Stenocranus harimensis Matsumura, 1935

Fujinuma, Satoshi & Hayashi, Masami, 2025, Taxonomic revision of Japanese Stenocranus (Hemiptera: Fulgoromorpha: Delphacidae), Zootaxa 5706 (3), pp. 301-336 : 318-320

publication ID

https://doi.org/10.11646/zootaxa.5706.3.1

publication LSID

lsid:zoobank.org:pub:8EC89B9A-3A22-4437-AE42-DF61387992EC

DOI

https://doi.org/10.5281/zenodo.17881104

persistent identifier

https://treatment.plazi.org/id/F1704704-D645-AD3E-FF1A-FC08FBEC8EFB

treatment provided by

Plazi

scientific name

Stenocranus harimensis Matsumura, 1935
status

 

Stenocranus harimensis Matsumura, 1935 View in CoL

[Japanese name: Harima-naga-unka (Hoso-naga-unka)]

( Figs 1 View FIGURE 1 , 4 View FIGURE 4 , 9 View FIGURE 9 , 10 View FIGURE 10 , 12 View FIGURE 12 , 15 View FIGURE 15 )

Stenocranus harimensis Matsumura, 1935: 129 View in CoL [ Type locality: Japan ( Honshu : Tansanji ( Taisanji ), near Akashi in the Prov. Harima; Chichibu, Abiko)].

Stenocranus elongatus Matsumura, 1935: 127 View in CoL [ Type locality: Japan ( Honshu !: Buzen ( Jono)]. syn. nov.

Lectotype designation. Four male syntypes (abdomen lost in two) are preserved in the Matsumura collection, with a red label on the same pin; thus, one male is designated as the lectotype. Some other specimens labeled as S. harimensis View in CoL from the same locality are identified as S. takasagonis Matsumura. View in CoL

Type material examined. Lectotype ♂ (here designated; SEHU), “28/VI Japan [ Taisanji (in Japanese)] Dr Matsumura // (red label) harimensis n.” . Paralectotypes: 3♂ ( SEHU), same data as lectotype . Holotype ♀ of S. elongatus (SEHU) , “ Japan Yano [Buzen (in Japanese)] Matsumura // elongatus M. det. Dr. Matsumura // (red label) elongatus Type” .

Other material examined. [Honshu] 5♂ 5♀ ( SF), Kamitakamori, Tsukidate, Kurihara , Miyagi Pref., 29. X. 2022, S. Fujinuma ; 5♂ 5♀ ( SF), Watarase Marsh, Fujioka , Tochigi, Tochigi Pref., 4. V. 2011, S. Fujinuma ; 2♂ 3♀ ( MH), Hozoji swamp, Mitakaya, Hanyu , Saitama Pref., 15. X. 2012, M. Hayashi et al .; 3♂ ( SF), same data except 25. IX. 2016, S. Fujinuma ; 11♂ 4♀ ( MH), Kurohama, Hasuda , Saitama Pref., 6. VIII. 1999 ( light trap), S. Ishida ; 8♂ ( MH), Heirinji, Iwatsuki , Saitama Pref., 8. VIII. 1999, S. Ishida ; 1♂ ( MH), Murakuni, Iwatsuki , Saitama Pref., 15. VII. 1999 ( light trap), S. Ishida ; 1♂ 2♀ ( MH), Akigase, Urawa , Saitama Pref., 31. I. 1987, M. Hayashi et al .; 3♂ ( MH), same data except 20. VI. 1990 ( light trap) ; 8♂ 15♀ ( SF), Kitaokawara, Minamiyamashiro , Kyoto Pref., 19. VI. 2015, S. Fujinuma; [ Tsushima Is.] 1♂ 1♀ ( MH), Meboro, Kami-agata , 27. X. 2002, M. Hayashi et al .; 1♂ ( MH), Mt. Ôboshi, Mine , 26. X. 2002, M. Hayashi et al .; 3♀ ( MH), Sumo, Mitsushima , 26. V. 1999, M. Hayashi et al.; [ Minami-Daito Is.] 2♀ ( MH), Ikenosawa , 18. IV. 1998, M. Hayashi .

Redescription. General coloration brown, strongly darker in summer form. Frons and genae mostly darker, carinae paler. Mid-dorsal parts of vertex, pronotum, and mesonotum widely whitish, fringed with orange and dark stripes (orange stripes usually lacking in summer form). Forewings translucent, brownish; veins darker particularly in membrane; dark markings on apices of apical veins; dark stripes along MP 3+4, the stripes broadly expanded in summer form. Male pygofer pale to dark brown.

Vertex about 1.5× as long as wide. Frons about 2.6× as long as wide, with median carina forked in apical 1/3 (rarely with two median carinae). Antennal segment II about 2.4× as long as wide. Forewing venation and hind leg spinulation as in S. niisimai . Post-tibial spur with 13–16 fine teeth.

Body length (mean): ♂ 4.7–5.8 mm ( 5.4 mm); ♀ 5.6–6.5 mm (6.0 mm).

Male genitalia: Similar to S. sapporensis except pygofer blunter at lateral sides of opening for gonostyles; apical process of phallotheca with short process on its base and minute process on subapex. Female genitalia is also similar to S. sapporensis except gonapophyses IX with 18–21 teeth; gonoplacs much rounded and wider in apical half.

Distribution. Japan ( Hokkaido, Honshu, Shikoku, Kyushu, Tsushima Is., Minami-Daito Is.).

Remarks. This species is similar to S. sapporensis in having the dark body and frons rarely with two median carinae, but it can be distinguished by the absence of curved stripes on the forewings and by the presence of a minute subapical process on the phallotheca. Examination of the holotype of Stenocranus elongatus Matsumura from Japan revealed that its habitus and female genital structures are identical to those of S. harimensis . Although S. elongatus has page precedence over S. harimensis , it was described based on a single female specimen, whereas S. harimensis was described based on male and female specimens. Therefore, it is preferable that S. elongatus becomes a junior synonym of S. harimensis for stability and universality of nomenclature (ICZN 4th edition: Recommendation 24A). In the original description of S. elongatus , the distribution is erroneously noted as Honshu; the type locality is actually “Jono in the Prov. Buzen,” northern Kyushu, western Japan.

Biological notes. This species inhabits mountainous to lowland marshes and feeds on Cyperus serotinus Rottb. ( Kisimoto 1995), Schoenoplectus triqueter (L.), and Carex dispalata Boott ( Cyperaceae ). Females lay eggs exclusively in the middle to upper parts of scapes of C. dispalata in spring but shift oviposition sites to the lower parts of leaves in summer, as observed in some congeners feeding on the same host.

SF

Universidad Nacional del Litoral

MH

Naturhistorisches Museum, Basel

Kingdom

Animalia

Phylum

Arthropoda

Class

Insecta

Order

Hemiptera

Family

Delphacidae

Genus

Stenocranus

Loc

Stenocranus harimensis Matsumura, 1935

Fujinuma, Satoshi & Hayashi, Masami 2025
2025
Loc

Stenocranus harimensis

Matsumura 1935: 129
1935
Loc

Stenocranus elongatus

Matsumura 1935: 127
1935
Loc

S. harimensis

Matsumura 1935
1935
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