Research Article |
Corresponding author: Yong-Jin Sui ( syjkk2016@163.com ) Academic editor: Mike Wilson
© 2019 Yong-Jin Sui, Xiang-Sheng Chen.
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:
Sui Y-J, Chen X-S (2019) Review of the genus Vekunta Distant from China, with descriptions of two new species (Hemiptera, Fulgoromorpha, Derbidae). ZooKeys 825: 55-69. https://doi.org/10.3897/zookeys.825.31542
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The derbid genus Vekunta Distant, 1906 is reviewed. Two new species, V. bambusana sp. n. and V. pentaprocessusa sp. n., are described and illustrated from the southwest of China to give the genus twenty-nine species in China. A checklist and a key to species of the genus from China are also provided.
Cenchreini , distribution, Fulgoroidea , planthoppers, taxonomy
The planthopper family Derbidae (Hemiptera, Fulgoromorpha) was established by Spinola in 1839, containing three subfamilies in twenty tribes (
The planthopper genus Vekunta was established by
Herein, two new species, Vekunta bambusana sp. n. and V. pentaprocessusa sp. n., are described and illustrated from Guizhou and Yunnan provinces, China. A checklist and a key to species of the genus from China are also provided.
The morphological terminology follows
The type specimens are deposited in the Institute of Entomology, Guizhou University, Guiyang, Guizhou Province, China (GUGC).
Temesa Melichar, 1903: 40; preoccupied by Temesa (Mollusca) Adams, 1855.
Vekunta
Distant, 1906a: 8; 1906b: 287;
Temesa tenella Melichar, 1903 by original designation.
Combination of the following characters: head (Figs
V. albipennis Matsumura, 1914; China (Taiwan)
V. asymmetrica Liang & Wu, 2001; China (Xizang)
V. atripennis Matsumura, 1940; China (Taiwan)
V. bambusana sp. n.; China (Guizhou)
V. botelensis Matsumura, 1940; China (Taiwan)
V. commendata Yang & Wu, 1993; China (Taiwan)
V. diluta Yang & Wu, 1993; China (Taiwan)
V. extima Yang & Wu, 1993; China (Taiwan)
V. fera Yang & Wu, 1993; China (Taiwan)
V. gracilenta Yang & Wu, 1993; China (Taiwan)
V. intermedia Yang & Wu, 1993; China (Taiwan)
V. kotoshonis Matsumura, 1940; China (Taiwan)
V. lyricen Fennah, 1956; China (Taiwan)
V. maculata Matsumura, 1914; China (Taiwan)
V. makii Muir, 1914; China (Taiwan)
V. malloti Matsumura, 1914; China (Taiwan), Japan (Honshu, Kyushu, Shikoku)
V. memoranda Yang & Wu, 1993; China (Taiwan)
V. nigra Yang & Wu, 1993; China (Taiwan)
V. nigrolineata Muir, 1914; China (Taiwan)
V. nivea Fennah, 1956; China (Zhejiang)
V. nutabunda Yang & Wu, 1993; China (Taiwan)
V. obaerata Yang & Wu, 1993; China (Taiwan)
V. obliqua Yang & Wu, 1993; China (Taiwan)
V. parca Yang & Wu, 1993; China (Taiwan)
V. pentaprocessusa sp. n.; China (Yunnan)
V. shirakii Matsumura, 1914; China (Taiwan)
V. stigmata Matsumura, 1914; China (Taiwan)
V. triprotrusa Wu & Liang, 2001; China (Yunnan)
V. umbripennis Muir, 1914; China (Taiwan)
1 | Thorax with propleura with a large dark spot | V. albipennis |
– | Thorax with propleura not as above | 2 |
2 | Forewing along costal and anal margins with brown to dark brown stripe | 3 |
– | Forewing along costal and anal margins without brown to dark brown stripe | 6 |
3 | Female sternite VII with protrusion asymmetrical ( |
V. diluta |
– | Female sternite VII with protrusion symmetrical (Figs |
4 |
4 | Female sternite VII with protrusion length longer than width at base ( |
V. nigrolineata |
– | Female sternite VII with protrusion length shorter than width at base (Figs |
5 |
5 | Male with gonostyli bilaterally symmetrical (Fig. |
V. bambusana sp. n. |
– | Male with gonostyli asymmetrical, right gonostylus larger than left one (Fig. |
V. pentaprocessusa sp. n. |
