct medio-dorsally; frons with satin sheen; mesoscutum rather weakly rugulose-coriaceous or chagreened, similar as vertex (Fig. 24) and with satin sheen, in front of scutellum rather rugose (Fig. 26); mesosoma and head silvery pilose; mesosoma with a satin sheen, quite distinct from the rather fatty gloss present in G. assectator s.s.; whitish pubescence of eye of female (Fig. 29) mostly distinctly longer and denser than of G. assectator s.s.; antenna slightly shorter than in G. assectator s.s. with sixth segment about 1.5 times longer than wide and subapical segment about 1.2 times longer than wide; only apical half of hind coxa weakly striate dorsally; hind tibia and basitarsus with white or ivory ring (Fig. 27); metasoma mainly black with orange lateral patches on tergites 2–4, which might be partially reduced (Fig. 23); inner sides of tibiae often red brown to orange with white or yellow basal patch indistinct on fore and middle tibiae; ovipositor sheath black or brown, 0.7–1.0 times as long as hind tibia, its apical half entirely with stout, rather scarce black bristles angled backwards at about 45° (Fig. 32). The male is difficult to separate from males of G. assectator s.s. and identification is not always possible with certainty. In most cases males of G. boreale have a slightly more elongate and subparallel-sided head in dorsal view, a less sculptured mesoscutum and a more or less enlarged malar space.

Figure 23. 

Gasteruption boreale (Thomson), female, holotype of G. breviterebrae (Watanabe), habitus lateral.

Figures 24–32. 

Gasteruption boreale (Thomson), female, holotype of G. breviterebrae (Watanabe). 24 head lateral 25 mesosoma lateral 26 mesonotum dorsal 27 hind leg 28 base of antenna 29 head anterior 30 head dorsal 31 fore wing 32 ovipositor and ovipositor sheath lateral.

Distribution

China (*Heilongjiang, ZJUH); Russia (Sakhalin). New for China.

Biology

Unknown. Collected May-July.

Gasteruption huangshii Tan & van Achterberg, sp. n.

Figs 33, 34–42, 43–48

Type material

Holotype, ♀ (NWUX), “China: Shaanxi, Hanzhong, Liuba, Zhang Liang Temple, N33.68° E106.83°, 28.vii.2015, 1348 m, Jiangli Tan & Qingqing Tan”. Paratypes (NWUX, RMNH): 5♂, same data as holotype.

Comparative diagnosis

The new species runs in the key by Zhao et al. (2012) to G. japonicum Cameron and G. sinepunctatum Zhao, van Achterberg & Xu, because of the very finely sculptured mesoscutum. It differs from both species by the trapezoid head in dorsal view (Fig. 40 vs Figs 55, 102), the distinctly widened hind tibia, fore and hind femora (Fig. 41 vs Figs 53, 103) and the slender head in anterior view (Fig. 39 vs Figs 54, 101). It shares with G. praestans Semenov-Tian-Shanskij & Kostylev, 1928, from Kazakhstan the widened hind femur and the sparsely punctate vertex. It differs by the ivory apical part of the ovipositor sheath (absent in G. praestans), the hind femur and basitarsus robust (slimmer), the mesoscutum finely coriaceous with fine punctures (coarsely and rather densely punctate) and the mesopleuron mainly coriaceous dorsally and posteriorly (reticulate).

Figure 33. 

Gasteruption huangshii Tan & van Achterberg, sp. n., female, holotype, habitus lateral.

Figures 34–42. 

Gasteruption huangshii Tan & van Achterberg, sp. n., female, holotype. 34 head lateral 35 mesosoma lateral 36 mesonotum dorsal 37 fore wing 38 hypopygium ventral 39 head anterior 40 head dorsal 41 hind leg 42 apex of ovipositor sheath.

Description

Holotype, female, length of body 12.5 mm, of fore wing 6.0 mm.

