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New record of Juvenile Stethojulis trilineata (Perciformes: Labridae) from Korea, Revealed by Molecular Analysis
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ABSTRACT
New record of Juvenile Stethojulis trilineata (Perciformes: Labridae) from Korea, Revealed by Molecular Analysis
KEYWORD
Stethojulis trilineata , New record , Labridae , Korea , mtDNA COI
  • Introduction

    The family Labridae in the order Perciformes comprises 453 species and 68 genera worldwide (Nelson, 2006), with 20 species and 14 genera in Korea (Kim et al., 2005). This family is one of the most diverse groups of marine fishes, displaying various shapes, colors, and sizes (Nelson, 2006). Among them, the genus Stethojulis has a wide extended range from the Red Sea to Hawaii; it consists of 10 species worldwide (Randall, 2000), although only one species, S. interrupta, occurs in Korea. A juvenile color pattern that differs from that of the adult is present in some fish groups (Allen, 1991), and juveniles in most of the family Labridae differ in their color patterns from the adult (Mahon, 1994; Victor et al., 2001; Westneat, 2002). Thus, recent studies of juvenile identification have used both morphological descriptions and molecular methods (Chow et al., 2003; Li et al., 2006; Robertson et al., 2007; Victor et al., 2009; Kwun et al., 2012). In this study, we confirmed that a single specimen collected from Ulsan, Korea, was Stethojulis trilineata using molecular analyses, and we describe the species as the first record based on a specimen.

    Materials and Methods

    A single specimen of Stethojulis trilineata was collected from Ulsan, Korea on October 26, 2012, and was fixed in 99% ethanol. Counts and measurements followed Hubbs and Lagler (2004), using a vernier caliper to the nearest 0.1 mm. The vertebrae were counted from a radiograph (Softex HA-100; Softex, Tokyo, Japan). The specimen was deposited at the National Institute of Biological Resources (NIBR), Korea. Molecular identification of this specimen was performed using VF2 (5′-TCAACCAACCACAAAGACATTGGCAC-3′) and FishR2(5′-ACTTCAGGGTGACCGAAGAATCAGAA-3′) primers, which amplify the mitochondrial DNA cytochrome oxidase subunit I (COI) (Ward et al., 2005; Ivanova et al., 2007). Genomic DNA was extracted from eye using Chelex 100 resin (Bio-Rad, Hercules, CA, USA). A polymerase chain reaction (PCR) was performed in a total volume 50 μL containing DNA template 5 μL, dNTP 4 μL, 10x buffer 5 μL, Taq polymerase 0.5 μL, reverse primer 1 μL, forward primer 1 μL, and distilled water. PCR was conducted under the following conditions: initial denaturation for 1 min at 95℃, followed by 35 cycles of 1 min at 95℃ for denaturation, 1 min at 50℃ for annealing, and 1 min at 72℃ for extension, with a final extension at 72℃ for 5min. The PCR products were purified using ExoSAP-IT (United States Biochemical Corp., Cleveland, OH, USA). The DNA was sequenced using an ABI 3730XL sequencer and an ABI PRISM BigDye Terminator (ver. 3.0) Ready Reaction Cycle Sequencing Kit (Applied Biosystems, Foster City, USA). The nucleotide sequence was deposited in the DDBJ/EMBL/GenBank database (accession number: KF264566). The sequence was aligned with ClustalW (Thompson et al., 1994) in BioEdit (ver. 7) (Hall, 1999). The sequences of six Stethojulis species (S. albovittata, S.interrupta, S. trilineata, S. strigiventer, S. bandanensis, and S. balteata), from the National Center for Biological Information database were used for the sequence comparison. Genetic distances were calculated with the Kimura-2-parameter model (Kimura, 1980) in MEGA 5 (Tamura et al., 2011).

