Stephanitis (Norba) exigua Horvath , 1912

Souma, Jun, 2022, Integrative taxonomy of the Lauraceae - feeding species of the genus Stephanitis (Hemiptera, Heteroptera, Tingidae) from Japan, Deutsche Entomologische Zeitschrift 69 (2), pp. 219-281 : 219

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https://dx.doi.org/10.3897/dez.69.89864

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scientific name

Stephanitis (Norba) exigua Horvath , 1912
status

 

Stephanitis (Norba) exigua Horvath, 1912

[Japanese name: Himetabu-gunbai] Figs 2C View Figure 2 , 4C View Figure 4 , 7C View Figure 7 , 9C View Figure 9 , 11C View Figure 11 , 13C View Figure 13 , 15C View Figure 15 , 17C View Figure 17 , 19C View Figure 19 , 21C View Figure 21 , 23C View Figure 23 , 25C View Figure 25 , 27C View Figure 27 , 29C View Figure 29 , 31C View Figure 31 , 35 View Figure 35 , 40H, I View Figure 40

Stephanitis (Norba) exigua Horváth, 1912: 336. Syntype(s) (Fig. 34C View Figure 34 ): Japan: Okinawa [= Ryukyu Islands, Okinawa-ken (an administrative area including a number of islands) or Okinawa Island (an island)] and Tateyama [= Honshu, Chiba-ken, Tateyama-shi, former Tateyama-machi in early 20th century (current Tateyama, Kamisanagura and Shimosanagura)]; ELHU and HNHM.

Stephanitis (Norba) aperta Horváth, 1912: Azuma and Kinjo (1987: 34) (distribution). Misidentification.

References.

Drake (1937: 594) (distribution); Drake (1948: 55) (checklist: Stephanitis ); Takeya (1951b: 13) (checklist: Japan); Drake and Maa (1953: 100) (checklist: Stephanitis ); Takeya (1953: 168) (distribution: part); Takeya (1963: 38) (distribution: part); Drake and Ruhoff (1965: 367) (catalog); Miyamoto (1964a: 274) (distribution: part); Miyamoto (1964b: 524) (distribution: part); Lee (1969: 246) (male genitalia); Jing (1981: 348) (monograph); Miyamoto and Yasunaga (1989: 168) (checklist: Japan); Tomokuni (1994: 843) (type material); Péricart and Golub (1996: 58) (catalogue: Palaearctic; Yamada and Tomokuni (2012: 204) (monograph: part); Yamada and Ishikawa (2016: 433) (checklist: Japan); Nakatani (2021: 78) (distribution).

Material examined.