Head. Vertex and frons with satin sheen, finely and densely punctulate (but vertex with some fine additional punctures: Fig. 40), moderately convex and without a depression medio-posteriorly; head trapezoid and gradually narrowed behind eyes in dorsal view and temples convex (Fig. 40); temple 0.7 times as long as eye in dorsal view; fourth antennal segment 1.5 times as long as third segment and 0.9 times as long as second and third segments combined, fifth antennal segment 1.2 times as long as third segment (Fig. 33), third antennal segment 1.4 times as long as second segment; occipital carina narrow and narrowly lamelliform medio-dorsally (Figs 34, 40); OOL 1.3 times as long as diameter of posterior ocellus; face 2.7 times wider than high, 2.4 times wider than eye in anterior view (Fig. 39); minimum width of malar space 0.3 times as long as second antennal segment (Fig. 34); clypeus rather flat and with small round emargination medio-ventrally; eye glabrous.

Mesosoma. Length of mesosoma 2.1 times its height; propleuron rather robust and 0.9 times as long as mesoscutum in front of tegulae; pronotal side entirely punctulate (except for crenulated grooves and some fine punctures ventrally) and sparsely setose, with minute lobe-shaped tooth antero-ventrally (Fig. 35); antesternal carina narrow and hardly lamelliform; mesosternal sulcus narrow anteriorly and moderately wide posteriorly; mesopleuron mainly superficially coriaceous dorsally and posteriorly; mesoscutum and scutellum matt, very finely and superficially coriaceous with fine punctures and medio-posteriorly with some short grooves (Fig. 36); propodeum rugose anteriorly and coriaceous posteriorly.

Wings. First discal cell parallel-sided and with outer posterior corner rounded, and with vein 3-CU1 near apical third (Fig. 37).

Legs. Hind coxa very finely coriaceous-punctulate; length of hind femur, tibia and basitarsus 2.7, 3.5 and 4.1 times their width, respectively; middle tarsus 1.1 times as long as middle tibia; middle femur subparallel-sided and slimmer than distinctly widened fore femur.

Metasoma. Ovipositor sheath 15.3 mm, 1.2 times longer than body, 1.7 times as long as metasoma and 7.5 times as long as hind tibia, ivory apical part of sheath 1.8 times as long as hind basitarsus; apical half of hypopygium incised (Fig. 38).

Colour. Black; mandible dark brown with middle part brown; fore femur apically, fore and middle tibiae basally and apically, and hind tibial spurs yellowish brown; hind tibia ventro-basally ivory; tegulae and remainder of legs mainly dark brown; pterostigma dark brown; wing membrane subhyaline.

Male. Similar to female, but head behind eye slightly more contracted in dorsal view and somewhat shorter (Fig. 47); third antennal segment as long as second segment, fourth antennal segment 2.5–2.9 times as long as third segment and 1.3–1.5 times as long as second and third segments combined, fifth antennal segment 2.6–2.9 times as long as third segment (Fig. 46); mouthparts ivory; paramere densely whitish setose and its apex brownish yellow (Fig. 48).

Figures 43–48. 

Gasteruption huangshii Tan & van Achterberg, sp. n., male, paratype. 43 habitus lateral 44 mesosoma dorsal 45 hind leg 46 basal antennal segments 47 head dorsal 48 apex of metasoma lateral.

Variation. Body length of male 8.7–9.9 mm; sculpture of mesosoma of male very fine and only slightly coarser coriaceous than of female.

Distribution

China (Shaanxi).

Biology

Unknown, but the new species was collected together with a Hylaeus sp.

Etymology

Named after Huang Shi Gong (supposed teacher of the early Han general Zhang Liang), because the specimens were collected outside the hall with Huang Shi Gong’s statue at the Zhang Liang Temple.

Gasteruption japonicum Cameron, 1888

Figs 49, 50–57

Gasteruption japonicum Cameron, 1888: 134; Zhao et al. 2012: 58–61.

Gasteruption sinense var. minus Kieffer, 1924: 78; Zhao et al. 2012: 58 (synonymized with G. japonicum).

