taxonID	type	description	language	source
03DCE14DFF9AFFC5E99446CEFD7BFE49.taxon	description	Figures 1 ‒ 3, 5 ‒ 6; Tables 1 ‒ 3	en	Tang, Chi-Ngai, Matsunuma, Mizuki (2022): Redescription of Chelidoperca barazeri, with a revised key and literature review to species of Chelidoperca in Taiwan (Perciformes: Serranidae). Zootaxa 5189 (1): 204-221, DOI: https://doi.org/10.11646/zootaxa.5189.1.19
03DCE14DFF9AFFC5E99446CEFD7BFE49.taxon	materials_examined	Type series. NTUM 15639, holotype, 32.2 mm SL; NTUM 15635, paratype, 32.0 mm SL, sta. CP 4262, 2 ˚ 4 ’ S, 151 ˚ 07 ’ E, 150 – 160 m. Gazelle Channel, New Ireland, Bismarck Sea, R / V Alis, French beam trawl, MADEEP expedition, 25 Apr. 2014. Non-type specimens. All from southwestern Taiwan: KAUM – I. 115150, 65.2 mm SL, 115151, 45.6 mm SL, Ke-tzu-liao, Kaoshiung, southwestern Taiwan, coll. by K. Koeda et al., bottom trawl, 8 May 2018; KUN-P 55609, 57.8 mm SL, 55610, 40.9 mm SL, 55611, 59.0 mm SL, off Kaoshiung, southwestern Taiwan, coll. by H. - C. Ho, bottom trawl, 16 Sept. 2019; NMMB-P 35231 (CO 1: ON 797433), 53.1 mm SL, 35232 (CO 1: ON 797434), 50.8 mm SL, Ke-tzu-liao, Kaoshiung, southwestern Taiwan, ca. 100 m, bottom-trawl, 24 Jan. 2021, coll. by C. - N. Tang; NMMB-P 35233 (CO 1: ON 797435), 67.7 mm SL, 35234 (CO 1: ON 797436), 66.1 mm SL, 35235 (CO 1: ON 797437), 64.4 mm SL, 35236 (CO 1: ON 797438), 59.6 mm SL, 35237 (CO 1: ON 797439), 54.1 mm SL; Ke-tzu-liao, Kaoshiung, southwestern Taiwan, ca. 100 m, bottom-trawl, 31 Jan. 2021, coll. by C. - N. Tang.	en	Tang, Chi-Ngai, Matsunuma, Mizuki (2022): Redescription of Chelidoperca barazeri, with a revised key and literature review to species of Chelidoperca in Taiwan (Perciformes: Serranidae). Zootaxa 5189 (1): 204-221, DOI: https://doi.org/10.11646/zootaxa.5189.1.19
03DCE14DFF9AFFC5E99446CEFD7BFE49.taxon	diagnosis	Diagnosis. A species of Chelidoperca distinguished from congeners by the following combination of characters: three scale rows between lateral line and base of 6 th dorsal-fin spine (two full-sized plus a dorsalmost half-sized scales); pored lateral-line scales 34 ‒ 37 (modally 36); scale rows in longitudinal series 35 – 39 (modally 38); developed gill rakers 1 ‒ 2 + 7 ‒ 8 (modally 2 + 7); cheek scale rows 4 – 7 (modally 5); dentary surface of lower jaw naked; interorbital region with a single row of cycloid scales extend to or slightly beyond the mid-orbit level; outermost row of teeth of the upper jaw enlarged, antrorse and caniniform; outermost row of teeth of the lower jaw at the lateral side near symphysis with ca. 3 ‒ 4 enlarged antrorse canines, innermost row of teeth enlarged and caniniform; penultimate and the last dorsal- and anal-fin rays in adult not elongated; a red ocellus on opercular membrane between the spines; soft dorsal fin with series of large yellow spots; anal fin with a yellow margin; caudal fin with yellow spots along the basal-half median fin rays; and the presence of a faint and discontinuous stripe formed by clusters of melanophores along the mid-lateral body when preserved.	en	Tang, Chi-Ngai, Matsunuma, Mizuki (2022): Redescription of Chelidoperca barazeri, with a revised key and literature review to species of Chelidoperca in Taiwan (Perciformes: Serranidae). Zootaxa 5189 (1): 204-221, DOI: https://doi.org/10.11646/zootaxa.5189.1.19
