identifier	taxonID	type	CVterm	format	language	title	description	additionalInformationURL	UsageTerms	rights	Owner	contributor	creator	bibliographicCitation
F62A8783203E4D3FFC589FC7FA89F783.text	F62A8783203E4D3FFC589FC7FA89F783.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Aptesis Forster 1850	<div><p>Genus Aptesis Förster, 1850</p> <p>Aptesis Förster, 1850: 71. Type species: Ichneumon sudeticus Gravenhorst, 1815. Designated by Viereck (1914).</p> <p>Pezoporus Förster, 1869: 181. Type species: Ichneumon nigrocinctus Gravenhorst, 1815. Name preoccupied.</p> <p>Clypediodon Aubert, 1968: 7. Type species: Aptesis (Clypeodiodon) flavifaciator Aubert, 1968. Original designation.</p> <p>Diagnosis. Townes (1970) proposed diagnosis of this genus. We refer it with some additional data of character states of Japanese species below. Clypeus weakly to moderately convex in lateral view, its apex truncate or somewhat arcuate (Figs 1B, 2B, 3A, B). Median 0.2 and more of apical margin of clypeus sharp, narrowly reflexed (Figs 1B, 2B, 3A, B). Mandible with two teeth, its upper tooth as long as (Fig. 3B) or shorter than lower tooth. Apical half of flagellum not strongly flattened below, not strongly tapered to apex (Figs 1A, 2A, 3A). Basal flageller segments short and slender (Figs 1A, 2A, 3A), F2 shorter than 3.3 times as long as wide in lateral view. Propodeal spiracle not strongly elongate (Fig. 3E), at most 2.0 times as long as wide. Areolet pentagonal (Fig. 3C). Spiracle of T1 situated behind the mid-length (Fig. 3D). Postpetiole usually with a complete or incomplete dorsolateral longitudinal carina or ridge between its spiracle and apicolateral corner (Fig. 3D). T2 more or less polished (Figs 1A, F, 2A). Ovipositor straight, its upper valve without oblique or transverse teeth (Figs 1A, 3F).</p> <p>Distribution. Holarctic, Oriental and Afrotropical regions (Yu et al., 2012).</p> <p>Remarks. Eleven species of this genus were previously recorded from Eastern Palaearctic region (Yu et al., 2012; Li et al., 2013). Japanese fauna of this genus is still poorly studied. We recognized seven species of this genus from Japan. Three of them are described species, A. albibasalis (Uchida, 1930), A. albidipes (Walker, 1874) and A. opaca (Cushman, 1937). In this study, we describe a new species, Aptesis flavitrochanterus sp. nov., which was previously recorded as Aptesis sp. A by Taniwaki &amp; Watanabe (2012). The remainders may be undescribed or unrecorded species.</p> <p>Females of Japanese species of this genus can be distinguished by the following preliminary key. Identification of males difficult, thus identification of the new species should be compared with the following original description.</p></div> 	https://treatment.plazi.org/id/F62A8783203E4D3FFC589FC7FA89F783	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Plazi	Watanabe, Kyohei;Taniwaki, Tooru	Watanabe, Kyohei, Taniwaki, Tooru (2018): Taxonomic Study of the Genera Förster, 1850, and Cameron, 1903 (Hymenoptera, Ichneumonidae, Cryptinae) associated with (Hymenoptera, Tenthredinidae), with Description of a New Species. Bulletin of the Kanagawa Prefectural Museum (Natural Science) 47: 73-84, DOI: 10.5281/zenodo.13222915
