Cephalothrix suni Chernyshev & Polyakova 2021, sp. nov.

• Main Authors: Chernyshev, Alexei V., Polyakova, Neonila E.
• Format: Text
• Language: unknown
• Published: Zenodo 2021
• Subjects: Biodiversity; Taxonomy; Animalia; Nemertea; Palaeonemertea; Cephalothricidae; Cephalothrix; Cephalothrix suni; Arctic; Antarctic; Queensland; Antarc*
• Online Access: https://dx.doi.org/10.5281/zenodo.4455270; https://zenodo.org/record/4455270

Cephalothrix suni sp. nov. (Figs 1A, B; 2 A-I; 3A-I) urn:lsid:zoobank.org:act: 602F23A5-7D8A-47BF-AB88-10D40D72C6BA syn. Cephalothrix sp. VIE: Chen et al. , 2010, tab. 2, N 21. Cephalothrix suni : Chernyshev, 2016, p. 288 ( nomen nudum ) Type material. Holotype No. 40373 (MIMB), slides with transverse sectionas, Nam Du Island (09°43′ N, 104°23′ E), South China Sea, Vietnam, May 15, 2010, intertidal, calcareous red algae, collected by A. V. Chernyshev. Paratype No. 40374 (MIMB), Van Phong Bay (12°34′ N, 109°24′ E), South China Sea, Vietnam, January 13, 2005, intertidal, calcareous red algae, collected by A. V. Chernyshev. Other material examined . Three specimens, Van Phong Bay (12°33′ N, 109°23′ E), South China Sea, Vietnam, January 18, 2005, intertidal, calcareous red algae, collected by A. V. Chernyshev. GenBank accession numbers . Holotype (KU 840272 – Sundberg et al . 2016; see Table 2), paratype (GU726621 – Chen et al . 2010). Etymology. The specific epithet honors Prof. Sun Shichun (Ocean University of China). Description. External features . Body 50–80 mm long but less than 1 mm wide. Bluntly rounded head not narrower than trunk; anterior tip of head red (holotype) or orange (paratype), demarcated posteriorly by white band (Fig 1). Eyes absent. Background colour pale yellowish; dark pigment present on ventral side only. Small round mouth rimmed by brown ring with thicker anterior and posterior margins; two thin brown longitudinal stripes connected with in posterior part of the ring and extend to gut region (Fig. 1). Gut region with transverse dark drown bands; very thin transverse ring (epidermal furrow?) runs through each band. Brown spots also arranged between bands, sometimes forming irregular longitudinal stripes. Worms crawl on the dorsal side of their bodies, with the ventral side facing up. Internal morphology . Body wall: E = 20–26 µm, D = 5–8 µm, OCM = 4–7 µm, LM = 18–35 µm; outer part of LM and inner part of split OCM present (Figs 2B; 3 C-E;); in cerebral and foregut regions, crisscrossed DM located between dermis and OCM (Fig. 2D, F); in foregut region, dorsal muscular cross present between OCM and rhynchocoel wall (Fig. 2F); very thin ICM adjoins ventral wall of anterior foregut portion and connected with musculature of lateral blood vessel (Fig. 2A, B, E); posterior foregut portion lacks ICM (Fig. 2C). Longitudinal muscle plate between rhynchocoel and digestive tract present (Fig. 2F). Proboscis musculature consists of OCM, DM, LM, and very thin ICM (Fig. 2G); large pseudocnidae 5.6–6.5 × 1.9–2.5 µm, small pseudocnidae 3.3–4.1 × 0.9–1.3 µm (Fig. 2H); proboscis epithelium with longer (23–26 µm) and shorter (14–17 µm) collars of sensory cells (Fig. 2I). Ratio of brain–head tip to brain–mouth distances 1: 1.4 (based on transverse sections). Gut epithelium with dark pigment (Fig. 3I). Four cephalic nerves present (Fig. 3A). Single large median ventral nerve extends backwards from ventral brain commissure (Fig. 3C) and forms two buccal nerves immediately in front of mouth (Fig. 3D); two buccal nerves (Fig. 3E, F) join together (Fig. 3G) and become invisible immediately behind mouth (Fig. 3H). Dorsal nerve located between DM and OCM (Fig. 2F). Blood system typical for cephalotrichids; rhynchocoel vessel of type A according to Kajihara’s (2010) classification (Fig. 3B). Mushroom-like excretory organs present. Comparison . Almost all species of the genus Cephalothrix s.l. have more or less uniformly coloured body without any pattern, except for Cephalothrix queenslandica which, the same as the new species, possesses a distinct