Biodiversity Data Journal :
Taxonomic Paper
|
Corresponding author: Yuehua Song (songyuehua@163.com)
Academic editor: Yasen Mutafchiev
Received: 14 Jun 2021 | Accepted: 19 Aug 2021 | Published: 25 Aug 2021
© 2021 Xiao Yang, Guimei Luo, Yuehua Song
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:
Yang X, Luo G, Song Y (2021) Two new species of Erythroneurini from China (Hemiptera, Cicadellidae, Typhlocybinae). Biodiversity Data Journal 9: e70141. https://doi.org/10.3897/BDJ.9.e70141
|
The leafhopper genus Empoascanara Distant, 1918 encompasses 81 species, most of which are distributed in Afrotropical, Oriental and Australian Realm. The leafhopper genus Kapsa Dworakowska, 1972 encompasses 23 species, mainly known from the Oriental and Australian Realms.
Two new species of the leafhopper tribe Erythroneurini from Guizhou Province, China, Empoascanara dichotomus sp. nov. and Kapsa sinuose sp. nov. are described and illustrated. Identification keys to the males of the genera Empoascanara and Kapsa in China are proposed.
Cicadomorpha, Auchenorrhyncha, leafhopper, taxonomy, Karst
The leafhopper genus Empoascanara Distant, 1918 was established with Empoascanara prima Distant, 1918 as its type species. So far, 81 species of the genus Empoascanara have been reported, most of which are distributed in Africa, the Orient and Australia. The leafhopper genus Kapsa Dworakowska, 1972 was established with Typhlocyba furcifrons Jacobi, 1941 as its type species (
The specimens were obtained by sweep net and morphological terminology used in this work follows
Body length male 2.1-2.3 mm; female 2.2-2.4 mm. Vertex brownish-yellow, with one irregular spot near anterior margin (Fig.
Male genitalia. Pygofer lobe with scattered microsetae at right edge. Dorsal pygofer appendage process without branch. Subgenital plate (Fig.
The specific name is derived from the Latin word “dichotomus” (bifurcated), referring to the bifurcated processes on the aedeagal shaft in the ventral view (Fig.
Empoascanara dichotomus is characterised with the morphology of the genus Empoascanara as follows:
Crown fore margin strongly produced and angulate medially or weakly produced, broadly rounded apically. Vertex usually with pair of dark pre-apical spots or with large median apical patch. Pronotum pale or almost entirely dark or with dark posterior margin. Forewing with venation of clavum obscure.
Male pygofer lobe rounded or angulate, without dorsal macrosetae, with sparse long fine setae. Pygofer dorsal appendage movably articulated, ventral appendage absent. Subgenital plates free, lateral margin with angulate sub-basal projection, with 2–4 basal macrosetae and distinct marginal sub-basal rigid setae forming continuous row or with marginal sub-basal rigid setae restricted to basolateral angle. Style pre-apical lobe prominent. Style apex smooth, slender or truncate and expanded, third point absent. Aedeagus dorsal apodeme not expanded in lateral view; shaft curved dorsad, smooth or denticulate distally; apex broadened, truncate or acuminate in ventral view; ventral processes placed basally, well separated from shaft. Connective median anterior lobe broad, arms short.
Empoascanara dichotomus is similar to Empoascanara thomasi Dworakowska, 1979; however, the new species has an aedeagus with a pair of processes on the apex instead of on the subapex and processes apex branched and the more chitinised aedeagus.
Crown has anterior region yellow, while posterior area is yellow-milky, wider than pronotum. Face yellow, relatively long, with anteclypeus yellow (Fig.
Male genitalia. Pygofer lobe with scattered microsetae at right edge (Fig.
The specific name is derived from the Latin word “ramosis”, which means that species have two processes on the aedeagal shaft in the ventral side view (Fig.
The new species, Kapsa ramosis, has the following morphological characters that places it within the subgenus Kapsa (see also
Male pygofer not extended to apex of subgenital plate. Pygofer lobe rounded. Pygofer ventro-apical membranous area well developed. Subgenital plate lateral margin with angulate sub-basal projection. Subgenital plates free. Style pre-apical lobe prominent. Style apex truncate and expanded or with 3 points. Aedeagus with pre-atrium shorter than shaft or with pre-atrium about as long as shaft. Aedeagus without dorsal process or with processes on dorsal apodeme. Connective median anterior lobe broad. Connective stem absent or very short, depressed.
Kapsa ramosis is similar to K. furcifrons (Jacobi, 1941), but differs from it by having aedeagus with processes and the three macrosetae instead of five macrosetae on lateral surface centrally.