    Results and Discussion

      >  Stethojulis trilineata Bloch and Schneider, 1801 (Korean name: se-jul-mu-ji-gae-nol-rae-gi)

    Labrus trilineata Bloch and Schneider, 1801: 253 (type locality: Corimgo, Coromandel, India).

    Julis sebanus Valenciennes in Cuvier and Valenciennes, 1839: 474 (no locality).

    Julis (Halichoeres) phekadopleura Bleeker, 1849: 8 (type locality: Boleling, Bali).

    Halichoeres sebae Kner, 1860: 50 (no locality).

    Stethojulis phekadopleura Bleeker, 1862: 134 (type locality: Indonesia).

    Stethojulis filholi Sauvage, 1880: 225 (type locality: Fiji).

    Stethojulis trilineata: Bleeker, 1862: 131 (India); Günther, 1862: 140 (East Indian Archipelago); Masuda et al., 1984: 207 (Tokara Island and the Red Sea); Randall, 2000: 36 (Indo-South Pacific); Hutchins, 2001: 269 (Western Australia); Shimada, 2002: 984 (Japan); Adrim et al., 2004: 125 (Anambas, South China Sea); Motomura et al., 2010: 172 (Japan); Allen and Erdmann, 2012: 720 (Indo-Pacific).

      >  Material examined

    NIBR-P0000020417, 1 specimen, 23.6 mm in standard length (SL), Ulsan, Nasa-ri, 26 Oct, 2012, collected by Kwun

    [Table 1.] Comparison of meristic characters of Stethojulis trilineata

    label

    Comparison of meristic characters of Stethojulis trilineata

    HJ and Jang IC.

      >  Description

    Proportion as % SL: body depth 22.5; body width 10.6; head length 31.8; snout length 8.5; eye diameter 8.1; interorbital width 13.6; upper jaw length 4.2; predorsal length 32.6; prepelvic length 32.6; preanal length 55.5; base of dorsal spine length 17.8; base of dorsal ray length 25.8; pectoral fin length 14.4; pelvic fin length 11.0; caudal peduncle depth 12.3; caudal peduncle length 10.6.

    Counts are shown in Table 1. Body elongated, compressed, and moderately deep. Mouth small, terminal, and lips thin. The anterior ends of both jaws coincide well. A single row of small conical teeth on both jaws and the two front teeth are more developed than the others. Posterior tip of maxilla not reaching to the anterior margin of the eye. Dorsal margin of the head slightly sloping and single pair of nostrils located in front of the eyes. Body covered with large cycloid scales but head scaleless. Lateral line continuous, but tending sharply downward below the 8th dorsal fin ray to the straight caudal fin base. Anus located in middle of the body. Opercle large, and posterior margin of opercle beyond the origin of pectoral fin. Margin of opercle smooth, but with two small spines. Dorsal fin with no obvious notch between spinous and soft portions. Pectoral fins somewhat large and fan-shaped. Pelvic fin short and origin of the pelvic fin below posterior end of the base of the pectoral fin. Caudal fin slightly rounded.

      >  Coloration

    When fresh, the body and head are yellowish-green dorsally and pale green ventrally. A silver–white stripe extends from the front of the snout through the eye to the caudal peduncle, fading posteriorly. All fins are transparent, and dark spots occur between the 10th and 11th dorsal fin rays and caudal peduncle region. After fixation, the body and head are pale green, fading gradually ventrally. The body and head, except for the ventral part of the head and abdomen, have many small melanophores. Posterior to the opercle and on the cheek below the lower jaw are small dark spots. A stripe with small melanophores extends from the snout to the caudal peduncle. Small melanophores occur along the dorsal fin, pectoral fin, and caudal fin rays.

      >  Distribution

    Stethojulis trilineata is distributed in the Indo-Pacific (Randall, 2000), South China Sea (Adrim, 2004), Japan (Masuda et al., 1984; Shimada, 2002), and Korea (southern part of the East Sea, Ulsan; present study).