6 | Forewing yellowish white | 7 |
– | Forewing pale brown, dark or with dark markings | 16 |
7 | Pygofer of male with dorsocaudal processes asymmetrical | 8 |
– | Pygofer of male with dorsocaudal processes symmetrical | 9 |
8 | Aedeagus of male not reaching to middle of periandrium ( |
V. nutabunda |
– | Aedeagus of male reaching to middle of periandrium ( |
V. commendata |
9 | Aedeagus of male with process(es) at base | 10 |
– | Aedeagus of male without process at base ( |
V. extima |
10 | Periandrium with 4–5 processes in male | 11 |
– | Periandrium with 2 processes in male | 13 |
11 | Periandrium with 5 processes in male ( |
V. maculata |
– | Periandrium with 4 processes in male | 12 |
12 | Periandrium of male with one pair of slender processes at base ( |
V. makii |
– | Periandrium of male with one spinous process at base ( |
V. nivea |
13 | Male with apical part of anal tube strongly curved in lateral profile | 14 |
– | Male with apical part of anal tube slightly curved in lateral profile | 15 |
14 | Periandrium of male with 2 short processes near middle, one directed caudally, another one directed dorsally ( |
V. gracilenta |
– | Periandrium of male with 2 long processes near middle, all directed caudally ( |
V. obliqua |
15 | Male with apical margin of anal tube broadly rounded; periandrium with short process at left base reaching less than middle ( |
V. intermedia |
– | Male with apical margin of anal tube truncate obliquely; periandrium with long process at left base reaching over than middle ( |
V. obaerata |
16 | Aedeagus of male, in right lateral view, with a small process near base and another lobe-like process in the middle ( |
V. parca |
– | Aedeagus of male not as above | 17 |
17 | Forewing with scattered dark markings | 18 |
– | Forewing uniformly dark except stigma | 22 |
18 | Mesothorax pale yellow | 19 |
– | Mesothorax fuscous or brown | 20 |
19 | Pygofer of male with symmetrical dorsocaudal processes; periandrium with one pair of stout processes at base ( |
V. lyricen |
– | Pygofer of male with asymmetrical dorsocaudal processes; periandrium without process at base ( |
V. kotoshonis |
20 | Frons between the lateral carinae reddish yellow | V. botelensis |
– | Frons between the lateral carinae brownish | 21 |
21 | Forewing veins very dark, paler toward apex | V. atripennis |
– | Forewing veins sordid yellow | V. shirakii |
22 | Hindwing black | 23 |
– | Hindwing not black | 26 |
23 | Antennae yellow | V. triprotrusa |
– | Antennae brown | 24 |
24 | Male with dorsocaudal processes of pygofer triangularly produced ( |
V. malloti |
– | Male with dorsocaudal processes of pygofer not triangularly produced | 25 |
25 | Aedeagus of male with 2 hooked processes at basoventral portion ( |
V. stigmata |
– | Aedeagus of male without hooked process at basoventral portion ( |
V. memoranda |
26 | Hindwing white | 27 |
– | Hindwing gray | 28 |
27 | Periandrium of male with a process at base ( |
V. fera |
– | Periandrium of male without process at base ( |
V. asymmetrica |
28 | Pygofer of male with dorsocaudal processes asymmetrical; periandrium without process at base ( |
V. umbripennis |
– | Pygofer of male with dorsocaudal processes symmetrical; periandrium with one pair of hooked processes at base ventrally and two long processes laterally, one process at base and another in the middle ( |
V. nigra |
Holotype ♂, CHINA: Guizhou, Wangmo, Dayi (25°22'N, 106°06'E), 21 August 2012, Z-M Chang. Paratypes, Guizhou: 1♂, Wangmo, Dayi, 23 August 2012, Z-M Chang; 2♂♂, Wangmo, Dayi, 13 August 2014, Z-M Chang; 3♂♂4♀♀, Wangmo, Dayi, 13–14 August 2014, Y Liu; 2♂♂, Suiyang, Wangcao (28°07'N, 107°16'E), 29 July 2014, H-Y Sun; 1♂, Suiyang, Wangcao, 29 July 2014, Y-J Wang.
