Metaruncina antoni, Chernyshev, 2021
publication ID |
https://doi.org/ 10.11646/zootaxa.4974.1.12 |
DOI |
https://doi.org/10.5281/zenodo.4771976 |
persistent identifier |
https://treatment.plazi.org/id/D77287ED-FF9D-FFA6-FF08-FA16A78E4E8F |
treatment provided by |
Plazi |
scientific name |
Metaruncina antoni |
status |
sp. nov. |
Metaruncina antoni sp. nov.
( Figs 1 View FIGURE 1 , 2A–E View FIGURE 2 )
urn:lsid:zoobank.org:act:49C23EB5-1B4A-4F26-B066-B03F4EA724AA
Type material. Holotype No. 40037 ( MIMB), Tho Chu Island (09°19′ N, 103°30′ E), South China Sea, Vietnam, May 13, 2010, intertidal, dead corals and calcareous red algae, collected by A. V. Chernyshev during the expedition aboard the R / V “Akademik Oparin” GoogleMaps . Paratype No. 40038 ( MIMB), collected with holotype GoogleMaps . Paratypes (4 specimens) No. 40039 ( MIMB), Van Phong Bay (12°39′ N, 109°20′ E), South China Sea, Vietnam, May 21, 2010, intertidal, dead corals, and calcareous red algae, collected by A. V. Chernyshev GoogleMaps .
Other material examined. 1 juv. specimen, Cu Lao Re Island , (15°23′ N, 109°05′ E), South China Sea, Vietnam, May 25, 2007, intertidal, among Halimeda sp. , collected by A. V. Chernyshev during the expedition aboard the R / V “Akademik Oparin” GoogleMaps ; 3 specimens, No. 40039a ( MIMB), collected along with paratypes (all specimens were dissected) .
Etymology. The species is named in memory of Dr. Anton Chichvarkhin (1975–2020) for his contribution to the investigation of marine heterobranch mollusks.
Description. Living animals 2–4.5 mm long, with elongated oval notum and anteriorly truncated head. Larger specimens (3–4.5 mm long) have yellowish brown notum with two dark brown (to almost black) longitudinal, slightly irregular, and sometimes intermittent stripes ( Fig. 1A, B, F View FIGURE 1 ). Dark brown margin of notum thickens at posterior part of notum, and laterally at the level of eyes visible through notum ( Fig. 1A, C, D, F View FIGURE 1 ). Two large, rounded, dark spots located near anterior edge of notum ( Fig. 1 A–D View FIGURE 1 ). Dark digestive gland shows through integument. Foot slightly lighter on dorsal surface, with small brown speckles against yellowish brown background; longitudinal medial aggregation of dark pigment expands towards notum; dark speckles fewer on ventral surface of foot ( Fig. 1E View FIGURE 1 ); dark margin on foot absent. Gill large, protruding from under notum, with 4–5 pinnae on each side, dark coloured especially on pinnae edges ( Fig. 1B, F View FIGURE 1 ). Specimens 2–2.5 mm long are lighter in colour, with irregular longitudinal stripes markedly intermittent. Shell translucent, barely visible through integument, elongated, tapering to posterior end ( Fig. 1B, F View FIGURE 1 ), 240–260 µm long and 96–110 µm wide ( Fig. 2C View FIGURE 2 ).
Jaws consist of numerous scale-like elements 5–6 µm wide, anterior elements with 6–7 denticles on anterior margin ( Fig. 2A View FIGURE 2 ). Buccal apparatus with brown pigment. Radula of “juvenile” type, asymmetrical, 3 × 0.R.1 and one more row 1.R.1 (?0.R.2) ( Fig. 2A, B View FIGURE 2 ); rachidian teeth bear slightly discernible serration on cutting edge ( Fig. 2B View FIGURE 2 ). In mature specimens, gizzard plates 100–205 µm long, with 7–9 V-shaped ridges ( Fig. 2D View FIGURE 2 ). Male copulatory apparatus without distinct penial papilla, slander seminal vesicle ca. 480 µm long, prostatic part ca. 600 µm long ( Fig. 2E View FIGURE 2 ).
Remarks. The new species is placed in the genus Metaruncina by presenting rudimentary juvenile-type radula, single gill, internal posterior plate-like shell, and four gizzard plates. Metaruncina antoni sp. nov. is distinguished from the known two Metaruncina species in body colour: M. setoensis has uniformly black notum with white shell while M. nhatrangensis bears five dorsal black brown longitudinal stripes.
Geographical distribution and habitat. South China Sea, South Vietnam, Van Phong Bay, Tho Chu Island, and Cu Lao Re Island. In the intertidal zone, among calcareous red and green algae.
Discussion. The monotypic genus Metaruncina was established by Baba (1967) for Runcina setoensis Baba, 1954 . The main distinguishing feature of the new genus was a strongly reduced radula, different from the typical serial radula of runcinids. Such interpretation of Metaruncina radula is still accepted by many authors. It should be noted that the socalled “metamorphosis of radula” ( Thompson & Brodie 1988; Schmekel & Cappellato 2001, 2002), where the “juvenile” (provisional) radula is replaced by the “adult” (definitive) one, has been described from some of runcinids ( Thompson & Brodie 1988; Chernyshev 1998; Schmekel & Cappellato 2001, 2002). Some juvenile individuals may have both juvenile and definitive radula ( Thompson & Brodie 1988; Schmekel & Cappellato 2002; Chernyshev 1998).
A comparison of the provisional radula of Runcinida marisae Chernyshev, 1998 with the drawings of the radula of Metaruncina setoensis in the Baba’s work (1967) gave the author the idea that Metaruncina in the adult stage retains the “juvenile” radula, while the typical serial radula is not formed ( Chernyshev 1998). Further studies on the radula in Metaruncina nhatrangensis confirmed its similarity to the provisional radula of hatched juvenile specimens of Runcinida marisae ( Fig. 2F View FIGURE 2 ) ( Chernyshev 2005). Thus, the radula in Metaruncina is non-homologous to the definitive radula in other runcinids and is rather a “juvenile” radula retained in the adult state, i.e., it represents an example of paedomorphosis. Besides species of the genus Metaruncina , a “juvenile” radula was described from Runcina avellana Schmekel & Cappellato, 2001 ( Schmekel & Cappellato 2001) and species of the genus Fofinha Moro & Ortea, 2015 ( Moro & Ortea 2015; Ortea & Moro 2020). However, it should be considered that Runcina avellana has a very small body size and was described without information about the copulative apparatus, and, therefore, it is possible that the studied specimens were juvenile individuals having no definitive radula ( Schmekel & Cappellato 2001). Nevertheless, Ortea (2013) transferred Runcina avellana to the genus Pseudoilbia M. C. Miller & Rudman, 1968 . Being described from a single specimen, Pseudoilbia lineata M. C. Miller & Rudman, 1968 has a serial asymmetric radula with the formula 35–39 × 2.0.2 ( Miller & Rudman 1968), and such radula is not provisional. For this reason, examination the Mediterranean Runcina species is required to clarify the generic placement of R. avellana .
MIMB |
Museum of the Institute of Marine Biology |
V |
Royal British Columbia Museum - Herbarium |
R |
Departamento de Geologia, Universidad de Chile |
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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