Research Article |
Corresponding author: Yalin Zhang ( yalinzh@nwsuaf.edu.cn ) Corresponding author: Min Huang ( huangmin@nwsuaf.edu.cn ) Academic editor: Mick Webb
© 2022 Xian Zhou, Yalin Zhang, Min Huang.
This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Citation:
Zhou X, Zhang Y, Huang M (2022) New leafhopper species and new records of Typhlocybini (Hemiptera, Cicadellidae, Typhlocybinae) from China. ZooKeys 1082: 135-151. https://doi.org/10.3897/zookeys.1082.73611
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Five genera from China of the leafhopper tribe Typhlocybini are treated. Linnavuoriana Dlabola, 1958 and Shamala Dworakowska, 1980 and seven known species, Edwardsiana corylicola Vilbaste, 1968, E. praedestina Dlabola, 1967, E. singularis Anufriev, 1975, Hiratettix distanti Dworakowska, 1982, H. malaisei Dworakowska, 1982, L. antiqua Dworakowska, 1982, and L. malicola Zachvatkin, 1949 are newly recorded from China. Two new species, Shamala annulata and Paracyba biprocessa spp. nov., are described and illustrated. Keys to Chinese species of each genus are also provided.
Auchenorrhyncha, distribution, morphology, taxonomy, Typhlocybini
Typhlocybini (Hemiptera, Cicadellidae, Typhlocybinae) is a moderately large leafhopper tribe with over 924 species in 93 genera worldwide, of which 253 species in 44 genera have been recorded from China (including Zyginellini) (
Figures of the specimens were made using a Leica M205 light microscope with a Leica DFC425 camera. Images were produced using the Leica Application Suite V3.7 and edited using Adobe Photoshop CS6.0 (Adobe Systems). Abdomens were removed from examined specimens and macerated in cold 10% NaOH solution overnight, subsequently rinsed for 30 s with pure water, and stored in glycerin. An Olympus SZX10 microscope was used for dissecting specimens and an Olympus PM-10AD was used for drawing the dissected male genitalia.
Morphological terminology in this work follows
Type specimens of the new species are deposited in the collections of the Entomological Museum, Northwest A&F University, Yangling, China (NWAFU).
Edwardsiana Zachvatkin, 1929: 439.
Cicada rosae Linnaeus, 1758, by original designation.
The genus Edwardsiana includes 80 known species worldwide (
Body cream with variable patches (Figs
Typhlocybini of China 1–5 dorsal view 6–10 head and thorax, dorsal view 11–15 lateral view 16–20 face 1, 6, 11, 16 Edwardsiana corylicola 2, 7, 12, 17 E. praedestina 3, 8, 13, 18 E. singularis 4, 9, 14, 19 Hiratettix distanti 5, 10, 15, 20 H. malaisei. Scale bars: 1.0 mm (1–5, 11–15); 0.5 mm (6–10, 16–20).
Male sternal abdominal apodemes well developed, often extending to middle of 6th sternite.
Male genitalia. Pygofer side often with rounded extension at basal angle; ventral part always with depressed areas, dense stout setae on ventral-basal part and row of short rigid setae caudally. Subgenital plate elongate with subapical part twisted outwards; long macroseta basally and row of short rigid setae from middle to subapex. Paramere with distal part long and curved. Connective with central ridge developed. Aedeagus with preatrium and dorsal apodeme developed; aedeagal shaft with paired apical processes; gonopore apical.
Palaearctic and Nearctic regions.
1 | Aedeagal shaft with two pairs of unbranched apical processes | E. rosae (Linnaeus) |
– | Aedeagal shaft with apical processes branched | 2 |
2 | Aedeagal shaft with both dorsal and ventral processes branched (Figs |
E. singularis Anufriev |
– | Aedeagal shaft just with dorsal processes branched | 3 |
3 | Ventral processes of aedeagal shaft short and directed ventrad (Figs |
E. corylicola Vilbaste |
– | Ventral processes of aedeagal shaft long and directed dorsad | 4 |
4 | Aedeagal shaft with dorsal and ventral processes branched near base (Figs |
E. praedestina Dlabola |
– | Aedeagal shaft with dorsal and ventral processes branched at middle or near apex | E. ishidai (Matsumura) |
Edwardsiana corylicola
Vilbaste, 1968: 98,
2♂♂, 2♀♀, China, Heilongjiang Province, Mishan, 2.ix.2001, coll. Qiang Sun.