F62A8783203C4D38FE9E9A2BFEFAF8B3.text	F62A8783203C4D38FE9E9A2BFEFAF8B3.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Aptesis flavitrochanterus Watanabe & Taniwaki 2018	<div><p>Aptesis flavitrochanterus sp. nov.</p> <p>(Figs 1A–F, 2A–C, 3A–F)</p> <p>Aptesis sp. A Taniwaki &amp; Watanabe, 2012: 6.</p> <p>Type series. [Holotype] F, Kanagawa Pref., Kiyokawa Vil., Miyagase, Mt. Tanzawasan, Tennoji-one 1350 m alt., 24. XII. 2008 (coll. cocoon of Fagineura crenativora), 23. II. 2009 (em. from the cocoon), T. Taniwaki leg. (KPM-NK 5006655). [Paratypes] 1 M, same data of holotype except for 19. II. 2009 (em. from the cocoon) (KPM-NK 5006658); 2 M, same data of holotype except for 19. XI. 2008 (coll.), 16. II. 2009 (em. from the cocoon) (KPM-NK 5006659, 5006660); 1 F, same data of holotype except for 9. II. 2008 (coll.), 18. III. 2009 (em. from the cocoon) (KPM-NK 5006661); 1 F 2 M, same data of holotype except for 23. IV. 2008 (coll.), 4 (M), 18 (M), 24 (F). V. 2009 (em. from the cocoon) (KPM-NK 5006662–64); 1 F, same locality and collector of holotype, 16. III. 2009 (coll. cocoon of Fagineura crenativora), 19. IV. 2009 (em. from the cocoon), T. Taniwaki leg. (KPM-NK 5006665); 1 F, same locality and collector of holotype, 30. IV. 2009 (coll. cocoon of Fagineura crenativora), 3. V. 2009 (em. from the cocoon) (KPM-NK 5006666); 1 M, same locality and collector of holotype, 8. IV. 2009 (coll. cocoon of Fagineura crenativora), 3. V. 2009 (em. from the cocoon) (KPM-NK 5006666); 1 F, same locality and collector of holotype, 8. IV. 2009 (coll. cocoon of Fagineura crenativora), 8. V. 2009 (em. from the cocoon) (KPM-NK 5006669); 1 M, same locality and collector of holotype, 30. IV. 2009 (coll. cocoon of Fagineura crenativora), 20. V. 2009 (em. from the cocoon) (KPM-NK 5006670); 1 F, Kanagawa Pref., Kiyokawa Vil., Miyagase, Mt. Tanzawasan, Tennoji-one 1350 m alt., 16. V. 2013, T. Taniwaki leg. (FIT) (KPM-NK 5004398); 1 F, same locality and collector, 31. V. 2013 (KPM-NK 5004333); 2 F, same locality and collector, 15. VI. 2013 (KPM-NK 5004320, 5004327); 1 F, same locality and collector, 20. VI. 2013 (KPM-NK 5004321); 1 F, Kanagawa Pref., Kiyokawa Vil., Miyagase, Mt. Tanzawasan 1550 m alt., 9. V. 2013, T. Taniwaki leg. (FIT) (KPM-NK 5004319); 3 F, same locality and collector, 15. VI. 2013 (KPM-NK 5004324, 5004329, 5004423); 2 F, same locality and collector, 20. VI. 2013 (KPM-NK 5004328, 5004330); 1 F, same locality and collector, 4. VII. 2013 (KPM-NK 5004323); 1 M, Kanagawa Pref., Yamakita Town, Kurokura, Mt. Hinokiboramaru 1550 m alt., 6. II. 2008 (coll. cocoon of Fagineura crenativora), 11. III. 2009 (em. from the cocoon), T. Taniwaki leg. (KPM-NK 5006671); 1 F, same locality, 21. V. 2013, T. Taniwaki leg. (FIT) (KPM-NK 5004332); 1 F, same locality and collector, 28. VI. 2013 (KPM-NK 5004322); 1 F, same locality and collector, 6. VII. 2013 (KPM-NK 5004331); 1 F, Kanagawa Pref., Yamakita Town, Nakagawa, Mt. Komotsurushiyama 1350 m alt., 21. VI. 2013, Taniwaki leg. (FIT) (KPM-NK 5004325); 1 F, Kanagawa Pref., Yamakita Town, Yoduku, Mt. Mikuniyama 1350 m alt., 21. VI. 2013, Taniwaki leg. (FIT) (KPM-NK 5004326); 1 F, same locality and collector, 4. VII. 2013 (KPM-NK 5004385); 1 F, Yamanashi Pref., Koushu City, Mt. Daibosatsu, Kaminikkawa-toge, 16. VI. 2007, H. Katahira leg. (KPM-NK 5006673); 1 F, Nagano Pref., Outaki Vil., Mt. Ontakesan, Tanohara 1800 m alt., 8. VIII. 2007, K. Watanabe leg. (KPM-NK 5006674).</p> <p>Description. Female (n = 25). Body length 3.5–5.5 (HT: 5.3) mm. Body polished, smooth and punctate, covered with silver setae.