      >  Remarks

    The specimen collected from Ulsan belongs to the genus Stethojulis in having a continuous spinous and soft portion of the dorsal fin, a lateral line sharply bent but connected, a naked head, and XI dorsal fin spines (Table 1, Fig. 1). Compared with the original description, this specimen corresponds to S. trilineata in having a green body, scaleless head, XI dorsal fin spines, and 13 pectoral fin rays (Table 1). Based on comparisons with juveniles of S. trilineata reported by Randall (2000), the specimen (juvenile) in this study is similar in having dark spots between the 10th and 11th dorsal fin rays and a caudal peduncle region, and with small melanophores behind the opercle. To identify the species exactly, we analyzed the mitochondrial DNA COI gene, which indicated that the specimen’s DNA sequence almost corresponded to that of S. trilineata (d = 0.002–0.005) and differed slightly from that of S. interrupta (d = 0.020–0.023). Thus, this specimen was identified as S. trilineata based on molecular and morphological analyses. Although S. trilineata is morphologically similar to S. interrupta (also reported in Korea) in the number of its dorsal fin rays (S. trilineata IX, 11 vs. S. interrupta IX, 11–12) and pectoral fin rays (12–13 vs. 13, respectively) (Randall, 1986, 2000; Shimada, 2002; Kim et al., 2005; Allen and Erdmann, 2012), differences exist in the numbers of gill rakers (25–28 vs. 19–23, respectively), suborbital pores (8–12 vs. 6–9, respectively), dark spots in the caudal peduncle region (present only in females vs. absent in both males and females, respectively), and the last stripe starting from the snout (extends to the caudal peduncle vs interrupted on the anterior half of the body) (Westneat, 1999; Randall, 2000; Shimada, 2002; Allen and Erdmann, 2012). The juvenile of S. trilineata is also similar to that of S. interrupta in having a small dark spot posteriorly on the dorsal and anal fins near their bases, but the former is clearly distinguishable from the latter in having a narrow silver–white stripe extending from the frontof the snout to the caudal fin (vs. two narrow black stripes). Similarly, the juvenile of S. trilineata has a silver–white stripe, and not only has dark spots between the 10th and 11th dorsal fin rays and the caudal peduncle region, but also small dark spots on the posterior region of the opercle. These characteristics differ from those of juvenile S. strigiventer, which has a narrow white stripe from the front of the snout through the upper part of the eye and continuing to the upper caudal fin base, and a more irregular white stripe from the corner of the mouth through the lower part of the eye to the lower caudal fin base; S. albovittata, which has a small black spot near the base of the last membrane of the dorsal and anal fins; and S. balteata, which has two small spots at the base of the caudal fin, a smaller black spot midlaterally on the caudal peduncle, and a black spot rimmed with yellow posteriorly on the dorsal and anal fins (Randall and Kay, 1974; Randall, 2000).

    The family Labridae is one of the groups in which the color patterns of juveniles differ from the adult patterns, and members also display sexual dimorphism (Mahon, 1994; Victor et al., 2001; Westneat, 2002). Stethojulis trilineata also has dark spots on the dorsal fin rays and caudal peduncle, which disappear gradually as it grows, when three narrow stripes appear. Thus, further study is required to provide an exact morphological description of adult S. trilineata. We propose the new Korean name “Se-jul-mu-ji-gae-nol-rae-gi” for S. trilineata, based on its morphological characteristic of three narrow longitudinal rows on the body of the adult.