Material

2♀ (NWUX, RMNH), China: Shaanxi, Hanzhong, Nanzheng, Liping National Forest Park, N32°44'04” E106°36'34”, 22.vi.2015, c 1620 m, Jiangli Tan & C. van Achterberg; 1♀ (NWUX), China: Shaanxi, along the road from Hanzhong to Liping, N32.87° E106.71°, 4.ix.2015, c 1377 m, Jiangli Tan; 1♂ (NWUX), China: Hubei, Yichang, Yiling, Chentangping, Mal. trap, 17.v.10.vii.2015, c 465 m, Haoliang Ni; 1♀ (NWUX), China: Shaanxi, Foping, behind Biological Station, Malaise trap, N33°39'29” E107°48'25”, 29.v.19.vi.2016, c 1710 m, JL. Tan & C. v. Achterberg.

Notes

The lectotype female of Gasteruption rufescenticorne Enderlein, 1913, is obviously different from the paralectotype male (e.g. head not emarginate medio-posteriorly and more narrowed, narrower occipital carina and different sculpture of mesoscutum) and is very similar to G. japonicum. The differences as indicated in the key could be part of gradual variation and after examination of more Japanese material its status may need reconsideration.

Figure 49. 

Gasteruption japonicum Cameron, female, Japan, habitus lateral.

Figures 50–57. 

Gasteruption japonicum Cameron, female, Japan. 50 head lateral 51 mesosoma lateral 52 mesonotum dorsal 53 hind leg 54 head anterior 55 head dorsal 56 fore wing 57 apex of ovipositor sheath.

Gasteruption oshimense Watanabe, 1934

Figs 58, 59–67

Gasteruption oshimensis Watanabe, 1934: 283–284.

Gasteruption tournieri ; Zhao et al. 2012: 103–108.

Material

2♀ (NWUX), China: Shaanxi, Zhashui, Huanghualing., N33.76° E108.85°, 23.vii.2015, c 1577 m, Jiangli Tan; 2♂ (NWUX), China: Shaanxi, Hanzhong, Liuba, Zibai Mt. Nat. Res., N33.66° E106.78°, 5.ix.2015, c 1627 m, Jiangli Tan; 3♀ 6♂ (NWUX, RMNH), China: SE Shaanxi, Langoa near Ankang, N32°17'01” E109°03'46”, c 1100 m, Jiangli Tan, Qingqing Tan & C. van Achterberg; 1♂ (NWUX), China: Shaanxi, Foping, behind Biological Station, Malaise trap, N33°39'29” E107°48'25”, 29.v.19.vi.2016, c 1710 m, JL. Tan & C. v. Achterberg.

Notes

The East Palaearctic specimens provisionally identified as G. tournieri Schletterer, 1885, by Zhao et al. (2012) are included here under G. oshimense Watanabe. The different shape of the head was noticed before, but also the hind tibia and hind basitarsus are slimmer and the sculpture of the mesoscutum is less developed. Most likely it concerns a separate species and because a valid name is available, this name (correctly spelled as G. oshimense) is used here. Especially the size of the males is very variable, e.g. length of body is 5.3–8.7 mm in the series from Langoa collected at the same spot and within one hour.

Figure 58. 

Gasteruption oshimense Watanabe, female, lectotype, habitus lateral (ovipositor sheath missing).

Figures 59–67. 

Gasteruption oshimense Watanabe, female, lectotype. 59 head lateral 60 mesosoma lateral 61 mesonotum dorsal 62 hind leg 63 head anterior 64 head dorsal 65 occipital carina dorsal 66 fore wing 67 apex of ovipositor sheath.

Gasteruption pannuceum Tan & van Achterberg, sp. n.

Figs 68, 69–77

Type material

Holotype ♀ (NWUX), China: Shaanxi, Qinling Mts., Baolongyu, N34°03' E108°09', c 700 m, 10.vi.2015, 24.v.2015, Jiangli Tan.