China (Heilongjiang), Russia, Korea, North Korea.
Typhlocyba ishidai Matsumura, 1932: 98, pl. II, fig. 3a, b.
Typhlocyba lanternae Wagner, 1937: 154.
Edwardsiana ussurica Vilbaste, 1968: 97.
Edwardsiana ishidai
(Matsumura):
China (Jilin), Japan, Mongolia, Russia.
Edwardsiana praedestina Dlabola, 1967: 217, figs 12–14.
1♂, 19♀♀, China, Shandong Province, Kunyu Mountain, 12.vii.2001, coll. Daozheng Qin and Zhenjiang Liu.
China (Shandong), Mongolia.
Cicada rosae Linnaeus, 1758: 439.
Edwardsiana subrosea Vilbaste, 1980: 41.
Edwardsiana rosae
(Linnaeus):
China (Gansu, Xinjiang), Cyprus, Turkey, Iran, Russia, Kazakhstan, Kirghizstan, Uzbekistan, Tajikistan.
Edwardsiana singularis
Anufriev, 1975: 531;
1♂, China, Heilongjiang Province, Mishan, 2.ix.2001, coll. Qiang Sun.
China (Heilongjiang), Russia, Kazakhstan.
Hiratettix
Matsumura, 1931: 59 (in key);
Hiratettix arisanellus Matsumura, 1932.
After
Body flat and overall black (Figs
Male genitalia. Genital capsule high and short. Pygofer with several short rigid setae terminally on inner surface and long macrosetae ventrobasally. Subgenital plate broad basally, slightly narrowed distally, with several long macrosetae near middle part, a row of short rigid setae laterally and progressively shorter subbasally to apex. Connective wide with central lobe underdeveloped. Paramere thick with central part longer than basal and distal parts together; caudal part with sensorial pits on inner margin. Aedeagal shaft with paired apical and lateral processes; gonopore apical.
Oriental Region.
1 | Aedeagal shaft with two long basal processes and two pairs of short apical processes | 2 |
– | Aedeagal shaft with two medium sized lateral processes and one pair of short apical processes | 3 |
2 | Aedeagal shaft with basal processes S-bent and two pairs of apical processes basally closed | H. arisanellus Matsumura |
– | Aedeagal shaft with basal processes arched and two pairs of apical processes detached from each other basally | H. matsumurai Dworakowska |
3 | Aedeagal shaft with median processes curved outwards, apical processes directed to each other distally (Figs |
H. distanti Dworakowska |
– | Aedeagal shaft with median processes straight, apical processes widely separated distally (Figs |
H. malaisei Dworakowska |
Hiratettix arisanellus
Matsumura, 1932: 102;
China (Taiwan).
Hiratettix distanti
1♂, China, Yunnan Province, Mengla, Nangong Mountain, 1850 m, 13.xii.1999, coll. Dworakowska.
China (Yunnan), India.
Hiratettix malaisei
1♂, China, Sichuan Province, Emei Mountain, 950 m, 30.x.1999, coll. Dworakowska. 1♂, 2♀♀, China, Guizhou Province, Huaxi, Huaxi Garden, 1100 m, 25.vii.2001, coll. Qiang Sun, at light. 1♂, 14♀♀, China, Yunnan Province, Shilin, 9.vii.2021, coll. Xian Zhou.
China (Sichuan, Guizhou, Yunnan), Myanmar.
Hiratettix matsumurai
China (Taiwan).
Linnavuoriana
Cicada decempunctata Fallen, 1806.
Up to now, there are eight known species in the genus Linnavuoriana. In Xinjiang and Yunnan provinces, we collected two known species that are the first records of the genus from China. A key to the Chinese species is given.
