Changwhania ceylonensis ( Baker , 1925 )
publication ID |
https://doi.org/ 10.5281/zenodo.187456 |
DOI |
https://doi.org/10.5281/zenodo.6224494 |
persistent identifier |
https://treatment.plazi.org/id/03A9F453-6C0F-2F2B-BB9F-B38FA051FE3E |
treatment provided by |
Plazi |
scientific name |
Changwhania ceylonensis ( Baker , 1925 ) |
status |
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Changwhania ceylonensis ( Baker, 1925) View in CoL
( Figs 3–6 View FIGURE 3 View FIGURE 4 View FIGURE 5 View FIGURE 6 , 9 View FIGURE 9 B–D, 9G, 9H)
Deltocephalus bimaculatus Melichar, 1903: 204 View in CoL , Sri Lanka; Kuoh, 1966: 128, China.
Deltocephaus ceylonensis Baker, 1925: 537 . Replacement name for Deltocephalus bimaculatus Melichar. View in CoL Cicadula bipunctatus, Singh-Pruthi, 1930: 59 , plate V, fig. 3. India. Synonymised by Webb & Heller, 1990: 8. Changwhania changwhani Kwon, 1980: 99 View in CoL , figs 1.8. Korea. Synonymised by Webb & Heller, 1990: 8. Changwhania ceylonensis Baker, Webb & Heller, 1990: 452 View in CoL .
Length (including tegmen), male: 2.6–2.7mm; female: 2.9–3.2mm.
General coloration pale yellowish orange to sordid yellow. Vertex pale yellowish orange, with two transversely oblong black markings near coronal margin, rarely markings joined medially or more rounded (see Remarks). Frontoclypeus with two black oval markings on each side just beneath antennal sockets. Pronotum and scutellum pale yellow to light brownish yellow without any striking transverse brown bands. Rostrum tip blackish. Tegmina pale yellow, subhyaline, Legs and venter pale yellowish orange to light brownish yellow. Female pregenital sternite with posterior medial lobe usually with black margin.
Male genitalia. Style apical process foot-like with a variable heel, the latter sometimes with a small to large triangular extension. Aedeagal shaft with rounded apex; with one short and one long apical process, latter variable in length (see Remarks), with or without a tooth near midlength.
Female seventh sternum produced lobe-like medially on posterior margin.
Material examined. JAPAN, 23, 2ƤƤ, Ryukyus, Yonguni Is., Higawa. M. Hayashi, 9.x.93 ( BMNH). KOREA: 13, Gyeongnam Prov., Mt Gajisan, 1.x.1984, Y.J. Kwon ( BMNH). INDIA: 1Ƥ, Nilgiri Hills, T.V. Campbell (syntype of Deltocephalus capitatus Distant ); 1Ƥ, Arun Valley, below Tumlingar, River Sabhaya, west shore, c.1800’, 22.xii.1961, dead leaves lying in sun on sandy shore; 13, Arun Valley, below Tumlingar, c. 1800’, 14.23. xii.1961, evergreen shrubs bordering dry stream beds ( BMNH). NEPAL: 13, Bhandar, 2,200m., 5.viii.1964; 3 3, 1Ƥ, Jiri, 2000m, 17.vi and 9.viii.64 ( BMNH). CHINA: Shaanxi Prov.: 1Ƥ, Xixiang, 1980. vii.29; 1Ƥ, Ankang, 1980. vii.29; 2ƤƤ, Yangling, 1986.vii; 13, Shangdong Prov., Laiyang, 500–800m, 2001. vii.22, coll.; 13, 4ƤƤ, Hubei Prov., County Fangxian, Town Jundian, 2001. vii.30, coll. He Zhiqiang; 1Ƥ, Sichuan Prov., Huanglong, 1980. vii.02; Hunan Prov., Chenzhou: 13, 4ƤƤ, 1985. vii.23; 13, 1985. viii.03, Jiangxi Prov.: Pingxiangfanglou: 13, 2002. viii.05; 3ƤƤ, 2002. viii.05; Shangrao, Mt. Qianshan: 2ƤƤ, 2002. viii.13; 13, 8ƤƤ, 80m, 2006. viii.31; 1Ƥ, Fujian Prov., County Shanghang, 2003. viii.16,; Guangxi Autonomous Region: 1Ƥ, Park Shiwandashan, 2001. xi.30, coll.; 5ƤƤ, Xinzhai, 900m, 2006. viii.18,; Guangdong Prov.: Dianbai: 1Ƥ, 1983. iv.08; 13, 2ƤƤ, 1983. iv.10; 13, 4ƤƤ, 1983. iv.11; 2ƤƤ, 1983. iv.12; 13, 4ƤƤ, 1983. iv.13; 2ƤƤ, Shenzhen, 1983. iv.18; 1Ƥ, Mt. Dinghu, 1983. vii.17; Sichuan Prov., 33, 1Ƥ, Batang, Zhubalong, 2450m, 2001. vii.12, coll. Sun Qiang; 13, 1Ƥ, Mianning, 1650m, 1999.viii, coll. I. Dworakowska; Hainan Prov.: 