Comparative diagnosis

Runs in Zhao et al. (2012) either to G. varipes (Westwood, 1851) (if the pale apical part of the ovipositor sheath is considered to be minor) or to G. sinarum Kieffer, 1911 (if the pale part is considered to be intermediate; Fig. 77). The new species differs from G. varipes by having the mesopleuron black and finely sculptured (orange brown and coarsely vermiculate-reticulate (rarely only weakly so)), the mesoscutum slender and finely rugulose (robust and coarsely rugose), the propodeum mainly coriaceous (coarsely vermiculate-rugose), a shorter ovipositor sheath (3 times hind tibia vs 5 times) and the mandible brownish yellow (blackish). The new species differs from G. sinarum by having a shorter ovipositor sheath (3.2 times hind tibia vs 4.8–6.0 times in G. sinarum), the mesoscutum without coarse punctures (present), the vertex shiny and largely smooth (with satin sheen and punctulate in G. sinarum) and the vertex distinctly convex (less so in G. sinarum). It shares with G. parvicollarium Enderlein, 1913, the convex vertex, but the new species has a longer ovipositor sheath (3.1 times hind tibia vs 1.2–1.7 times in G. parvicollarium), the mesoscutum transversely wrinkled (mainly coriaceous) and eyes more conspicuously setose.

Description

Holotype, female, length of body 10.0 mm, of fore wing 6.2 mm.

Head. Vertex and frons shiny and very finely punctulate, nearly smooth (Fig. 75), distinctly convex (Fig. 69) and without a depression medio-posteriorly; head trapezoid and directly narrowed behind eyes in dorsal view (Fig. 75); temple 0.7 times as long as eye in dorsal view; fourth antennal segment 1.1 times as long as third segment and 0.6 times as long as second and third segments combined, fifth antennal segment 1.2 times as long as third segment, third antennal segment 1.4 times as long as second segment; occipital carina narrow and non-lamelliform medio-dorsally (Figs 69, 75); OOL 1.5 times as long as diameter of posterior ocellus; face 3.5 times wider than high, twice wider than eye in anterior view (Fig. 74); minimum width of malar space 0.2 times as long as second antennal segment (Fig. 69); clypeus rather flat, slightly depressed ventrally and shallowly emarginate medio-ventrally; eye densely setose (Fig. 74).

Figure 68. 

Gasteruption pannuceum Tan & van Achterberg, sp. n., female, holotype, habitus lateral.

Figures 69–77. 

Gasteruption pannuceum Tan & van Achterberg, sp. n., female, holotype. 69 head lateral 70 mesosoma lateral 71 mesonotum dorsal 72 fore wing 73 hypopygium ventral 74 head anterior 75 head dorsal 76 hind leg 77 apex of ovipositor sheath.

Mesosoma. Length of mesosoma 2.1 times its height; propleuron rather robust and 0.9 times as long as mesoscutum in front of tegulae; pronotal side mainly coriaceous, but ventral half (except anteriorly) largely rugose and grooves crenulate and sparsely setose, with small blunt tooth antero-ventrally (Figs 70, 71); antesternal carina narrow and non-lamelliform; mesopleuron coriaceous and medially moderately rugose; mesosternal sulcus wide and crenulate; mesoscutum and scutellum with satin sheen, finely punctate-coriaceous, but middle lobe mainly transversely rugulose and medio-posteriorly broadly rugose (Fig. 71); propodeum mainly coriaceous but rugose anteriorly.

Wings. First discal cell parallel-sided and with outer posterior corner rounded, and with vein 3-CU1 near its apical third.

Legs. Hind coxa very finely coriaceous; length of hind femur, tibia and basitarsus 4.8, 5.1 and 5.1 times their width, respectively; middle tarsus 1.2 times as long as middle tibia; middle femur subparallel-sided and slightly slimmer than fore femur; hind tibia weakly inflated (Fig. 76).

Metasoma. Ovipositor sheath 8.5 mm, 0.8 times longer than body, 1.1 times as long as metasoma and 3.2 times as long as hind tibia, ivory apical part of sheath 0.3 times as long as hind basitarsus; apical 0.3 of hypopygium incised (Fig. 73).

Colour. Black; mandible brownish yellow and basally slightly darkened; apical antennal segment, apex of ovipositor sheath, fore and middle tibiae basally and hind tibia ventro-basally ivory or pale brown; penultimate antennal segment brown; tegulae, pterostigma, remainder of legs and antenna, hind tibial spurs and remainder of legs mainly dark brown or blackish; wing membrane subhyaline.