03DCE14DFF9AFFC5E99446CEFD7BFE49.taxon	description	Description. The following values are provided for the holotype with the paratype and non-types in parentheses. Dorsal-fin elements X, 10; anal-fin elements III, 6; caudal fin slightly rounded, total caudal-fin rays - (30 ‒ 33), principal rays - (9 + 8), branched rays - (8 + 7); upper / lower procurrent caudal-fin rays - / - (6 – 9 / 6 ‒ 7). Scale rows above lateral line to the dorsal-fin origin 3 (3 ‒ 4); scale rows below lateral line 9 (9 – 10); cheek scale rows 4 (4 – 7); predorsal-fin scale rows 7 (6 ‒ 8); circumpeduncular scales 17 (17 ‒ 18). First gill arch with 17 (15 ‒ 18) total rakers, including 3 (3 – 5) (rudimentary) + 2 (1 ‒ 2) (developed) rakers on the upper limb and 7 (7 – 8) (developed) + 5 (2 – 5) (rudimentary) rakers on the lower limb. Pseudobranchial filaments 12 (11 – 18). Branchiostegal rays 7. Vertebrae 10 (precaudal) + 14 (caudal) = 24; supraneurals 3; formula for the configuration of supraneural spines and anterior dorsal pterygiophores 0 / 0 / 0 + 2 / 1 + 1 / 1; ribs present on the 3 rd vertebrate to the 10 th. Terminal dorsal pterygiophore in interneural space 16; terminal anal pterygiophore in interhaemal space 4. TABLE 1. Morphometric data and count of head serrae of Chelidoperca barazeri and two similar species. Means of head serrae were recorded to nearest integer. Data for comparison were adopted from Matsunuma et al. (2018). Data sources: A. Present study; B. Matsunuma et al. (2018). HT = holotype; D = dorsal; A = anal. ...... Continued on the next page Body elongated, cylindrical in section anteriorly, gradually becoming compressed posteriorly. Body depth and width 24.8 % (22.1 – 26.9 %) and 18.6 % (16.6 – 20.1 %) of SL, respectively. Head moderately large, its length 38.8 % (37.1 – 38.8 %) of SL, upper profile not steep. Snout moderately blunt, anterior margin forms an angle ca. 40 ‒ 50 ° with the upper jaw, its length 17.6 % (15.6 – 21.3 %) of HL, shorter than the eye diameter. Eye moderately large, its diameter 35.2 % (29.9 – 36.6 %) of HL; bony interorbital width narrow, 6.4 % (5.9 – 7.5 %) of HL. Mouth large and slightly oblique, the upper-jaw length 43.2 % (42.7 – 46.7 %) of HL. Postorbital length 50.4 % (49.5 – 53.4 %) of HL; predorsal length 38.2 % (35.3 – 38.2 %) of SL; preanal length 61.5 % (60.0 – 63.1 %) of SL; prepelvic length 32.6 % (30.7 – 34.7 %) of SL; caudal peduncle relatively long, length 63.6 % (57.5 – 68.6 %) of HL, the least caudal peduncle depth 32.0 % (27.8 – 33.0 %) of HL. Dorsal-fin origin above a vertical through pectoral-fin base, the first spine shortest, 16.4 % (11.8 – 19.4 %) of HL; fourth spine longest, 44.5 % (38.9 – 48.5 %) of HL, length of spine gradually reducing after the fourth; the ninth spine 22.6 % (14.9 – 23.0 %) of HL, the last (tenth) spine longer than the ninth, 23.2 % (19.6 – 25.6 %) of HL; all soft rays branched, generally subequal in length, not elongated or filamentous, the penultimate (ninth) ray longest, its length 50.4 % (40.0 – 62.5 %) of HL. Anal-fin origin below the base of the second dorsal-fin ray; the third spine longest, its length 27.5 % (16.7 – 27.8 %) of HL; all soft rays branched, not elongated, the penultimate (fifth) ray longest, its length 49.3 % (42.2 – 57.3 %) of HL. Pectoral fin with uppermost two rays unbranched, remaining rays branched, its posterior tip do not reach the level of anal-fin origin; its length 72.0 % (61.4 – 72.0 %) of HL. Pelvic-fin origin below the pectoral-fin base; the spine covered with skin, its length 39.3 % (27.8 – 40.5 %) of HL; all soft rays branched, the second longest and elongate, 76.0 % (61.3 – 76.0 %) of HL, expanded distally, its tip pointed, reaching the anus when appressed. Caudal fin slightly rounded, its length 52.0 % (52.0 – 75.0 %) of HL. Anterior nostrils situated at the middle of snout, its opening with a small rounded flap rising from the posterior rim (or short membranous tube); posterior nostril an elliptical opening at anterior border of eye. Opercle