</p> <p>Head 0.6–0.65 (HT: 0.65) times as long as wide. Clypeus 0.45–0.5 (HT: 0.45) times as long as wide, punctures on ventral area sparser than dorsal area (Fig. 1B). Face 0.4 times as long as wide, weakly convex medially, interspace of punctures mat (Fig. 1B). OOL 0.9–2.0 (usually 1.0, HT: 1.0) times as long as POL. Occipital carina complete, its lower end connected with hypostomal carina distant from base of mandible. MSL 1.2–1.4 (HT: 1.2) times as long as BWM. Subocular sulcus absent. Malar space with a distinct mat area. Antenna with 19–21 (HT: 20) flagellomeres. F1 1.0–1.05 (HT: 1.05) times as long as F2. F2 1.7–2.0 (HT: 2.0) times as long as maximum depth in lateral view.</p> <p>Mesosoma. Pronotum punctate, obliquely or longitudinally striated ventrally (Fig. 3A). Epomia present but weak (Fig. 3A). Mesonotum punctate, punctures on median part larger than other areas, with distinct, short notauli (Figs 1C, 3A). Mesopleuron without a large smooth area around episternal scrobe, its punctures partly longitudinally or obliquely confluent each other. Upper end of epicnemial carina not reached to anterior margin of mesopleuron (Fig. 3A). Subalar prominence convex. Lower division of metapleuron with a juxtacoxal carina, its posterior end sometimes indistinct. Lateromedian longitudinal carinae and anterior transverse carina of propodeum absent or partly indistinctly present (Fig. 3E). Posterior transverse carina of propodeum and pleural carinae complete (Fig. 3E). Areas along posterior transverse carina of propodeum usually some longitudinal or irregular rugae (Fig. 3E). Propodeal apophysis developed but weak (Fig. 1A). Fore wing 3.6–4.8 (HT: 4.1) mm, without a ramulus. Anterior end of vein cu-a of fore wing opposite or almost opposite to posterior end of vein Rs+M. Lateral sides of areolet convergent anteriorly (Fig. 3C). Vein 1-cu of hind wing more than 6.0 times as long as vein cu-a of hind wing. Hind femur 3.8–4.1 (HT: 4.1) times as long as maximum depth in lateral view. Tarsal claws simple.</p> <p>Metasoma. T1 1.4–1.85 (HT: 1.85) times as long as maximum width, largely smooth, without median dorsal carinae, with dorsolateral carinae except for apex (Figs 1F, 3D, E). T2 1.1–1.4 (HT: 1.3) times as long as maximum width. T2 and T3 covered with fine punctures except for median large smooth area (Fig. 1F). T4–T7 finely and sparsely punctate. Ovipositor sheath longer than T1 and 0.9–1.0 (HT: 1.0) times as long as hind tibia, its base sometimes concealed under tergites and thus measurement difficult in this case. Apex of ovipositor as Fig. 3F.</p> <p>Colouration (Figs 1 A-F). Body (excluding wings and legs) black to blackish brown, except for: palpi dark brown, flagellum with a white band (usually present on F6–F10) and a ventral reddish-brown surface on apical segments, mandible and clypeus more or less partly tinged with reddish-brown, inner orbit sometimes with a pair of reddish-brown markings along antennal sockets, tegula sometimes tinged with brown, T2–T7 sometimes tinged with brown, and ovipositor reddish-brown. Wings hyaline, with dark brown to blackish-brown veins and pterostigma except for yellow wing base. Legs black to blackish brown, except for: trochanters and trochanteli white to whitish-yellow (sometimes more or less darkened), fore and mid tibiae and tarsi largely yellowish-brown, apex and base of femora narrowly tinged with yellowish-brown, coxae and basal part of hind tibia sometimes tinged with yellowish-brown.