Male. Unknown.

Distribution

China (Shaanxi).

Biology

Unknown.

Etymology

Named after the rugulose (“wrinkled”) sculpture of the middle lobe of the mesoscutum: “pannuceus” is Latin for “wrinkled”.

Gasteruption shengi Tan & van Achterberg, sp. n.

Figs 78–79, 80–88, 89–94

Type material

Holotype, ♀ (NWUX), “China: Ningxia, Pingluo, Mt. Shizui, 25.v.2015, Mao-Ling Sheng”, “on Hedysarum scoparium Fisch ex Mey”. Paratypes: 1♀ 1♂ (RMNH), “N. China: Ningxia, Mt. Shizui, 6.v.2009, M.-L. Sheng, RMNH’11”; 1♂ (NWUX), “China: Inner Mongolia, Otog Banner, Yikebulage, 31.iii.2015, Mao-Ling Sheng”, “on Tetraena mongolica Maxim.” [translation of Chinese labels].

Comparative diagnosis

Runs in Zhao et al. (2012) to G. dimidiatum Semenov, 1892, because of the emarginate head, the long and black ovipositor sheath, punctate mesoscutum and the finely sculptured propodeum. The new species differs from G. dimidiatum by having the head not prolonged below eyes in anterior view and malar space 0.2–0.3 times as long as second antennal segment (head shortly prolonged below eyes in G. dimidiatum; fig. 107 in Zhao et al. 2012, malar space 0.4 times as long as second antennal segment), first metasomal tergite black (orange or yellowish brown), basal half of hind coxa only coriaceous (transversely rugulose), apex of ovipositor sheath black (narrowly ivory), mesoscutum rather finely punctate (somewhat coarser punctate) and slightly wider hind tibia (slightly narrower). Males may be confused with G. sinarum Kieffer, 1911, the latter species has the hind coxa distinctly transversely rugose, the hind tibia is slim and the mesoscutum is more or less rugulose.

Description

Holotype, female, length of body 13.1 mm, of fore wing 5.9 mm.

Head. Vertex and frons with satin sheen and very finely punctulate, but vertex posteriorly superficially coriaceous (Fig. 86), distinctly convex (Fig. 80) and without a depression medio-posteriorly; frons densely silvery setose anteriorly; head trapezoid and gradually narrowed behind eyes in dorsal view (Fig. 86); temple 0.7 times as long as eye in dorsal view; fourth antennal segment 1.4 times as long as third segment and 0.9 times as long as second and third segments combined, fifth antennal segment 1.1 times as long as third segment, third antennal segment 1.8 times as long as second segment; occipital carina narrow and hardly lamelliform medio-dorsally (Figs 80, 86); OOL 1.4 times as long as diameter of posterior ocellus; face 3 times wider than high, 2.2 times wider than eye in anterior view (Fig. 85); minimum width of malar space 0.2 times as long as second antennal segment (Fig. 80); clypeus rather flat, slightly depressed ventrally and distinctly emarginate medio-ventrally (Fig. 85); eye largely glabrous; head shallowly U-shaped emarginate posteriorly (Fig. 86).

Figures 78–79. 

Gasteruption shengi Tan & van Achterberg, sp. n., female holotype (78) and male paratype (79), habitus lateral.

Figures 80–88. 

Gasteruption shengi Tan & van Achterberg, sp. n., female, holotype. 80 head lateral 81 mesosoma lateral 82 mesonotum dorsal 83 fore wing 84 hypopygium lateral 85 head anterior 86 head dorsal 87 hind leg 88 apex of ovipositor sheath.