with two flat prominent spines, the upper spine slightly longer than the lower spine, interopercular-spine width 12.8 % (12.8 ‒ 16.3 %) of HL; posterior edge to the angle of preopercle serrated, with 19 / 21 (19 – 39) well-developed serrae; upper distal edge of interopercle serrated, with 5 / 4 (4 – 18, one non-type without serrae on one side) weak, not welldeveloped serrae; lower distal edge of subopercle serrated, with 13 / 11 (10 – 25) weak serrae; posttemporal with a small bony crest with 2 / 2 (2 – 4) serrae tips at the beginning of the lateral line. Maxilla with a low lateral ridge along the median level; ventral part of maxilla with a low skin fold extended from the premaxilla; lower jaw slightly protruding beyond the upper jaw when the mouth is closed. Bands of small conical teeth and enlarged canines on both jaws, vomer and palatine bands, teeth bands tend to be broader in larger specimens. The anterior (broadest) portion of tooth band on the upper jaw at symphysis with ca. 4 – 7 rows of small, sharp-tipped conical teeth, progressively longer towards the inner rows, the band becoming narrower posteriorly; outermost row of upper jaw with enlarged antrorse canines (Fig. 3 D); anterior (broadest) portion of lower jaw at symphysis with ca. 3 ‒ 4 rows of sharp-tipped conical teeth, progressively longer towards the inner rows, the outermost row of teeth at the symphysis stout and enlarged, the band becoming narrower posteriorly; the outermost row near symphysis at lateral side with ca. 3 ‒ 4 enlarged antrorse canines (Fig. 3 E), and enlarged canines along the innermost row. Vomer with a V-shaped band consisting ca. 3 ‒ 5 rows of small conical teeth at broadest part, a few enlarged canines at posterior end of each sides. Palatine band consisting ca. 2 ‒ 4 rows of small sharp-tipped conical teeth, the innermost row often enlarged. Body generally covered with ctenoid scales, except for several regions with cycloid scales. Uppermost row of body scales along the dorsal-fin base about half size of the scales on body. Lateral line complete, slightly arched over pectoral fin and gradually descending, terminating at caudal-fin base. Pored lateral-line scales 35 (34 – 37). Scale rows in longitudinal series 37 (35 – 39). Pectoral fin with a scaly basal sheath. Scales absent on all rays and membranes of dorsal, anal and pelvic fins. Caudal fin with scaly basal sheath with ctenoid scales, scales extended to and covering one-third to half of the area from the fin base, scales on caudal fin ctenoid. Head generally covered with both ctenoid and cycloid scales; snout (including infraorbital), maxilla and ventral surface of dentary naked; ventral surface of the angular covered with ca. 2 ‒ 4 (more rows in larger non-type specimen, fewer in small specimens) rows of cycloid scales, not extended onto the dentary; cheek (preopercle) possesses both cycloid and ctenoid scales (larger non-type specimens with more ctenoid scales on the upper two-third area); scales on interopercle cycloid; scales on subopercle and opercle ctenoid; scales on interopercular membrane cycloid; interorbital with a single row of cycloid scale reaching or slightly anterior to the mid-orbit level (some specimens were judged by scale pockets due to scale loss). Prepelvic area possess mainly cycloid scales, except scale in the vicinity of pelvic-fin base with few and weak ctenii. A pair of interorbital canals with numerous small pores running along outer margin of interorbital region, diverging outward anteriorly, and reaching between anterior and posterior nasal pores. Lower jaw with four, nonpaired large sensory pores on each side (Fig. 3 C), the