</p> <p>Male (n = 9). Similar to female. Body length 5.5–7.1 mm. Clypeus 0.4–0.5 times as long as wide. Face 0.45–0.5 times as long as wide. OOL 1.3–1.8 times as long as POL. MSL 0.6–0.7 times as long as BWM. Antenna with 25–27 flagellomeres. F2 2.0–2.2 times as long as maximum depth in lateral view, with tyloids on F11-14 (sometimes also F10 and F15) (Fig. 2C). Fore wing 4.7–5.8 mm. Hind femur 4.4–4.5 times as long as maximum width in lateral view. T1 2.35–2.8 times as long as maximum width. T2 0.75–1.2 times as long as maximum width. T2–T7 entirely covered with punctures. Apex of paramere beyond the apex of aedeagus. Face whitish yellow except for a small median black area below antennal sockets (Fig. 2B). Antenna without a white band and usually without a ventral reddish-brown area (Fig. 2A). Clypeus, malar space, ventral surface of scape, and apex of pedicel whitish yellow (Fig. 2B). Tegula tinged with whitish-yellow laterally (Fig. 2A). Thyridium and posterior margin of T2 reddish-brown. Fore and mid legs usually paler than female (Fig. 2A).</p> <p>Egg. White, elongate, its length ca. 1.0 mm (Taniwaki &amp; Watanabe, 2014).</p> <p>Distribution. Japan (Honshu).</p> <p>Etymology. The specific name is from the white trochanter of hind leg.</p> <p>Bionomics. Host is Fagineura crenativora (common species of parasitoid complex of the sawfly) (Taniwaki &amp; Watanabe, 2012, 2014). Adult emerged from host cocoon (Taniwaki &amp; Watanabe, 2012, 2014). The ovipositor behaviour was reported by Taniwaki &amp; Watanabe, i.e., 1) adult female initially dug into the soil to search for cocoons of their host, 2) on the detection of cocoons, they laid their eggs inside the cocoon, 3) the eggs can be easily dropped from the body of host inside cocoons.</p> <p>Remarks. This species resembles A. melana and A. opaca, but its females can be distinguished by the following combination of character states: hind trochanter and trochantellus largely white to yellow (black to brown in A. melana and A. opaca); T1 1.4–1.85 times as long as maximum width (1.3 times in A. melana); body length 3.5–5.5 mm (8.5–10.0 mm in A. opaca); ovipositor sheath longer than T1 and 0.9–1.0 times as long as hind tibia (shorter than T 1 in A. opaca and 0.8 times as long as hind tibia in A. melana). The males of this species can be distinguished from other Japanese species and A. melana by the following combination of characters: face entirely yellow to white except for median dorsal area (black in A. albibasalis); clypeus entirely yellow to white; tyloids of antenna present on F10–F15 (F 13–19 in A. albibasalis); hind tarsus blackish-brown to black (with a yellowish-brown to white area in A. opaca, A. albidipes and A. melana).</p> </div>	https://treatment.plazi.org/id/F62A8783203C4D38FE9E9A2BFEFAF8B3	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Plazi	Watanabe, Kyohei;Taniwaki, Tooru	Watanabe, Kyohei, Taniwaki, Tooru (2018): Taxonomic Study of the Genera Förster, 1850, and Cameron, 1903 (Hymenoptera, Ichneumonidae, Cryptinae) associated with (Hymenoptera, Tenthredinidae), with Description of a New Species. Bulletin of the Kanagawa Prefectural Museum (Natural Science) 47: 73-84, DOI: 10.5281/zenodo.13222915
F62A878320394D38FEC49849FCE0F783.text	F62A878320394D38FEC49849FCE0F783.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Javra Cameron 1903	<div><p>Genus Javra Cameron, 1903</p> <p>parviceps Cameron, 1903). Monobasic.</p> <p>Finchra Cameron, 1907: 463. Type species: Finchra gracilis Cameron, 1907. Monobasic.</p> <p>Monocryptus Hellén, 1957 (“1956”): 135. Type species: Cratocryptus opacus Thomson, 1873. Monobasic.