Body cream, light yellow (Figs
Typhlocybini of China 21–24 dorsal view 25–28 head and thorax, dorsal view 29–32 lateral view 33–36 face 21, 25, 29, 33 Linnavuoriana antiqua 22, 26, 30, 34 L. malicola 23, 27, 31, 35 Paracyba biprocessa sp. nov. 24, 28, 32, 36 Shamala annulata sp. nov. Scale bars: 1.0 mm (21–24, 29–32); 0.5 mm (25–28, 33–36).
Head bluntly produced, little narrower than width of pronotum, and 1/3 times middle length of pronotum (Figs
Abdominal apodemes well developed, often extending to 5th abdominal sternite.
Male genitalia. Hind margin of pygofer with inner ridge, several rigid microsetae near posterior-dorsal margin and numerous minute tubercles posteroventrally. Subgenital plate parallel-sided and lack macrosetae at base, narrowing from apical 1/3–1/2 of outer margin, rounded terminally, usually with row of rigid microsetae and some fine microsetae scattered on apex. Paramere rarely curved with subapical tooth; distally with row of microsetae on outer margin and row of sensorial pits on inner margin. Connective small with central ridge underdeveloped. Aedeagal shaft with a pair of triangular protrusions on dorsal surface laterally; gonopore apical.
Oriental and Palaearctic regions.
1 | Crown and pronotum with large dark patches; aedeagal shaft with apex hook-like (Figs |
L. antiqua Dworakowska |
– | Crown and pronotum with few light patches; aedeagal shaft with apex not hook-like (Figs |
L. malicola (Zachvatkin) |
Linnavuoriana antiqua
1♂, 1♀, China, Yunnan Province, Lijiang, Xinzhu Botanical Garden, 16.xi.1999, coll. Dworakowska. 1♂, Yunnan Province, Tengchong, 1650 m, 26.iv.1981, coll. Fasheng Li.
China (Yunnan), India.
Typhlocyba malicola Zachvatkin, 1949: 220.
Linnavuoriana taschkentica
Dlabola, 1961: 302, figs 152–156. Synonymized by
Linnavuoriana apunctata Mitjaev, 1963: 49, nec Dlabola.
Typhlocyba roseipennis
Kusnezov, 1932: 232, nec Oshanin (
Linnavuoriana populicola
Dubovsky, 1966: 132; Synonymized by
4♂♂, 3♀♀, China, Xinjiang Province, Xinjiang Agricultural Vocational and Technical College, 16.ix.1986, coll. Yalin Zhang. 13♂♂, 4♀♀, Xinjiang Agricultural University, 16.ix.1986, coll. Yalin Zhang.
China (Xinjiang), Kazakhstan, Kirghizstan, Uzbekistan, Tajikistan, Afghanistan.
Paracyba
Vilbaste, 1968: 96;
Zygina akashiensis Takahashi, 1928.
Until now, the genus Paracyba included three known species, including two species from China. Here we add a new species from China and give a key to all species of the genus.
Body slim. Head bluntly produced, middle length equal to or shorter than width between eyes, coronal suture long and distinct. Forewing laterally with apex rounded; RP and MP’ petiolate at base; 1st apical cell nearly equal in size to 4th apical cell; 2nd apical cell biggest. Hind wing with two cross veins.
Male sternal abdominal apodemes extending to distal margin of 4th sternite.
Male genitalia. Pygofer side tall and divided into two or three small lobes caudally, upper lobe and central lobe with short rigid setae terminally, lower lobe deeply contracted, usually with long macrosetae. Subgenital plate elongate, triangular with a row of short fine setae subbasally to apex, with indistinct peg-like setae at apex. Paramere with basal part slim and central part broad, thereafter gradually tapered to apex, with a row of microsetae on outer margin. Connective trapezoidal. Aedeagus with short preatrium; dorsal apodeme well developed bifurcate apically; aedeagal shaft usually short with long and asymmetrical processes apically; gonopore apical.
Oriental and Palaearctic regions.