참고문헌
  • 1. Adrim M, Chen IS, Chen ZP, Lim KKP, Tan HH, Yosof Y, Jaafar Z. 2004 Marine fishes recorded from the Anambas and Natuna Islands, South China Sea. [Raffles Bull Zool Suppl] Vol.11 P.117-130 google
  • 2. Allen GR. 1991 Damselfishes of the World. google
  • 3. Allen GR, Erdmann MV. 2012 Reef Fishes of the East Indies. Vol. II. P.630-726 google
  • 4. Bleeker P. 1849 Bijdrage tot de kennis der ichthyologische fauna van het eiland Bali, met beschrijving van eenige nieuwe species. [Verh Batav Genoot Kunsten Wet] Vol.22 P.1-11 google
  • 5. Bleeker P. 1862 Atlas Ichthyologique des Indes Orientales Neerlandaises, publie sous les auspices du Gouvernement colonial neerlandais. Vol. 1. Scaroideset Labroides. google
  • 6. Bloch ME, Schneider JG. 1801 M. E. Blochii, Systema Ichthyologiae iconibus cx illustratum. Post obitum auctoris opus inchoatum absolvit, correxit, interpolavit Jo. Gottlob Schneider, Saxo. Berolini. google
  • 7. Chow S, Nohara K, Tanabe T, Itoh T, Tsuji S, Nishikawa Y, Uyeyanagi S, Uchikawa K. 2003 Genetic and morphological identification of larval and small juvenile tunas (Pisces: Scombridae) caught by a mid-water trawl in the western Pacific. [Bull Fish Res Agency] Vol.8 P.1-14 google
  • 8. Cuvier G, Valenciennes A. 1839 Histoire naturelle des poissons. Tome treizieme. Livre seizieme. Des Labroides. Vol. 13 P.1-505 google
  • 9. Gunther A. 1862 Catalogue of the Acanthopterygii Pharyngognathi and Anacanthini in the collection of the British Museum. google
  • 10. Hall TA. 1999 BioEdit: a user-friendly biological sequence alignment editor and analysis program for Windows 95/98/NT. [Nucleic Acids Symp Ser] Vol.41 P.95-98 google
  • 11. Hubbs CL, Lagler KF. Fishes of the Great Lakes Region. Revised ed. P.US google
  • 12. Hutchins JB. 2001 Biodiversity of shallow reef fish assemblages in Western Australia using a rapid censusing technique. [Rec West Aust Mus] Vol.20 P.247-270 google
  • 13. Ivanova NV, Zemlak TS, Hanner RH, Hebert PDN. 2007 Universal primer cocktails for fish DNA barcoding. [Mol Ecol Notes] Vol.7 P.544-548 google cross ref
  • 14. Kim IS, Choi Y, Lee CL, Lee YJ, Kim BJ, Kim JH. 2005 Illustrated book of Korean Fishes. google
  • 15. Kimura M. 1980 A simple method for estimating evolutionary rates of base substitutions through comparative studies of nucleotide sequences. [J Mol Evol] Vol.16 P.111-120 google cross ref
  • 16. Kner R 1860 Zur Charakateristik und Systematik der Labroiden. [Sitzungsber Kais Akad Wiss Wien] Vol.40 P.41-57 google
  • 17. Kwun HJ, Kim JK, Kwun SM. 2012 First record of bluespot mullet, Moolgarda seheli (Mugiliformes: Mugilidae) from Jeju Island, Korea. [Korean J Ichthyol] Vol.24 P.297-301 google
  • 18. Li Z, Nishimoto MM, Love MS, Gharrett AJ. 2006 Comparing the identification of southern California juvenile rockfishes (genus Sebastes spp.) by restriction site analysis of the mitochondrial ND3/ND4 region and by morphological characteristics. [Fish Bull] Vol.104 P.376-382 google
  • 19. Mahon JL. 1994 Advantage of flexible juvenile coloration in two species of Labroides (Pisces: Labridae). [Copeia] Vol.1994 P.520-524 google cross ref
  • 20. Masuda H, Amaoka K, Araga C, Uyeno T, Yoshino T. 1984 The Fishes of the Japanese Archipelago. google