1Ƥ, Xinglong, 1983. iv.27; 1Ƥ, Changjiang, 1983. vi.22; Bawangling: 13, 1983. vi.24,; 2ƤƤ, 1983. vi.26; Liangyuan: 23, 1983. vi.29; 1Ƥ, 1983. vi.31; 13, 4ƤƤ, 1983. vi.01; 1Ƥ, 1983. vi.02,; 13, 1983. vi.07; Qiongzhong: 3ƤƤ, 1983. vi.04; 1Ƥ, 1983. vi.05; 1Ƥ, Tongshen, 1983. vi.07. Various collectors (Zhang Yalin, Yang Meixia, Ma Ning, Chai Yonghui, Qin Daozheng, Liu Zhenjiang, Sun Qinxia, Yuan Zhonglin, Duan Yani, Wang Zongqing), at light or without further information ( NWAFU). THAILAND: 33, 5ƤƤ, Chiengmai, uppland rice, v.1982; 23, 1Ƥ, Lopburi, vi.1974; 13 ( BMNH). PHILIPPINES: 13, Malangol, Kalinga, 8.iv.1972, A.D. Pawar; 13, Luzon, Albay Prov., Guinobatan, 2.3. viii.1978 ( BMNH); 33, 1Ƥ, Mountain Prov., Abatan, Buguias, 1800–2000m., iv, v.1964, H.M. Torrevillas; 2ƤƤ, Luzon, La Trinidad, 4–5.iv.1968, D.E. Hardy; 1Ƥ, Tifalmin, 1400m., 21.viii.1963, R. Straatman, light trap ( BPBM). PAPUA NEW GUINEA: 13, W. Sepik, 19.xi.1985, J.W. Ismay, on taro ( BMNH). NEW CALEDONIA: 33, hills behind Noumea, 17.vii.1940, F.X. Williams ( BPBM).
Distribution. Korea, Japan, Nepal, India, Sri Lanka, China, Thailand, Philippines, Papua New Guinea, New Caledonia.
Remarks. This species can be distinguished externally by the oblong black spots on the vertex and narrow black patch below each antennal base ( Figs 9 View FIGURE 9 B–D, 9G, 9H, 4A, 4B), and in the male genitalia by the typically foot-like apical process of the style ( Figs 3 View FIGURE 3 C, 4E–H) or with a triangular distal extension ( Figs 5 View FIGURE 5 D, 5E, 6E) and apical position of one or both of the aedeagal process ( Figs 3 View FIGURE 3 D, 4I-N, 5F, 5G, 6F, 6G). This identity, which resulted in the above synonymy by Webb & Heller (1990), is based on associating males to the female types of ceylonensis with similar shaped head spots. However, based on the material examined in this study, in some specimens the spots in ceylonensis approach those of terauchii , i.e. are more rounded. Adding to this difficulty of separating the two species on external appearance is the fact that two species have similar distributions and females of all species of the genus have an identical medial lobed pregenital sternite. Also, in specimens from New Caledonia the vertex spots are distinctly rounded and relatively large, and in one specimen from India (Arun Valley) the head spots coalesce to form a transverse band as described by Distant (1918) for part of the syntype series of C. distanti ( Baker) i.e. that from Kodaicanal, India (specimen(s) not found). In addition, the material from Thailand, Nepal, Philippines (Abatan) and China (Sichuan Province) show more extreme variation of the male genitalia than in some other specimens, i.e. the apex of the style is extended either into a triangular lobe ( China, Figs 5 View FIGURE 5 E, 6E) or is foot-like with a well developed heel (remainder, Fig. 4 View FIGURE 4 E), one aedeagal process is much longer ( Figs 4 View FIGURE 4 N, 5F, 5G, 6F, 6G), the pygofer processes is truncate ( Philippines) and the anal tube process is acute ( Thailand) or bifurcate ( Nepal). In contrast, some specimens on the south eastern fringes of the distribution i.e. from New Guinea and New Caledonia (see Material examined) have more typical male genitalia as in fig. 3.
No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.
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Genus |
Changwhania ceylonensis ( Baker , 1925 )
Zhang, Yalin & Duan, Yani 2009 |
Deltocephaus ceylonensis
Webb 1990: 8 |
Webb 1990: 8 |
Webb 1990: 452 |
Kwon 1980: 99 |
Singh-Pruthi 1930: 59 |
Baker 1925: 537 |
Deltocephalus bimaculatus
Kuoh 1966: 128 |
Melichar 1903: 204 |