Coeliccia scutellum Laidlaw, 1932
publication ID |
https://doi.org/ 10.11646/zootaxa.4059.2.2 |
publication LSID |
lsid:zoobank.org:pub:5D7E8244-3A68-40A7-ABCF-8932C6492948 |
DOI |
https://doi.org/10.5281/zenodo.6100439 |
persistent identifier |
https://treatment.plazi.org/id/D04487FB-A679-FFBE-FF78-F973FCB9151E |
treatment provided by |
Plazi |
scientific name |
Coeliccia scutellum Laidlaw, 1932 |
status |
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Coeliccia scutellum Laidlaw, 1932 View in CoL
Coeliccia tomokunii Asahina, 1997 View in CoL has been considered a junior synonym of C. scutellum Laidlaw, 1932 ( Wilson & Reels 2001) View in CoL . Asahina (1997: 24) indicated this possibility in his original description of C. tomokunii View in CoL and suggested that “...a careful comparison of the type specimen is needed between the two species.” In order to test this possible synonymy we compared the lectotype of C. scutellum View in CoL with specimens that were collected near the type locality of C. tomokunii View in CoL , since the type specimens of C. tomokunii View in CoL are not accessible and may be lost.
Descriptions and illustrations of specimens are provided and compared with the original descriptions by Laidlaw (1932) and Asahina (1997). Laidlaw (1932) gave only a short description and a rough sketch of the thoracic markings of C. scutellum View in CoL , whereas Asahina's (1997) description includes illustrations of the head, thorax and anal appendages of C. tomokunii View in CoL .
Material examined. Type material: 1♂ Lectotype: Bao Ha, Tonkin ( Vietnam), 20.04.1924, leg. H. Stevens [ BMNH, NHMUK 010266912].
Other material: Total 6♂: 1♂ Mt. Tam Dao, Vinh Phu Province, northern Vietnam, 1994, leg. M. Hämäläinen [ RMNH]. 1♂ “Stream below Thac Bac” Tam Dao, Vinh Phu Province, northern Vietnam, 26.06.2008, leg. M. Hämäläinen [ RMNH]. 1♂ same locality, 28.06.2008, leg. M. Hämäläinen [ RMNH]. 3♂ “Rhododendron & Fivelakes trail” Bach Ma National Park, Thua Tien Hue Province, central Vietnam, 15– 18.06.2008, leg. M. Hämäläinen [ RMNH].
Description of the lectotype. Head ( Fig. 2 View FIGURE 2 A): Completely black except for diffuse greyish patches reaching out apically from the ocelli; typical postocular spots only just visible, the coloration faded away almost entirely. Prothorax ( Fig. 2 View FIGURE 2 B–C): All black, posterior lobe slightly raised.
Synthorax ( Fig. 2 View FIGURE 2 B–C): Black dorsally, with two big yellow markings ( Fig. 2 View FIGURE 2 B). Synthorax laterally black with two big yellow markings, the lower one covering most of the metepimeron, the upper one covering the posterior part of the metepisternum up to the metathoracic spiracle, dorsally reaching slightly onto the mesepisternum. A small but distinct black spot near the upper margin of the metepisternal yellow marking; mesepisternum black.
Wings ( Fig. 2 View FIGURE 2 G–H): Hyaline with black Pt, covering nearly two cells in Fw and Hw. 21 Px in Fw, 20 Px in Hw. RP 2 arising slightly proximal to Px 10 in Fw, between Px 7 and Px 8 in Hw. IR1 arises at Px 13 in Fw, and at Px 11 in Hw. IR2 arises slightly distal to subnodus in all wings.
Abdomen: Slender, black with whitish lateral spots on S3–6.
Anal appendages ( Fig. 2 View FIGURE 2 D–F): Paraprocts slightly overtopping cerci in length. Cerci with small, medially directed spine on upper inner border; followed dorsoapically by a rounded elevation, and with distinct ventromedial tooth arising subapically. This tooth is difficult to see in the lectotype, as the cerci are turned so that the tooth is rather directed inwards.