Mesosoma. Length of mesosoma twice its height; propleuron rather robust and 0.8 times as long as mesoscutum in front of tegulae; pronotal side mainly superficially coriaceous, with grooves crenulate and largely densely silvery setose, with small acute tooth antero-ventrally (Fig. 80); antesternal carina narrow and non-lamelliform; mesopleuron coriaceous and largely densely silvery setose; mesosternal sulcus rather wide and crenulate; mesoscutum and scutellum with satin sheen, mesoscutum rather coarsely punctate but interspace mostly wider than diameter of punctures, interspaces superficially coriaceous, but middle lobe medio-posteriorly with few rugae (Fig. 82); scutellum mainly superficially coriaceous and with few small punctures; propodeum mainly coriaceous but medially with transverse crenulation connected to smooth median area.

Wings. First discal cell parallel-sided and with outer posterior corner rounded and with vein 3-CU1 near its apical third (Fig. 83).

Legs. Hind coxa very finely coriaceous and with satin sheen; length of hind femur, tibia and basitarsus 4.6, 4.7 and 5.3 times their width, respectively; middle tarsus 1.2 times as long as middle tibia; middle femur subparallel-sided and slightly slimmer than fore femur; hind tibia moderately inflated (Fig. 87).

Metasoma. Ovipositor sheath 14.4 mm, 1.1 times longer than body, 1.6 times as long as metasoma and 5.9 times as long as hind tibia, apex of sheath black; apical 0.5 of hypopygium incised (Fig. 84).

Colour. Black; mandible brown and basally slightly darkened; base and apex of fore and middle tibiae, most of fore and middle basitarsi and subbasal ring of hind tibia ivory or pale brown; tegulae, base and apex of fore and middle femora, remainder of fore and middle tarsi (but middle telotarsus dark brown), hind tibial spurs, secondfifth metasomal segments, apical half of hypopygium and lateral spots on sixth tergite brown; pterostigma, veins and clypeus ventrally dark brown; wing membrane subhyaline.

Male. Similar to female, but sculpture of mesoscutum coarser (Fig. 90), head less emarginate posteriorly and propodeum more or less reticulate; third antennal segment 1.3 times as long as second segment, fourth antennal segment 1.9–2.1 times as long as third segment and 1.1–1.2 times as long as second and third segments combined, fifth antennal segment 1.9–2.3 times as long as third segment (Fig. 93); mouthparts partly ivory; paramere greyish setose and its apex black (Fig. 94); hind tarsus mainly dark brown or blackish.

Figures 89–94. 

Gasteruption shengi Tan & van Achterberg, sp. n., male, paratype from Inner Mongolia. 89 head lateral 90 mesosoma dorsal 91 hind leg 92 head dorsal 93 basal antennal segments 94 apex of metasoma lateral.

Variation. Body length of female 12.1–13.1 mm, of male 10.1–11.5 mm; length of malar space 0.2–0.3 times as long as second antennal segment; propleuron 0.8–0.9 times as long as mesoscutum in front of tegulae; ovipositor sheath 10.5–14.4 mm, 0.9–1.1 times longer than body, 1.4–1.6 times as long as metasoma and 4.1–5.9 times as long as hind tibia; occipital carina of female paratype narrow lamelliform medio-dorsally, mandible rather yellowish brown, hypopygium and sixth tergite entirely brown and seventh tergite laterally so, fore and middle legs (except coxae and trochanters) mainly brown, tegulae dark brown, hind femur brownish black and subbasal ring of hind tibia brownish.

Distribution

China (Ningxia, Inner Mongolia).

Biology

Unknown.

Etymology

Named after the collector, Prof. Dr Mao-Ling Sheng, for his contribution of our knowledge of Chinese parasitoid Hymenoptera.

Gasteruption sinepunctatum Zhao, van Achterberg & Xu, 2012

Figs 95, 96–104

Gasteruption sinepunctatum Zhao, van Achterberg & Xu, 2012: 85.

Material

1♀ (NWUX), China: Shaanxi, Hanzhong, Liuba, Zibai Mt. Nature Reserve, N33.66° E106.78°, 5.ix.2015, c 1627 m, Jiangli Tan.

Note

Known in China from Jilin, Zhejiang, Taiwan and Tibet; new for Shaanxi.

Figure 95. 

Gasteruption sinepunctatum Zhao, van Achterberg & Xu, female, Shaanxi, habitus lateral.

Figures 96–104. 