colour pattern consisting of transverse brown bands. However, according to the original description (Sundberg et al. 2003), Cephalothrix queenslandica has a brown anterior tip (in contrast to orange or red tip in C. suni ), transverse brown bands on the dorsal body surface (in contrast to the bands on the ventral surface in C. suni ), and two cephalic nerves (in contrast to four ones in C. suni ). The uncorrected p -distance between the 18S rRNA sequences (no other sequences for C. queenslandica are known) of C . queenslandica and C. suni constitutes 0.5%. For comparison, the p -distance between the 18S rRNA sequences of Cephalothrix hongkongiensis Sundberg, Gibson & Olsson, 2003 and C. suni is 0.2%. Geographical and ecological distribution . South China Sea, South Vietnam, Van Phong Bay, and off Nam Du Island; intertidal zone, among calcareous red algae. Remarks . C. suni is apparently the most common species of Cephalothrix in coastal waters off Vietnam. In addition, another Cephalothrix species (Chernyshev 2016; GenBank accession no. MW118027) has been found in coastal waters off Vietnam (Cu Lao Cham Islands). The latter is similar to the undescribed species C. fasciculus sensu Leasi & Norenburg 2014 from Belize (GenBank accession no. KM083814.1). Phylogenetic analysis . According to a phylogenetic analysis, the genus Cephalothrix is monophyletic and includes three highly supported clades: Cephalothrix sensu Chernyshev & Kajihara 2019, Procephalothrix sensu Chernyshev & Kajihara 2019, and ‘interstitial cephalotrichids’ with two undescribed species. The new species belongs to clade Procephalothrix , where Cephalothrix suni , C. rufifrons (Johnston, 1837), C. hongkongiensis, Cephalothrix mokievskii Korotkevitsch, 1982 (see Chernyshev 2020), and C. simula (Iwata, 1952) form a highly supported subclade of species with orange, red, or dark yellow anterior tip. This subclade is sister to subclade with two undescribed Cephalothrix from Arctic and Antarctic waters. Recently, Chernyshev & Kajihara (2019) have shown that the name Procephalothrix may be ‘resurrected’ for the clade that contains Cephalothrix filiformis (Johnston, 1828) (type species of Procephalothrix ) and other species with the outer part of LM located between the lateral nerve cord and OCM. : Published as part of Chernyshev, Alexei V. & Polyakova, Neonila E., 2021, An integrative description of a new Cephalothrix species (Nemertea: Palaeonemertea) from the South China Sea, pp. 584-594 in Zootaxa 4908 (4) on pages 588-591, DOI: 10.11646/zootaxa.4908.4.10, http://zenodo.org/record/4447032 : {"references": ["Chen, H., Strand, M., Norenburg, J. L., Sun, S., Kajihara, H., Chernyshev, A. V., Maslakova, S. A. & Sundberg P. (2010) Statistical Parsimony Networks and Species Assemblages in Cephalotrichid Nemerteans (Nemertea). PLoS One, 5 (9), e 12885. https: // doi. org / 10.1371 / journal. pone. 0012885", "Chernyshev, A. V. (2016) Nemerteans of the coastal waters of Vietnam. In: Adrianov, A. V. & Lutaenko, K. A. (Eds.), Biodiversity of the Western Part of the South China Sea. Dalnauka, Vladivostok, pp. 279 - 314.", "Sundberg, P., Kvist, S. & Strand, M. (2016) Evaluating the utility of single-locus DNA barcoding for the identification of ribbon worms (phylum Nemertea). PLoS ONE 11: e 0155541.", "Sundberg, P., Gibson, R. & Olsson, U. (2003) Phylogenetic analysis of a group of palaeonemerteans (Nemertea) including two new species from Queensland and the Great Barrier Reef, Australia. Zoologica Scripta, 32, 279 - 296. https: // doi. org / 10.1046 / j. 1463 - 6409.2002.00032. x", "Leasi, F. & Norenburg, J. L. (2014) The necessity of DNA taxonomy to reveal cryptic diversity and spatial distribution of meiofauna, with a focus on Nemertea. PLoS ONE, 9 (8), e 104385. https: // doi. org / 10.1371 / journal. pone. 0104385", "Chernyshev, A. V. & Kajihara, H. (2019) Comparative muscular morphology in Archinemertea (Nemertea: Palaeonemertea). Zoomorphology, 138, 193 - 207. https: // doi. org / 10.1007 / s 00435 - 019 - 00440 - w"]}