  • 21. Motomura H, Kuriiwa K, Katayama E, Senou H, Ogihara G, Meguro M, Matsunuma M, Takata Y. 2010 Annotated checklist of marine and estuarine fishes of Yaku-shima Island, Kagoshima, Southern Japan. In: Fishes of Yaku-shima Island?A World Heritage Island in the Osumi Group, Kagoshima Prefecture, southern Japan. P.65-247 google
  • 22. Nelson JS. 2006 Fishes of the World. google
  • 23. Randall JE. 1986 Family No. 220: Labridae. In: Smiths’ Sea Fishes. Smith MM and Heemstra PC, eds. P.683-706 google
  • 24. Randall JE. 2000 Revision of the Indo-Pacific labrid fishes of the genus Stethojulis, with descriptions of two new species. [Indo-Pac Fish] Vol.31 P.1-42 google
  • 25. Randall JE, Kay JC. 1974 Stethojulis axillaris, a junior synonym of the Hawaiian labrid fish Stethojulis balteata, with a key to the species of the genus. [Pac Sci] Vol.28 P.101-107 google
  • 26. Robertson MD, Ovenden JR, Barker SC. 2007 Identification of small juvenile scombrids from northwest tropical Australia using mitochondrial DNA cytochrome b sequences. [Ichthyol Res] Vol.54 P.246-252 google cross ref
  • 27. Sauvage HE. 1880 Description de quelques poissons de la collection du Museum d’Histoire Naturelle. [Bull Soc Philomath Paris] Vol.4 P.220-228 google
  • 28. Schultz LP. 1943 Fishes of the Phoenix and Samoan Islands collected in 1939 during the expedition of the U. S. S. “Bushnell”. [Bull US Natl Mus] Vol.180 P.1-316 google cross ref
  • 29. Shimada K. 2002 Labridae. In: Fishes of Japan with Pictorial Keys to the Species. Nakabo, T, ed. English ed. P.969-1013 google
  • 30. Tamura K, Peterson D, Peterson N, Stecher G, Nei M, Kumar S. 2011 MEGA5: molecular evolutionary genetics analysis using maximum likelihood, evolutionary distance, and maximum parsimony methods. [Mol Biol Evol] Vol.28 P.2731-2739 google cross ref
  • 31. Thompson JD, Higgins DG, Gibson TJ. 1994 CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. [Nucleic Acids Res] Vol.22 P.4673-4680 google cross ref
  • 32. Victor BC, Wellington GM, Robertson DR, Ruttenberg BI. 2001 The effect of the El Nino-Southern oscillation event on the distribution of reef-associated labrid fishes in the eastern Pacific Ocean. [Bull Mar Sci] Vol.69 P.279-288 google
  • 33. Victor BC, Hanner R, Shivji M, Hyde J, Caldow C 2009 Identification of the larval and juvenile stages of the Cubera Snapper, Lutjanus cyanopterus, using DNA barcoding. [Zootaxa] Vol.2215 P.24-36 google
  • 34. Ward RD, Zemlac TS, Innes BH, Last PR, Hebert PDN. 2005 DNA barcoding Australia’s fish species. [Philos Trans R Soc Lond B Biol Sci] Vol.360 P.1847-1857 google cross ref
  • 35. Westneat MW. 1999 The Living Marine Resources of the Western Central Pacific: FAO Species Identification Sheets for Fishery Purposes. P.3381-3467 google
  • 36. Westneat MW. 2002 Family Labridae. In: FAO species identification sheets for fishery purposes. The Living Marine Resources of the Western Central Atlantic. Carpenter KE, ed. P.1701-1723 google
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  • [ Table 1. ]  Comparison of meristic characters of Stethojulis trilineata
    Comparison of meristic characters of Stethojulis trilineata
  • [ Fig. 1. ]  Stethojulis trilineata, NIBR-P0000020417, 23.6 mm standard length, collected from Ulsan. (A) Fresh specimen, (B) preserved specimen.
    Stethojulis trilineata, NIBR-P0000020417, 23.6 mm standard length, collected from Ulsan. (A) Fresh specimen, (B) preserved specimen.
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