Gasteruption sinepunctatum Zhao, van Achterberg & Xu, female, Shaanxi. 96 head lateral 97 mesosoma lateral 98 mesonotum dorsal 99 fore wing 100 hypopygium ventral 101 head anterior 102 head dorsal 103 hind leg 104 apex of ovipositor sheath.

Acknowledgements

Thanks are due to Prof. Mao-ling Sheng (Shenyang) for the much appreciated gift of material from Inner Mongolia and Ningxia to the first author and to Prof. Masahiro Ohara (Sapporo) for the loan of the Watanabe types. The research was supported jointly by the Foundation for Key University Teachers by the Ministry of Education (No. 2011697505), the National Natural Science Foundation of China (NSFC, No. 31201732, 31572300), the foundation of Shaanxi Educational Committee (No. 11JK0614), the Research Fund for the Doctoral Program of Higher Education of China (No. 20116101120001), the National Science Foundation for Fostering Talents in Basic Research of NSFC (No. J12100063) and the Opening Foundation of Key Laboratory of Resource Biology and Biotechnology in western China (Northwest University), Ministry of Education.

References

  • Achterberg C van (1988) Revision of the subfamily Blacinae Foerster (Hymenoptera, Braconidae). Zoologische Verhandelingen Leiden 249: 1–324.
  • Achterberg C van (1993) Illustrated key to the subfamilies of the Braconidae (Hymenoptera: Ichneumonoidea). Zoologische Verhandelingen Leiden 283: 1–189.
  • Achterberg C van (2009) Can Townes type Malaise traps be improved? Some recent developments. Entomologische Berichten Amsterdam 69: 129–135.
  • Achterberg C van, Grootaert P, Shaw MR (2010) Chapter 17 – Flight interception traps for arthropods. In: Eymann J, Degreef J, Häuser C, Monje JC, Samyn Y, VandenSpiegel D (Eds) Manual on field recording techniques and protocols for All Taxa Biodiversity Inventories and Monitoring.Abc Taxa 1/2: 423–462.
  • Achterberg C van (2013) De Nederlandse Gasteruptiidae of Hongerwespen (Hymenoptera: Evanioidea). Nederlandse Faunistische Mededelingen 39: 55–87.
  • Achterberg C van, Talebi AA (2014) Review of Gasteruption Latreille (Hymenoptera, Gasteruptiidae) from Iran and Turkey, with the description of 15 new species. ZooKeys 458: 1–188. doi: 10.3897/zookeys.458.8531
  • Achterberg C van (in prep.) Revision of the East Palaearctic Gasteruption Latreille (Evanioidea: Gasteruptiidae: Gasteruptiinae).
  • Cameron P (1888) Descriptions of one new genus and some new species of parasitic Hymenoptera. Proceedings of the Manchester Literary and Philosophical Society 26: 117–137.
  • Crosskey RW (1951) The morphology, taxonomy and biology of the British Evanioidea (Hymenoptera). Transactions of the Royal Entomological Society of London 102: 247–301. doi: 10.1111/j.1365-2311.1951.tb00749.x
  • Gauld ID, Hanson PE (1995) The evaniomorph parasitoid families. Chapter 8. In: Hanson PE, Gauld ID (Eds) The Hymenoptera of Costa Rica. Oxford University Press, Oxford.
  • Hanson PE, Gauld ID (2006) Hymenoptera de la région neotropical. Memoirs of the American entomological Institute 77: 1–994. [Enlarged translation of: Hanson, P.E. & I.D. Gauld (eds), 1995. The Hymenoptera of Costa Rica: 1–893]
  • He JH (2004) Hymenopteran Insect Fauna of Zhejiang. Science Press, Beijing.
  • Houston TF (1987) A second contribution to the biology of Stenocolletes bees (Hymenoptera: Apoidea: Stenotritidae). Records of the Western Australian Museum 13: 189–201.