Body length (including forewing): male 5.99–6.37 mm (n = 10), female 6.98–7.03 mm (n = 4); forewing length: male 5.02–5.45 mm (n = 10), female 5.96–6.02 mm (n = 4).
Coloration. General color yellow. Head (Figs
Head and thorax. Head (Figs
Vekunta bambusana sp. n., male. 5 Head and thorax, dorsal view 6 face 7 head and thorax, left lateral view 8 forewing 9 hindwing 10 genitalia, left lateral view 11 anal tube, dorsal view 12 dorsocaudal processes of pygofer, dorsal view 13 phallus, left lateral view 14 phallus, right lateral view. Scale bars: 0.5 mm (5–7); 0.2 mm (8–14).
Male genitalia. Anal tube (Fig.
Female genitalia. Anal tube (Figs
This species is similar to V. pentaprocessusa sp. n., but distinguished from the latter by: gonostyli (Fig.
The species name is derived from the host plant scientific name, Bambusoideae.
Bamboo.
China (Guizhou).
Holotype: ♂, CHINA, Yunnan: Mt Gaoligong National Natural Reserve (25°17'N, 98°48'E), light trap, 15 August 2013, Y- J Wang. Paratypes, Yunnan: 5♂♂1♀, same date as holotype; 3♂♂, Mt Gaoligong National Natural Reserve, light trap, 13 June 2011, J-K Long; 6♂♂2♀♀, Mt Gaoligong National Natural Reserve, light trap, 13–16 August 2013, W-C Yang, H-Y Sun, Y-J Wang; 1♂, Mt Gaoligong National Natural Reserve, light trap, 12 August 2018, L-J Yang.
Body length (including forewing): male 6.17–6.48 mm (n = 16), female 6.96–6.99 mm (n = 3); forewing length: male 5.36–5.40 mm (n = 16), female 6.04–6.11 mm (n = 3).
Coloration. General color yellow. Head (Figs
Head and thorax. Head (Figs
Male genitalia. Anal tube (Fig.
Vekunta pentaprocessusa sp. n., male. 20 Head and thorax, dorsal view 21 face 22 head and thorax, left lateral view 23 forewing 24 hindwing 25 male genitalia, left lateral view 26 anal tube of male, dorsal view 27 dorsocaudal processes of pygofer, dorsal view 28 phallus, left lateral view 29 phallus, right lateral view. Scale bars: 0.5 mm (20–22); 0.2 mm (23–29).
Female genitalia. Anal tube (Figs
This species is similar to V. fuscolineata
The new species name is derived from the Latin words penta- (five) and processus (process), referring to the apex of aedeagus with five processes in male.
Unknown.
China (Yunnan).
The genus Vekunta is a diverse genus in the subtropical and tropical regions of Australasian, Oriental, and Palaearctic regions (
Due to the original literature not recording host plants of this genus, many host plants are unknown. In our study, we find that V. bambusana sp. n. lives on bamboo in Guizhou, and some species of Vekunta we collected on weeds in some humid environments, for example, V. triprotrusa Wu & Liang, 2001. The new species V. pentaprocessusa sp. n. was collected by light trap. Thus, we speculate that this group prefers warm and moist environments and some species of the genus Vekunta have phototaxis. The natural environment of China is diverse, such as Yunnan Province (southern China), one of China’s richest regions in terms of biodiversity; however, only one species of genus Vekunta has been recorded in this region, so we believe there should be more species of this genus waiting to be discovered in this region and other parts of China.
The authors are grateful to the specimen collectors for their hard work in the field collections. This work was supported by the National Natural Science Foundation of China (No. 31472033), the Program of Excellent Innovation Talents, Guizhou Province (No. 20154021), the Program of Science and Technology Innovation Talents Team, Guizhou Province (No. 20144001), the International Cooperation Base for Insect Evolutionary Biology and Pest Control (No. 20165802), and the Program of Science and Technology Program in Guizhou Province (LH [2017] 7267).