anteriormost pore near symphysis, followed by two pores along the sensory canal of the dentary surface, the last one located between the junction of dentary and angular. Fresh coloration. Based on adult specimens from Taiwan (Fig. 1 A ‒ C). Body pinkish red, becoming paler ventrally. Upper body darker, scales above lateral line with dark brown edges. Several small shiny white spots scattering along and above the lateral line. A faint reddish stripe (ca. 1.5 scale in width) running horizontally along the body axis. Chest shiny white. Lateral body with ca. 9 whitish or iridescent vertical rectangular bars along the ventral profile. Head (snout and jaws) generally reddish pink. Premaxilla with a white spot at the anterior part, becoming pale yellow posteriorly. Maxilla pale red. Lower jaw with a white spot near the symphysis (present on both sides). A small iridescent white stripe extends posteroventrally from the posterior edge of maxilla to the anteroventral margin of preopercle. Iris yellow with dusky reddish pigments. Upper rim of eye reddish. Cheek and opercle not uniformly red, region posterior to the maxilla sometimes more reddish (may varies due to condition of specimens). Opercular membrane between the spines with a distinct red spot (red ocellus), with a translucent white margin. Spinous dorsal-fin membrane translucent white, with several irregular yellow spots, the distal margin of membrane yellow. A small group of dark reddish spot (ca. 4 ‒ 6) on the basal half of the 4 th to 6 th spine. Soft dorsalfin membrane translucent white, with 2 ‒ 3 rows of large yellow spot along the rays, upper distal margin translucent white. Anal fin translucent white with broad yellow margin, distal tip of soft rays sometimes reddish. Membrane between the branches of the last anal-fin ray creamy white, a pale yellow spot sometimes present on the mid-way. Caudal fin translucent white, becoming translucent yellow posteriorly. Two yellow spots near the base of the middle caudal-fin rays, a short vertical yellow bar at middle of the fin, several dusky reddish spots along dorsal and ventral margin. Pectoral fin yellow hyaline, an obvious reddish spot near the base of the middle rays. Pelvic fin with a creamy white anterior margin, remainder translucent yellow, distal tip of soft rays sometimes reddish. Preserved coloration. Body pale white in general; upper body dusky, posterior field of scales with dark crescent in larger specimens (Fig. 2 A). A faint, discontinuous stripe formed by clusters of melanophores along the mid lateral body (more obvious in smaller specimens, see Fig. 2 A ‒ B). Snout with a faint cluster of melanophores on each side. Dorsal fin with several irregularly clusters of melanophores along the base, spine and rays. Anal fin translucent white. Caudal fin dusky near the base. Pectoral fin base and distal tip of anal fin slightly dusky.	en	Tang, Chi-Ngai, Matsunuma, Mizuki (2022): Redescription of Chelidoperca barazeri, with a revised key and literature review to species of Chelidoperca in Taiwan (Perciformes: Serranidae). Zootaxa 5189 (1): 204-221, DOI: https://doi.org/10.11646/zootaxa.5189.1.19
03DCE14DFF9AFFC5E99446CEFD7BFE49.taxon	distribution	Distribution. Chelidoperca barazeri has only been recorded in its type locality, the Gazelle Channel of Bismarck Sea, Papua New Guinea (Lee et al., 2019), and newly recognized in southwestern Taiwan. It is predicted that C. barazeri is a widespread species in the western Pacific.	en	Tang, Chi-Ngai, Matsunuma, Mizuki (2022): Redescription of Chelidoperca barazeri, with a revised key and literature review to species of Chelidoperca in Taiwan (Perciformes: Serranidae). Zootaxa 5189 (1): 204-221, DOI: https://doi.org/10.11646/zootaxa.5189.1.19