Genital ligula ( Fig. 5 View FIGURE 5 A–B, Supplementary Fig. 1 View FIGURE 1 ): First segment simple with distal bend; second segment curved with well-developed inner fold, without terminal fold; third segment flat, median part distinctly raised, with two recurved flagella arising medially from raised part, bordering first segment.
Measurements (mm): Lectotype: Total length: 49, Abd.: 42, Fw/Hw (left): 21.
Measurement ranges of the six studied specimen collected near the type locality: Total length: 55–61, Abd.: 47–52, Fw (left): 29–34, Hw (left): 29–34.
Variation. Head ( Fig. 3 View FIGURE 3 A): Specimens from near the type locality show more extensive whitish coloration reaching out from the lateral ocelli towards the antennal bases, which have a whitish base; postocular spots distinct, yellowish white.
Synthorax ( Fig. 3 View FIGURE 3 B–C): Lateral yellow markings of the specimens from near the type locality agree well with the lectotype, but there is great variation in the extent of the two dorsal, escutcheon-shaped spots. In some specimens they cover about one third of the dorsal part of the synthorax as in the lectotype; in other specimens the spots cover up to two thirds of the dorsal synthorax ( Fig. 3 View FIGURE 3 B–C). The coloration, described by Laidlaw (1932: 22) as “…citron or sulphur-yellow…” also varies in the specimen from the type locality; some specimen have citron markings as in the lectotype, while in others the markings are of a rather deep golden yellow color ( Fig. 3 View FIGURE 3 B–C).
Anal appendages ( Fig. 3 View FIGURE 3 D–F): In some of the other specimens examined, the anal appendages dried in another position than in the lectotype, so that the ventromedial tooth is directed straight downward and the small spine is directed rather obliquely inward ( Fig. 3 View FIGURE 3 D–F). Asahina (1997: 23) did not describe the anal appendages for C. tomokunii but mentioned that the superior appendages are “provided with inflated head…”. Depending on the position of these appendages, this impression may arise from the rounded dorsoapical elevation.
Genital ligula ( Fig. 5 View FIGURE 5 C–D, Supplementary Fig. 2 View FIGURE 2 ): All specimens from near the type locality with two small thin flaps arising laterally from raised median part of segment three, posterior of origin of flagella ( Fig. 1 View FIGURE 1 C, 5 C– D). Flaps missing in the lectotype.
Remarks. The specimens of Coeliccia scutellum studied show rather strong variation in coloration, size and shape of dorsal markings. In order to visualize this variability, we illustrate a specimen that is most different from the lectotype in all mentioned characters ( Fig. 3 View FIGURE 3 ). The genital ligula of all examined specimens, differs from the genital ligula of the lectotype in having two thin lateral flaps on segment three ( Fig. 1 View FIGURE 1 C, 5 C–D). The lectotype is the only specimen without flaps on the genital ligula, although the shape of the ligula is otherwise consistent with that found in the other specimens. Since there are no other structural differences between the lectotype and the other examined specimens, it seems possible that the flaps have eroded in the lectotype. Alternatively, within the 70 years that passed between the collection of the lectotype and the collection of the other specimens examined the genital ligula might have changed due to sexual selection or genetic drift. It seems also possible that there is variation in the shape of the genital ligula, with the lectotype without flaps representing the extreme end of the variability.
As the somatic and genital variability is strong between lectotype and all other examined specimens, we suggest that C. tomokunii is synonymous with C. scutellum . Investigating the variability in a long series of C. scutellum , in particular the assessment of whether there is continuous variation in flap size or bimodal distribution, would help to clarify the taxonomic status. We propose the following synonymy:
Coeliccia scutellum Laidlaw, 1932 View in CoL
Syn. Coeliccia tomokunii Asahina, 1997 View in CoL , syn. nov.
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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Coeliccia scutellum Laidlaw, 1932
Steinhoff, Philip O. M. & Uhl, Gabriele 2015 |
C. scutellum Laidlaw, 1932 ( Wilson & Reels 2001 )
Laidlaw, 1932 (Wilson & Reels 2001 |
Coeliccia tomokunii
Asahina 1997 |
Coeliccia tomokunii
Asahina 1997 |
Coeliccia scutellum
Laidlaw 1932 |