Key to the males of Empoascanara in China (modified after Song and Li 2013) |
||
1 | Aedeagal shaft without processes | 2 |
– | Aedeagal shaft with processes | 5 |
2 | Aedeagus dorsal apodeme large, expanded | 3 |
– | Aedeagus dorsal apodeme small, indistinct (Fig. |
E. alami Dworakowska |
3 | Gonopore apical (Fig. |
E. sonani Dworakowska |
– | Gonopore subapical or median | 4 |
4 | Aedeagal shaft with apex broad; gonopore subapical (Fig. |
E. lata Dworakowska & Pawer |
– | Aedeagal shaft with apex narrow; gonopore median (Fig. |
E. kotoshonis Dworakowska |
5 | Aedeagus with basal atrial processes | 6 |
– | Aedeagus without basal atrial processes | 12 |
6 | Aedeagal shaft with apex bifurcate | 7 |
– | Aedeagal shaft with apex not bifurcate | 8 |
7 | Basal atrial processes of aedeagus bifurcate (Fig. |
E. penta Dworakowska |
– | Basal atrial processes of aedeagus not bifurcate (Fig. |
E. limbata Dworakowska |
8 | Aedeagal shaft short and pre-atrium long | 9 |
– | Aedeagal shaft long and pre-atrium short | 11 |
9 | Basal atrial processes of aedeagus with lateral margin serrate apically (Fig. |
E. circumscripta Chiang & Knigh |
– | Basal atrial processes of aedeagus with lateral margin smooth apically | 10 |
10 | Pygofer dorsal appendage expanded at base, then narrowed abruptly and bifurcate at apex (Fig. |
E. nigrobimaculata Dworakowska |
– | Pygofer dorsal appendage broad and short, nearly equal to width and bifurcate at apex (Fig. |
E. sipra Dworakowska |
11 | Gonopore apical on ventral surface (Fig. |
E. conchata Song & Li |
– | Gonopore sub-basal on ventral surface (Fig. |
E. mai Dworakowska |
12 | Aedeagal shaft with paired apical processes | 13 |
– | Aedeagal shaft with unpaired apical processes | 14 |
13 | Gonopore at apex (Fig. |
E. dwalata Dworakowska |
– | Gonopore at sub-apex | 17 |
14 | Pygofer dorsal appendage not branched apically (Fig. |
E. longiaedeaga Song & Li |
– | Pygofer dorsal appendage branched apically | 15 |
15 | Apical processes of aedeagal shaft lamella-like (Fig. |
E. fumigata Dworakowska |
– | Apical processes of aedeagal shaft band-like | 16 |
16 | Aedeagal shaft with 3 asymmetrical apical processes (Fig. |
E. hongkongica Dworakowska |
– | Aedeagal shaft with 2 asymmetrical apical processes (Fig. |
E. maculifrons Dworakowska |
17 | Aedeagus with a pair of not bifurcate processes arising from apex of shaft (Fig. |
E. mana Dworakowska |
– | Aedeagus with a pair of bifurcate processes arising from apex of shaft | E. dichotomus sp. nov. |
Мale genitalia of Empoascanara spp. A E. alami, Aedeagus, lateral view; B E. sonani, aedeagus, ventral view; C E. lata, aedeagus, ventral view; D E. kotoshonis, aedeagus, ventral view; E E. penta, аedeagus, ventral view; F E. limbata, aedeagus, ventral view; G E. circumscripta, aedeagus, ventral view; H E. nigrobimaculata, pygofer lobe, lateral view; I E. sipra, pygofer lobe, lateral view; J E. conchata, aedeagus, ventral view; K E. mai, aedeagus, ventral view; L E. dewalata, aedeagus, ventral view; M E. longiaedeaga, aedeagus, ventral view; N E. hongkongica, aedeagus, ventral view; O E. maculifrons, aedeagus, lateral view; P E. mana, aedeagus, ventral view; Q E. fumigata, aedeagus, lateral view.
Key to the males of Kapsa (Kapsa) in China (modified after Song and Li 2012) |
||
1 | Aedeagus with processes | 2 |
– | Aedeagus without processes | 5 |
2 | Aedeagus with both basal and apical processes (Fig. |
K. quadrispina Song & Li |
– | Aedeagus either with basal processes or apical processes | 3 |
3 | Pygofer with dorsal appendage bifurcate | 4 |
– | Pygofer with dorsal appendage not bifurcate (Fig. |
K. biprocessa Song & Li |
4 | Gonopore long (Fig. |
K. acuminata Song & Li |
– | Gonopore moderately long | K. ramosis sp. nov. |
5 | Aedeagus with dorsal apodeme short and small, not expanded in lateral view (Fig. |
K. fangxianga Song & Li |
– | Aedeagus with dorsal apodeme large, greatly expanded in lateral view | 6 |
6 | Aedeagal shaft moderately long (Fig. |
K. arca Song et al. |
– | Aedeagal shaft moderately short | 7 |
7 | Aedeagal shaft slender and sinuate (Fig. |
K. dolka Dworakowska |
– | Aedeagal shaft broad and straight (Fig. |
K. suaoensis Chiang & Knight |
Мale genitalia of Kapsa spp. A K. quadirispina, aedeagus and connective, ventral view; B K. biprocessa, aedeagus, ventral view; C K. acuminata, аedeagus, ventral view; D K. fangxianga, aedeagus and connective, ventral view; E K. arca, аedeagus, ventral view; F K. suaoensis, aedeagus, connective and style, ventral view; G K. dolka, aedeagus, ventral view.
This study was partly funded by the World Top Discipline Program of Guizhou Province: Karst Ecoenvironment Sciences (No.125 2019 Qianjiao Keyan Fa), the Guizhou Provincial Science and Technology Foundation ([2018]1411), the Guizhou Science and Technology Support Project ([2019]2855), the Science and Technology Project of Guiyang City ([2020]7-18), the Innovation Group Project of Education Department of Guizhou Province ([2021]013), the Training Program for High-level Innovative Talents of Guizhou Province ([2016]4020) and the Project for Regional Top Discipline Construction of Guizhou Province: Ecology in Guiyang University [Qian Jiao Keyan Fa [2017]85].