03DCE14DFF9AFFC5E99446CEFD7BFE49.taxon	biology_ecology	Ecology. Chelidoperca barazeri is a relatively shallow water species compare to its congeners. It was trawled from seamount and bands at depth 150 – 160 m in its type locality (Lee et al., 2019). In Taiwan, it is captured by bottom-trawl off southwestern Taiwan, the depth of the trawl operation is assumed to be rubble sandy bottom (topology of seafloor unknown) at depth ca. 100 m, judging from others by-catch species [e. g., Neomerinthe erostris (Alcock, 1896), Scorpaena miostoma Günther, 1877]. Size. Chelidoperca barazeri is recognized as a relatively small species. The largest specimen examined is 67.7 mm SL, which is a mature male individual (NMMB-P 35233, Fig. 1 A) with developed testes, several smaller specimens are mature females with ripe ovaries (NMMB-P 35231, Fig. 1 C; NMMB-P 35237).	en	Tang, Chi-Ngai, Matsunuma, Mizuki (2022): Redescription of Chelidoperca barazeri, with a revised key and literature review to species of Chelidoperca in Taiwan (Perciformes: Serranidae). Zootaxa 5189 (1): 204-221, DOI: https://doi.org/10.11646/zootaxa.5189.1.19
03DCE14DFF9AFFC5E99446CEFD7BFE49.taxon	discussion	Remarks. Phylogenetic analysis based on the COI dataset (Fig. 5) highly support the identification of C. barazeri. The K 2 P genetic distance within C. barazeri from Taiwan and its type locality (northern Papua Guinea) is relatively small, ranging from 0.0 ‒ 0.2 % within 9 specimens, compare to the mean interspecific distances ranging from 9.2 ‒ 16.9 % calculated from the same dataset. This result is also expected at the range of intraspecific variation (Ward et al., 2005; Holmes et al., 2009). In morphology, no significant difference was observed between the types and newly collected non-types in this study. In addition, C. barazeri is sister to C. tosaensis (Fig. 4) with medium support; their genetic distances are ranging from 8.8 ‒ 10.0 %. Compare to another morphologically similar species, C. stella, their genetic distances are ranging from 11.6 ‒ 12.9 %. The fresh coloration of specimens of C. barazeri from type locality (Fig. 1 D) and Taiwan (Fig. 1 A ‒ C) are similar in general, but different in a few details. Types of C. barazeri possess four irregular dark pinkish red bands extend from dorsal profile to mid-body, each with longitudinally rectangular reddish blotches, and an oblique red stripe extended from infraorbital to the anteroventral margin of the opercle. These two characters are not obvious in the Taiwanese specimens. However, the differences in coloration may due to geographical or ontogenetic variation, or even the condition of the fresh specimens. Preserved coloration of types and Taiwanese specimens without distinctive difference, all these specimens possess a discontinuous line on mid lateral body formed by clusters of melanophores, fainter in larger specimens (Fig. 2).	en	Tang, Chi-Ngai, Matsunuma, Mizuki (2022): Redescription of Chelidoperca barazeri, with a revised key and literature review to species of Chelidoperca in Taiwan (Perciformes: Serranidae). Zootaxa 5189 (1): 204-221, DOI: https://doi.org/10.11646/zootaxa.5189.1.19
03DCE14DFF96FFC7E9944459FAB3FD64.taxon	discussion	Remarks. The specimens of C. tosaensis reported by Koeda & Ho (2019) were re-identified as C. barazeri by the authors. The record of C. tosaensis should be removed from the ichthyofauna of Taiwan at present. However, judging from the current distribution of C. tosaensis, from southern Japan, to Philippines and Papua New Guinea (Matsunuma et al., 2018; Lee et al., 2019), it is possible that C. tosaensis occurred in Taiwan as well.	en	Tang, Chi-Ngai, Matsunuma, Mizuki (2022): Redescription of Chelidoperca barazeri, with a revised key and literature review to species of Chelidoperca in Taiwan (Perciformes: Serranidae). Zootaxa 5189 (1): 204-221, DOI: https://doi.org/10.11646/zootaxa.5189.1.19