</p> <p>Diagnosis. Townes (1970) proposed diagnosis of this genus. We refer it with some additional data of character states of Japanese species below. Mandible with two teeth, its upper tooth as long as or shorter than lower tooth. Flagellum slender (Figs 4A, 5A), F2 3.0–5.5 (female) or 2.7–4.0 (male) times as long as depth in lateral view. Apical half of flagellum not strongly flattened below, not strongly tapered to apex (Figs 4A, 5A). Propodeal spiracle not strongly elongate (Fig. 5D), at most 2.0 times as long as wide. Areolet pentagonal, rectangular, or quadrangular. T2 mat (Fig. 4C). Spiracle of T1 situated behind the mid-length (Fig. 5C). Ovipositor straight, its upper valve without oblique or transverse teeth (Fig. 5E). Clypeus ca. 0.5 times as long as wide in male.</p> <p>Distribution. Holarctic and Oriental regions (Yu et al., 2012).</p> <p>Remarks. Two species, J. coreensis and J. teranishii (Uchida, 1952), were previously recorded from Eastern Palaearctic region (Yu et al., 2012). Japanese fauna of this genus is still poorly studied. We recognized eight species of this genus from Japan. Three of them are described species, J. coreensis, J. taniguchiae (Uchida, 1956), and J. teranishii. In this study, we record J. coreensis from Japan for the first time, which was previously recorded as female of Javra sp. by Taniwaki &amp; Watanabe (2012). The remainders may be undescribed or unrecorded species. Japanese species of this genus can be identified by the following key.</p> <p>Javra Cameron, 1903: 47. Type species: Javra parviceps Cameron, 1903. Monobasic.</p> <p>Cnemocryptus Cameron, 1903: 38. Type species: Cnemocryptus validicornis Cameron, 1903 (= J avra</p> </div>	https://treatment.plazi.org/id/F62A878320394D38FEC49849FCE0F783	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Plazi	Watanabe, Kyohei;Taniwaki, Tooru	Watanabe, Kyohei, Taniwaki, Tooru (2018): Taxonomic Study of the Genera Förster, 1850, and Cameron, 1903 (Hymenoptera, Ichneumonidae, Cryptinae) associated with (Hymenoptera, Tenthredinidae), with Description of a New Species. Bulletin of the Kanagawa Prefectural Museum (Natural Science) 47: 73-84, DOI: 10.5281/zenodo.13222915
F62A878320374D37FED69B20FA80F951.text	F62A878320374D37FED69B20FA80F951.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Javra coreensis (Uchida 1930)	<div><p>Javra coreensis (Uchida, 1930)</p> <p>(Figs 4A–C, 5A–E)</p> <p>Acanthocryptus coreensis Uchida, 1930: 330.</p> <p>Javra sp. Taniwaki &amp; Watanabe, 2012: 6. In part (female), misident.</p> <p>Description. Female (n = 35). Body 5.0– 7.5 mm. Body polished, mat, covered with silver setae.</p> <p>Head 0.6 times as long as wide. Clypeus 0.4–0.5 times as long as wide, weakly convex in lateral view (Fig. 5A), covered with large, sparse punctures dorsally, smooth ventrally. Face 0.4–0.45 times as long as wide, weakly convex in lateral view (Fig. 5A), punctate. Frons weakly concave, punctate except for smooth area above each antennal socket. OOL 1.0–1.2 times as long as POL. Occipital carina complete, its lower end connected with hypostomal carina distant from base of mandible. MSL 1.2–1.3 times as long as BWM. Antenna with 22–24 flagellomeres, F1 1.2–1.3 times as long as F2. F2 3.8–4.5 times as long as maximum depth in lateral view.</p> <p>Mesosoma. Pronotum without epomia. Mesonotum with notauli anteriorly. Scutellum weakly convex, covered with sparse punctures. Mesopleuron covered with irregular to longitudinal rugae, without a smooth area around episternal scrobe. Upper end of epicnemial carina closed to anterior margin of mesopleuron. Subalar prominence convex. Lower division of metapleuron with a complete juxtacoxal carina. Propodeal carinae complete or sometimes lateral section of anterior transverse carina and median section of lateral longitudinal carinae partly indistinct (Fig. 5D). Propodeal apophysis well developed (Fig. 4A). Fore wing 5.5–7.0 mm. Anterior end of vein cu-a of fore wing opposite or slightly distad from posterior end of vein Rs+M. Lateral sides of areolet parallel (Fig. 5B) or weakly convergent anteriorly. Vein 1-cu of hind wing more than 6.0 times as long as vein cu-a of hind wing. Legs covered with gold setae. Hind femur 5.7–6.3 times as long as maximum depth in lateral view. Tarsal claws simple.