  • Jennings JT, Parslow B (2014) Gasteruption youngi sp. nov. (Hymenoptera: Evanioidea: Gasteruptiidae) from South Australia; an unusual species with trichoid sensilla on the ovipositor sheaths. Zootaxa 3872(1): 95–100. doi: 10.11646/zootaxa.3872.1
  • Jennings JT, Austin AD (1997a) Revision of the Australian endemic genus Hyptiogaster Kieffer (Hymenoptera: Gasteruptiidae), with descriptions of seven new species. Journal of Natural History 31: 1533–1562. doi: 10.1080/00222939700770821
  • Jennings JT, Austin AD (1997b) Revision of Aulacofoenus Kieffer (Hymenoptera: Gasteruptiidae), hyptiogastrine wasps with a restricted Gondwanic distribution. Invertebrate Taxonomy 11: 943–976. doi: 10.1071/IT97003
  • Jennings JT, Austin AD (2000) Higher-level phylogeny of the Aulacidae and Gasteruptiidae (Hymenoptera: Evanioidea). In: Austin AD, Dowton M (Eds) Hymenoptera: Evolution, Biodiversity and Biological Control. CSIRO Publishing, Melbourne, 154–164.
  • Jennings JT, Austin AD (2002) Systematics and distribution of world hyptiogastrine wasps (Hymenoptera: Gasteruptiidae). Invertebrate Systematics 16: 735–811. doi: 10.1071/IT01048
  • Jennings JT, Austin AD (2004) Biology and host relationships of aulacid and gasteruptiid wasps (Hymenoptera: Evanioidea): a review. In: Rajmohana K, Sudheer K, Girish Kumar P, Santhosh S (Eds) Perspectives on Biosystematics and Biodiversity. University of Calicut, Kerala, 187–215.
  • Johansson N, Achterberg C van (submitted) Revision of the Palaearctic Gasteruption assectator aggregate (Hymenoptera, Gasteruptiidae), with special reference to Sweden. ZooKeys.
  • Latreille PA (1796) Précis des caractères génériques des insectes, disposes dans un ordre naturel. Paris & Bordeaux, 201 pp.
  • Macedo ACC (2009) Generic classification for the Gasteruptiinae (Hymenoptera: Gasteruptiidae) based on a cladistic analysis, with the description of two new Neotropical genera and the revalidation of Plutofoenus Kieffer. Zootaxa 2075: 1–32.
  • Macedo ACC (2011) A revision of Gasteruption Latreille (Hymenoptera: Gasteruptiidae) in the Neotropical region. Zootaxa 3030: 1–62.
  • Malyshev SI (1965) Lebensweise und Instinkte der primitiven Schlupfwespen Gasteruptiidae (Hymenoptera). Zoologische Jahrbücher. Abteilung für Systematik, Okologie und Geographie der Tiere 92: 239–288.
  • Malyshev SI (1968) Genesis of the Hymenoptera and the Phases of their Evolution. Springer, 319 pp. doi: 10.1007/978-1-4684-7161-8
  • Pasteels JJ (1958) Révision du genre Gasteruption (Hymenoptera, Evanioidea, Gasteruptionidae). V. Espèces indomalaises. Bulletin et Annales de la Société Royale Entomologique de Belgique 94: 169–213.
  • Semenov A (1892) Revisio Hymenopterorum Musei Zoologici Academiae Caesareae Scientiarum Petropolitanae. III Familia Evaniidae. Bulletin de l’Académie Impériale des Sciences de St.-Pétersbourg, Nouvelle Serie 3, 35: 9–30.
  • Watanabe C (1934) On Evaniidae and Gasteruptionidae from Japan (Hymenoptera). Transactions of the Sapporo Natural History Society 13(3): 280–286.
  • Zhao K-x, Achterberg C van, Xu Z-f (2012) A revision of the Chinese Gasteruptiidae (Hymenoptera, Evanioidea). ZooKeys 237: 1–123. doi: 10.3897/zookeys.237.3956
  • Žikić V, Achterberg C van, Stanković SS, Dubaić JB, Četković A (2014) Review of the Gasteruptiidae (Hymenoptera: Evanioidea) from the territory of the former Yugoslavia, with three newly reported species. Zootaxa 3793(5): 573–586. doi: 10.11646/zootaxa.3793.5.5
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