03DCE14DFF96FFC7E99445A1FABCFEFA.taxon	description	To summarize, 6 species of Chelidoperca were confirmed occurring in the Taiwanese water by literature survey. A list of records and a diagnostic key of Chelidoperca species in Taiwan were provided with comments.	en	Tang, Chi-Ngai, Matsunuma, Mizuki (2022): Redescription of Chelidoperca barazeri, with a revised key and literature review to species of Chelidoperca in Taiwan (Perciformes: Serranidae). Zootaxa 5189 (1): 204-221, DOI: https://doi.org/10.11646/zootaxa.5189.1.19
03DCE14DFF96FFC7E99447E7FCD3FCBC.taxon	discussion	Remarks. A new species described from southwestern Taiwan recently. A relatively rare species in Taiwanese water, no specimens were further collected after the description.	en	Tang, Chi-Ngai, Matsunuma, Mizuki (2022): Redescription of Chelidoperca barazeri, with a revised key and literature review to species of Chelidoperca in Taiwan (Perciformes: Serranidae). Zootaxa 5189 (1): 204-221, DOI: https://doi.org/10.11646/zootaxa.5189.1.19
03DCE14DFF96FFC7E994469FFB98FB30.taxon	discussion	Remarks. Shen (1984) reported Chorististium lunulatum (= Liopropoma lunulatum) from Taiwan. However, the figure has clear diagnostic characters of C. hirundinacea and is thus re-identified as C. hirundinacea. This is one of two species that commonly collected from southwestern and northeastern Taiwan.	en	Tang, Chi-Ngai, Matsunuma, Mizuki (2022): Redescription of Chelidoperca barazeri, with a revised key and literature review to species of Chelidoperca in Taiwan (Perciformes: Serranidae). Zootaxa 5189 (1): 204-221, DOI: https://doi.org/10.11646/zootaxa.5189.1.19
03DCE14DFF96FFC7E9944013FBF4F9C2.taxon	discussion	Remarks. This is one of two species that commonly collected from around Taiwan.	en	Tang, Chi-Ngai, Matsunuma, Mizuki (2022): Redescription of Chelidoperca barazeri, with a revised key and literature review to species of Chelidoperca in Taiwan (Perciformes: Serranidae). Zootaxa 5189 (1): 204-221, DOI: https://doi.org/10.11646/zootaxa.5189.1.19
03DCE14DFF96FFC7E994434EFE3DF86D.taxon	discussion	Remarks. This species is collected only from off southwestern Taiwan. Matsunuma et al. (2019) reported 3 specimens (NMMB-P 21104, 22803, 23108) collected from off Dong-gang, Kaoshiung and Tainan, southwestern Taiwan which represented the first record of Taiwan. In this study, we collected and examined 7 additional specimens from off southwestern Taiwan.	en	Tang, Chi-Ngai, Matsunuma, Mizuki (2022): Redescription of Chelidoperca barazeri, with a revised key and literature review to species of Chelidoperca in Taiwan (Perciformes: Serranidae). Zootaxa 5189 (1): 204-221, DOI: https://doi.org/10.11646/zootaxa.5189.1.19
03DCE14DFF97FFC6E99445A1FE3DFE4C.taxon	discussion	Remarks. Matsunuma et al. (2018) reported 2 specimens (NMMB-P 22749) collected from off Kaoshiung, southwestern Taiwan, which represented the first record of Taiwan. In this study, we collected 11 additional specimens from this region. This species occasionally occurs as bycatch from the bottom-trawling fisheries from southwestern Taiwan.	en	Tang, Chi-Ngai, Matsunuma, Mizuki (2022): Redescription of Chelidoperca barazeri, with a revised key and literature review to species of Chelidoperca in Taiwan (Perciformes: Serranidae). Zootaxa 5189 (1): 204-221, DOI: https://doi.org/10.11646/zootaxa.5189.1.19