Syntype (1 ♀, ELHU) (Fig. 34C View Figure 34 ), JAPAN: Honshu: “タテヤマ” [= Chiba-ken, Tateyama-shi, former Tateyama-machi in early 20th century (current Tateyama, Kamisanagura and Shimosanagura; approximate coordinates: 34°58'50.9"N, 139°51'27.1"E)], 11/VIII 1905 [= 11.viii.1905], “Matsumra” [sic; = collected by Shonen Matsumura and/or deposited in Matsumura’s collection]. As pointed out in a previous study ( Tomokuni 1994), this single female syntype corresponds to Stephanitis (Stephanitis) pyrioides (Scott, 1874) and does not match the original description of S. (Norba) exigua ( Horváth 1912). Therefore , if the remaining syntypes are present in ELHU and/or HNHM, a lectotype should be designated. Nevertheless , the former curator of HNHM does not know if the syntype of S. (N.) exigua exists in the collection (D. Rédei, pers. comm. 2021). Suspected syntypes (2 ♂♂ 1 ♀ 1 nymph, ELHU) (Fig. 35 View Figure 35 ), JAPAN: Ryukyu Islands : “Okinawa” [= Okinawa-ken (a prefecture including a number of islands) or Okinawa Island (an island)], "6 29". These four individuals were labelled with inscriptions of " Stephanitis yaeyamae " (unpublished name) and “Matsum” (collected by Shonen Matsumura and/or deposited in Matsumura’s collection). The species epithet of the unpublished name seems to refer to the Yaeyama Islands , the southern part of the Ryukyu Islands , but this morphological species is only distributed in the Daito Islands and the central part of the Ryukyu Islands . The morphological characteristics and locality data of three adult specimens match the original description of S. (N.) exigua ( Horváth 1912). However , the collector data of the four specimens are unclear and syntype (s) from “Okinawa” was (were) collected by “Kuroiwa” ( Horváth 1912). Therefore , these three adults could correspond to syntypes of S. (N.) exigua . In the present study, the author identified S. (N.) exigua based on three adult individuals. Non-types (106 ♂♂ 189 ♀♀ 7 nymphs), JAPAN: Ryukyu Islands (central part): Okinawa Island: 10.viii.1957, leg. T. Takara (1 ♀, NSMT); Kin, 14.vi.1958, leg. T. Takara (2 ♀♀, NSMT); Osato, 8.xi.1960, leg. K. Yasumatsu (2 ♂♂ 1 ♀, ELKU; 3 ♀♀, KUM); Yona, 14.xi.1960, leg. K. Yasumatsu (1 ♂, KUM); as above but 19.xi.1963, leg. H. Hasegawa (1 ♀, KUM); as above but 24.iii.1964, leg. Y. Miyatake (1 ♀, KUM); as above but 23.xi.1985, leg. M. Hayashi (2 ♂♂ 1 ♀, TUA); as above but 28.vi.1984, leg. M. Tomokuni (2 ♀♀, NSMT); Shuri, 2.vi.1961, leg. O. Nakoshi (1 ♂, KUM); Nago, 22.x.1963, leg. S. Uéno (1 ♂, KUM); Tamagusuku, 17.xi.1963, leg. H. Hasegawa (1 ♀, KUM); Kudeken, 20.iii.1964, leg. Y. Miyatake (2 ♂♂ 4 ♀♀, KUM); Izumi, 22.iii.1964, leg. T. Shirozu (9 ♂♂ 24 ♀♀, KUM); Izumi-Gogayama, 22.iii.1964, leg. S. Kimoto (1 ♂, KUM); as above but leg. Y. Miyatake (3 ♂♂ 2 ♀♀, KUM); Shoshi, 23.iii.1964, leg. S. Kimoto (1 ♂ 1 ♀, KUM); Nago, 23.iii.1964, leg. Y. Miyatake (1 ♂ 2 ♀♀, KUM); Hiji-Yonahadake, 25.iii.1964, leg. T. Shirozu (2 ♀♀, KUM); Hiji-gawa, 26.iii.1964, leg. T. Shirozu (1 ♀, KUM); Chinen, Sefa utaki, 17.ii.1973, leg. H. Hasegawa (1 ♀, NIAES); Yona, 21.ii.1973, leg. H. Hasegawa (1 ♀, NIAES); Kunigami-son, Mt. Yonahadake , 29.vi.1984, leg. M. Tomokuni (3 ♀♀, NSMT); Hanejiokawa, 14.xi.1985, leg. M. Hayashi (1 ♂ 2 ♀♀, TUA); Kunigami, Mt. Nishime , 19.x.1987, leg. M. Tomokuni (1 ♀, NSMT); Kunigami, Hama, 20.x.1987, leg. M. Sakai (1 ♂ 3 ♀♀, NSMT); Kunigami, Ooguni-rindo, 8 km from Yona, alt. 300 m, 21.x.1987, leg. M. Tomokuni (3 ♂♂ 3 ♀♀, NSMT); Kunigami, Hiji-Hiji Fall, 22.x.1987, leg. M. Tomokuni (1 ♂, NSMT); Kudeken, Seifa-utaki, 8.x.1988, leg. M. Sakai (1 ♂ 1 ♀, NSMT); Kunigamison, 10-11.x.1988, leg. K. Konishi (1 ♀, NIAES); Nago City, 12.x.1988, leg. K. Konishi (1 ♀, NIAES); Nakijin, Uebaru, 23.x.1990, leg. M. Hayashi et al. (1 ♂, NSMT); Afuso, 3.iv.1991, leg. M. Hayashi (1 ♂, TUA); Mt. Terukubi , 5.v.1991, leg. M. Hayashi (1 ♀, TUA); Mt. Yonahadake , 3.iv.1999, leg. M. Hayashi (1 ♀, TUA); Hedo, 16.ix.2002, leg. M. Hayashi (1 ♀, TUA); Kisebaru, 10.xii.2010, leg. M. Hayashi (1 ♀, TUA); Manzamô, 30.iii.2013, leg. M. Hayashi (1 ♂, TUA); Nago, Katsuyama, Mt. Katsuudake , 9.vi.2015, leg. H. Yoshitake (1 ♀, NIAES); Motobu, Namizato, Yaedake-sakura-no-mori-kôen, 30.iii.2018, leg. H. Yoshitake (4 ♂♂ 4 ♀♀, NIAES); Kunigami-son, Uka-rindô, 10.xi.2018, leg. H. Yoshitake (1 ♀, NIAES); Naha-shi, Shuri-sueyoshi-chô, Sueyoshi-kôen, 5.i.2019, leg. H. Yoshitake (1 ♀, NIAES); Yaese Park, 19.i.2019, leg. H. Shigetoh (4 ♂♂ 7 ♀♀ 1 nymph, TUA); as above but leg. H. Yoshitake (2 ♂♂ 1 ♀, NIAES); Nago-shi, Tanodake, 28.iv.2019, leg. R. Ito (1 ♂, TUA); Kunigami-gun, Kunigami-son, Sate, 6.v.2019, leg. R. Ito (1 ♂ 1 ♀, TUA); Nago, Genka Shisen For. Rd. , 3.vi.2019, leg. T. Saeki (1 ♂ 1 ♀, TUA); Uruma-shi, Mt. Ishikawadake , 29.xii.2019, leg. H. Shigetoh (2 ♂♂ 1 ♀, TUA); Naha-shi, Ohnoyama Park, 8.iii.2020, leg. J. Souma (4 ♂♂ 5 ♀♀ 3 nymphs); Kunigami-son, Aha, 5.v.2019, leg. H. Yoshitake (1 ♀, NIAES); as above but 18.iv.2020 (1 ♂ 1 ♀, NIAES); as above but 18.iv.2020, leg. H. Shigetoh (3 ♀♀, TUA); Toyomigusuku, 6.xi.2020, leg. J. Souma (1 ♀, TUA); Tabaru, 6.xi.2020, leg. J. Souma (1 ♂ 9 ♀♀, TUA); Midorigaoka Park, 10.xi.2020, leg. J. Souma (5 ♂♂ 4 ♀♀ 1 nymph, TUA); Nanjô-shi, Chinen-jôseki, 30.i.2021, leg. H. Yoshitake (1 ♀, NIAES); Kitanakagusuku-son, Taguchi, 3.ii.2021, leg. H. Yoshitake (1 ♀, NIAES); Nakagusuku, Noborimata, 3.ii.2021, leg. H. Yoshitake (1 ♀, NIAES); Okinawa-shi, Yaeshima-kôen, 4.ii.2021, leg. H. Yoshitake (1 ♀, NIAES); Uruma-shi, Enobi, 4.ii.2021, leg. H. Yoshitake (1 ♀, NIAES); Yomitan-son, Zakimi-jôseki, 5.ii.2021, leg. H. Yoshitake (1 ♀, NIAES); Yonabaru-chô, Untamamori, 20.ii.2021, leg. H. Yoshitake (1 ♀, NIAES); Nago-shi, Makiya, 1-2.vi.2021, leg. T. Saeki (1 ♀, TUA). Aka Island : 13.viii.1977, leg. M. Kinjo (1 ♀, NSMT); as above but 14.viii.1977 (1 ♀, NSMT); as above but 14.viii.1977, leg. S. Azuma (2 ♂♂ 1 ♀, NSMT); Aka, 4.v.2021, leg. R. Ito (1 ♂ 3 ♀♀, TUA). Fukaji Island : 3.v.2021, leg. R. Ito (6 ♂♂ 6 ♀♀, TUA). Geruma Island : 10.viii.1977, leg. S. Azuma (1 ♀, NSMT); 2.viii.2019, leg. H. Shigetoh (1 ♀, TUA); 4.v.2021, leg. R. Ito (4 ♂♂ 2 ♀♀, TUA). Kume Island : Une, Tonnaha-enchi, 27.iii.2018, leg. H. Yoshitake (1 ♀, NIAES); Daruma-yama, 28.iv.2018, leg. R. Ito (3 ♂♂ 4 ♀♀, TUA); Shirase-Riv., 29.iv.2018, leg. R. Ito (1 ♀, TUA); Yamashiro, 22-24.vii.2020, leg. H. Yoshitake (1 ♀, NIAES). Tokashiki Island : near Shuraku, 27.iv.2019, leg. H. Shigetoh (1 ♂, TUA); Tokashiki, 7.xi.2020, leg. J. Souma (2 ♂♂ 9 ♀♀, TUA); Aharen, 7.xi.2020, leg. J. Souma (2 ♂♂ 2 ♀♀, ELKU; 1 ♂ 3 ♀♀, TUA); Mt. Kumichizi , 8.xi.2020, leg. J. Souma (2 ♂♂ 4 ♀♀ 2 nymphs, TUA); Ôtani-path, 1.v.2018, leg. R. Ito (1 ♂ 2 ♀♀, TUA); Tokashiki, Ôtani road, 30.iv.2021, leg. R. Ito (1 ♀, TUA); as above but 1.v.2021 (4 ♂♂ 4 ♀♀, TUA). Tsuken Island : 16.iii.2019, leg. H. Shigetoh (1 ♀, TUA). Yabuchi Island : 5.iii.2020, leg. J. Souma (1 ♂ 1 ♀, TUA). Yagaji Island : Gabu, 9.iii.2020, leg. J. Souma (2 ♂♂ 2 ♀♀, TUA); Sumuide, 17.iv.2020, leg. H. Shigetoh (1 ♂, TUA). Zamami Island : near Mt. Odake , 20.iii.2020, leg. H. Shigetoh (1 ♂ 3 ♀♀, TUA); Asa Evacuation Route, 21.iii.2020, leg. H. Shigetoh (1 ♀, TUA); Ama, near Mt. Bansho , 21.iii.2020, leg. H. Shigetoh (1 ♂ 1 ♀, TUA); Inazaki-Kaminohama, 21.iii.2020, leg. H. Shigetoh (1 ♀, TUA); Ama, 3.vi.2020, leg. H. Shigetoh (1 ♀, TUA); Asa, 2.v.2018, leg. R. Ito (2 ♂♂ 2 ♀♀, TUA). Daito Islands : Kitadaito Island : Nakano, Daitôgû Shrine, 24.xi.2021, leg. T. Saeki (2 ♀♀, TUA). Minamidaito Island : Ikenosawa, 10.iii.2013, leg. H. Yoshitake (1 ♂ 1 ♀, NIAES); Zaisho, 6.vii.2014, leg. H. Ogai (5 ♂♂ 3 ♀♀, TUA); Daito Shrine, 9.ii.2018, leg. R. Ito (3 ♂♂ 2 ♀♀, TUA). Six specimens from Aka and Geruma islands collected in 1977 were considered to be recorded as " Stephanitis aperta " by a previous study ( Azuma and Kinjo 1987) GoogleMaps .