1 | Aedeagal shaft with two distal processes (Figs |
P. biprocessa sp. nov. |
– | Aedeagal shaft with three distal processes | 2 |
2 | Aedeagus with lateral process arising from mid-length of shaft; two other processes slightly arched, longest process bent to right | P. akashiensis (Takahashi) |
– | Aedeagus with lateral process arising near apex; other two processes relatively straight, longest process bent to left | 3 |
3 | Two apical processes of aedeagus twice as long as subapical process | P. soosi Dworakowska |
– | Two apical processes of aedeagus nearly equal in length to subapical process | P. nopporensis Matsumura |
Zygina akashiensis
Takahashi, 1928: 442;
China (Taiwan), Japan, Russia.
Paracyba soosi Dworakowska, 1977: 41, figs 253–259.
China (Hunan), Vietnam.
Typhlocyba nopporensis
Matsumura, 1932: 100;
Japan, Russia.
Head with coronal suture extended to anterior margin (Fig.
Male sternal abdominal apodemes extending to middle of 5th sternite (Fig.
Pygofer side tall and bilobate caudally, upper lobe with short setae terminally, lower lobe with several fine moderately long setae (Fig.
Holotype : ♂, China, Shaanxi Province, Yangling, ix.1983, coll. Yalin Zhang. Paratypes: 10♂♂, 4♀♀, same data as holotype.
Male, 3.1–3.3 mm (including wing).
This new species is named for the two aedeagal processes, rather than three in other species.
This new species resembles Paracyba soosi Dworakowska, 1977 in coloration and male genitalia, but it differs from the latter in aedeagal shaft having two rather than three distal processes and processes of very different length.
Shamala Dworakowska, 1980: 169, figs 174–187.
Shamala mikra Dworakowska, 1980.
The genus Shamala was erected by
Male genitalia and sternal abdominal apodemes of Paracyba biprocessa sp. nov. 55 sternal abdominal apodemes 56 genitalia capsule, lateral view 57 paramere, connective and subgenital plate, dorsal view 58 subgenital plate 59 paramere 60 aedeagus, lateral view 61 aedeagus, posterior view 62 apical part of aedeagus, dorsal view.
Body slim and cream with occasional light brown patches. Head slightly wider than pronotum with length along midline slightly shorter than distance between eyes. Forewing parallel-sided, rounded terminally; RP and MP’ petiolate at base. Hind wing gradually narrowing from base to apex and rounded terminally with two cross veins.
Male sternal abdominal apodemes extending to 4th or 5th sternite.
Male genitalia. Genital capsule short; pygofer side with a weekly sclerotized area near middle of hind margin; several rigid setae at caudo-ventral angle and macrosetae on middle part. Subgenital plate gradually narrowing towards apex with a macroseta at base and row of short peg-like setae from middle to apex of outer margin; two rigid setae apically and few fine setae on inner margin subapically. Connective laminate, with stem well developed. Paramere with caudad part long, with several setae on outer margin. Aedeagal shaft with distal asymmetrical processes; with long membranous terminal part.
Oriental Region.
Body cream (Fig.
Abdominal apodemes extending to distal margin of 4th sternite.
Male genitalia. Pygofer side with several macrosetae ventrally and rigid short setae terminally (Figs
Holotype : ♂, China, Yunnan Province, Sanchahe, 7.vi.1991, coll. Rungang Tian. Paratypes: 3♂♂, same data as holotype.
Male, 2.94 mm (including wing).
The name of this species is derived from the Latin word “annulus”, referring to the two dorsal processes of the aedeagal shaft forming a ring-like shape.
This new species resembles Shamala ricasta Dworakowska, 1981 in the structure of the male genitalia, but it differs from the latter by the two longer apical processes of aedeagal shaft forming a ring-like shape.
We are very grateful to Dr I. Dworakowska for her contribution to the knowledge of Chinese Typhlocybinae. We give sincere thanks to students in the Entomological Museum of Northwest A&F University for their great help in obtaining specimens. We also thank Prof. John Richard Schrock (Emporia State University, USA) for proofreading of the manuscript and giving us valuable advice before submission. We extend our heartfelt gratitude to Mick Webb and Valérie Lemaître (The Natural History Museum, London, UK) and anonymous reviewers for their earnest reviews. This study is supported by the National Natural Science Foundation of China (32070478, 31372233, 31420103911) and The Ministry of Science and Technology of the People’s Republic of China (2006FY120100, 2015FY210300).