</p> <p>Metasoma. T1 2.05–2.35 (usually 2.1–2.2) times as long as maximum width, with median dorsal carinae except for postpetiole, with dorsolateral carinae except for apex (Fig. 5D). T2 0.65–0.75 times as long as maximum width. Ovipositor sheath 0.7–0.8 times as long as hind tibia. Apex of ovipositor as Fig. 5E, basal two teeth longer than apical teeth.</p> <p>Colouration (Figs 4A–C). Body (excluding wings) black to blackish brown, except for: white band of flagellum (usually F5–F9); ventral surface of apical part of flagellum usually with a large reddish-brown area; mandible partly tinged with yellowish-brown; fore tibial spur yellowish-brown; base and apex of all legs and base of all tibiae more or less tinged with reddish-brown to yellowish-brown; posterior margin of each metasomal tergites sometimes narrowly tinged with reddish-brown; ovipositor reddish-brown. Wings hyaline, with dark brown to blackish-brown veins and pterostigma except for yellow wing base.</p> <p>Male. Unknown.</p> <p>Materials examined. JAPAN: 1 F, Kanagawa Pref., Kiyokawa Vil., Miyagase, Mt. Tanzawasan, Tennoji-one 1350 m alt., 8. IV. 2009 (coll. cocoon of Fagineura crenativora), 1. V. 2009 (em. from the cocoon), T. Taniwaki leg. (KPM-NK 5006654); 1 F, same locality and collector, 15. VI. 2013 (FIT) (KPM-NK 5004376); 3 F, same locality and collector, 20. VI. 2013 (KPM-NK 5004356, 5004358, 5004377); 1 F, same locality and collector, 29. VI. 2013 (KPM-NK 5004365); 3 F, Kanagawa Pref., Kiyokawa Vil., Miyagase, Mt. Tanzawasan 1550 m alt., 20. VI. 2013, T. Taniwaki leg. (FIT) (KPM-NK 5004361, 5004380, 5004382); 4 F, same locality and collector, 29. VI. 2013 (KPM-NK 5004357, 5004360, 5004364, 5004381); 3 F, same locality and collector, 29. VI. 2013 (KPM-NK 5004359, 5004373, 5004375); 6 F, Kanagawa Pref., Yamakita Town, Kurokura, Mt. Hinokiboramaru 1550 m alt., 23. V. 2013, T. Taniwaki leg. (FIT) (KPM-NK 5004353–54, 5004367, 5004370, 5004372, 5004374); 1 F, same locality and collector, 14. VI. 2013 (KPM-NK 5004369); 2 F, same locality and collector, 23. VI. 2013 (NIAES); 2 F, same locality and collector, 28. VI. 2013 (KPM-NK 5004366, 5004368); 6 F, same locality and collector, 6. VII. 2013 (KPM-NK 5004350–52, 5004362–63, 5004371). KOREA: 1 F (lectotype), Sambo, 29. VII. 1922, T. Uchida leg. (SEHU).</p> <p>Distribution. Japan (Honshu) and Korea.</p> <p>Bionomics. Host is Fagineura crenativora (rare species in the parasitoid complex of the sawfly) (Taniwaki &amp; Watanabe, 2012). Adult emerged from host cocoon (Taniwaki &amp; Watanabe, 2012).</p> <p>Remarks. This is the first record from Japan. F. crenativora is also the first host record of this species.</p> </div>	https://treatment.plazi.org/id/F62A878320374D37FED69B20FA80F951	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Plazi	Watanabe, Kyohei;Taniwaki, Tooru	Watanabe, Kyohei, Taniwaki, Tooru (2018): Taxonomic Study of the Genera Förster, 1850, and Cameron, 1903 (Hymenoptera, Ichneumonidae, Cryptinae) associated with (Hymenoptera, Tenthredinidae), with Description of a New Species. Bulletin of the Kanagawa Prefectural Museum (Natural Science) 47: 73-84, DOI: 10.5281/zenodo.13222915