Diagnosis.

Stephanitis (Norba) exigua is recognised amongst other species of Stephanitis by a combination of the following characters: head, pronotal disc, marking on hemelytra and ventral surface in various shades of brown (Figs 7C View Figure 7 , 9C View Figure 9 , 11C View Figure 11 , 13C View Figure 13 , 15C View Figure 15 , 17C View Figure 17 , 19C View Figure 19 , 21C View Figure 21 , 23C View Figure 23 ); calli light brown; body in male 2.2 times (in female 2.1 times) as long as maximum width across hemelytra (Figs 2C View Figure 2 , 4C View Figure 4 ); rostrum not reaching metasternum; pronotum unicarinate (Fig. 25C View Figure 25 ); hood pale, shorter than median carina of pronotum, as wide as vertex at widest part, not covering eye, as high as median carina of pronotum at highest part, with posterior margin not extending to middle of pronotal disc; median carina of pronotum with 2 rows of areolae at highest part; pronotal disc lustrous; paranotum less erect, narrowed posteriorly, with 2 rows of areolae at widest part, with anterolateral angle slightly protruding anteriad, with outer margin gently curved inwards at posterolateral angle, maximum height shorter than height of eye (Fig. 27C View Figure 27 ); apices of hemelytra close to each other in rest; costal area with 3 rows of areolae at widest part; subcostal area with 2 rows of areolae at widest part; discoidal area with 3 rows of areolae at widest part; sutural area with 3-4 rows of areolae at widest part; hypocostal lamina with a single row of areolae throughout its length; R+M (radiomedial) vein carinate; pygophore elevated at centre of venter, with posterior margin slightly emarginate in middle part (Fig. 29C View Figure 29 ); and paramere stout, weakly curved inwards at apex, with outer margin not sinuate in middle part, inner margin nearly straight in basal part (Fig. 31C View Figure 31 ).

Remarks.

Amongst the Japanese species of Stephanitis , S. (Norba) exigua is similar to S. (N.) hiurai in general habitus, but the former is easily distinguished from the latter by the following characters: hood as wide as vertex at widest part (wider than vertex in S. (N.) hiurai ), not covering eye (incompletely covering in S. (N.) hiurai ) (Figs 7C, E, F View Figure 7 , 9C, E, F View Figure 9 , 25C, E View Figure 25 ); paranotum with 2 rows of areolae at widest part (3 rows in S. (N.) hiurai ), with anterolateral angle slightly protruding anteriad (protruding in S. (N.) hiurai ); costal area of hemelytron with 3 rows of areolae at widest part (4 rows in S. (N.) hiurai ) (Figs 15C, E, F View Figure 15 , 17C, E, F View Figure 17 ); subcostal area in female with 2 rows of areolae at widest part (3 rows in S. (N.) hiurai ); and R+M (radiomedial) vein in female carinate (not carinate in S. (N.) hiurai ).

Distribution.

Japan (Ryukyu Islands (central part): Okinawa Island, Aka Island, Fukaji Island, Geruma Island, Kume Island, Tokashiki Island, Tsuken Island, Yabuchi Island, Yagaji Island, Zamami Island; Daito Islands: Kitadaito Island, Minamidaito Island) (Fig. 45 View Figure 45 ); China ( Horváth 1912; Drake 1937; Takeya 1963; Miyamoto 1964a, 1964b; Azuma and Kinjo 1987; Yamada and Tomokuni 2012; Yamada and Ishikawa 2016; Nakatani 2021; present study). The previous record from Honshu ( Horváth 1912) is a misidentification of Stephanitis (Stephanitis) pyrioides . Hundreds of specimens from Honshu possessing the unicarinate pronotum were examined, but all of them belong to S. (Norba) aperta , S. (N.) mendica or S. (S.) tabidula . Therefore, S. (N.) exigua is probably not distributed in Honshu. The previous records from the southern part of the Ryukyu Islands and northern Taiwan ( Takeya 1963; Miyamoto 1964a, 1964b, 1964c; Azuma and Kinjo 1987; Hayashi 2002) correspond to S. (Norba) ishikawai sp. nov., described below. Hundreds of specimens from the southern part of the Ryukyu Islands possessing the unicarinate pronotum were examined, but all of them belong to S. (N.) ishikawai sp. nov. Therefore, S. (N.) exigua is probably not distributed in the southern part of the Ryukyu Islands. In Japan, S. (N.) exigua inhabits the laurilignosa in a subtropical climate of the central part of the Ryukyu Islands, which is in the Oriental Region.

Host plants.

Cinnamomum camphora , “Kusunoki” ( Lauraceae ) ( Takeya 1963; present study); C. yabunikkei H.Ohba, “Yabunikkei” (present study); Machilus thunbergii , “Tabunoki” ( Lauraceae ) (Fig. 43E View Figure 43 ) ( Takeya 1963; Yamada and Tomokuni 2012; present study). Stephanitis (Norba) exigua feeds only on lauraceous trees and is oligophagous. This lace bug sometimes occurs on plantings of C. camphora and M. thunbergii in its distribution range (present study), suggesting that it can become a pest of both lauraceous trees.

Biology.

Stephanitis (Norba) exigua feeds on the abaxial surface of leaves of the three host plants in Japan (present study). In Japan, adults were collected in almost all seasons ( Miyamoto 1964a, 1964b; present study); nymphs were collected in January, March and November (present study).

Kingdom

Animalia

Phylum

Arthropoda

Class

Insecta

Order

Hemiptera

Family

Tingidae

Genus

Stephanitis

Loc

Stephanitis (Norba) exigua Horvath , 1912

Souma, Jun 2022
2022
Loc

Stephanitis (Norba) exigua

Horvath 1912
1912
Loc

Stephanitis (Norba) aperta

Horvath 1912
1912