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Redescription of Parapercis macrophthalma (Pietschmann, 1911) and description of a new species of Parapercis (Pisces: Pinguipedidae) from Taiwan

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Abstract

Parapercis macrophthalina is confirmed as a valid species and redescribed on the basis of the holotype and other specimens collected from the type locality, Taiwan, and Japan. It is morphologically similar to P. muronis Tanaka, 1918, but differs in having five vertical transverse bars that extend well below the lateral line versus five oblique transverse bars, with the third to fifth bars ending on or above the lateral line. A new species is also described on the basis of a specimen collected from southwestern Taiwan. It is distinct in having numerous pores interconnected by canals on the head, forming 10 vertical or oblique rows on the cheek and opercular apparatus, predorsal scales extending to the level of the posterior margin of the eye, four dorsal-fin spines, six oblique bars laterally on the body, and a combination of other characters. A key to species of Parapercis with narrow transverse bars on the upper body is provided.
Accepted by J. Sparks: 10 Jan. 2013; published: 6 Mar. 2013
ZOOTAXA
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http://dx.doi.org/10.11646/zootaxa.3620.2.5
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Redescription of Parapercis macrophthalma (Pietschmann, 1911) and description
of a new species of Parapercis (Pisces: Pinguipedidae) from Taiwan
HSUAN-CHING HO1,3 & JEFFREY W. JOHNSON2
1National Museum of Marine Biology & Aquarium; Institute of Marine Biodiversity and Evolutionary Biology, National Dong Hwa
University; no. 2, Houwan Rd., Checheng, Pingtung 944, Taiwan. E-mail: ogcoho@gmail.com
2Ichthyology, Queensland Museum, PO Box 3300, South Brisbane, Q 4101, Australia. E-mail: jeff.johnson@qm.qld.gov.au
3Corresponding author.
Abstract
Parapercis macrophthalma is confirmed as a valid species and redescribed on the basis of the holotype and other
specimens collected from the type locality, Taiwan, and Japan. It is morphologically similar to P. muronis Tanaka, 1918,
but differs in having five vertical transverse bars that extend well below the lateral line versus five oblique transverse bars,
with the third to fifth bars ending on or above the lateral line. A new species is also described on the basis of a specimen
collected from southwestern Taiwan. It is distinct in having numerous pores interconnected by canals on the head, forming
10 vertical or oblique rows on the cheek and opercular apparatus, predorsal scales extending to the level of the posterior
margin of the eye, four dorsal-fin spines, six oblique bars laterally on the body, and a combination of other characters. A
key to species of Parapercis with narrow transverse bars on the upper body is provided.
Key words: Teleostei, taxonomy, Parapercis macrophthalma, Parapercis moki n. sp., new species, Taiwan
Introduction
Pietschmann (1911) described Neopercis macrophthalma on the basis of a single specimen 127 mm in total length
collected from Taiwan (Fig. 1A). Cantwell (1964) placed it in Parapercis Bleeker, 1863, but with a doubtful status.
Gloerfelt-Tarp & Kailola (1984) recognized it as a valid species, based on a 92 mm SL voucher specimen from
Western Australia; however that record is based on an undescribed species (J. Johnson, unpub. data). Johnson
(2006) described Parapercis sexlorata from eastern Australia and compared it to P. macrophthalma which brought
the first author’s attention of the presence of the Taiwanese holotype.
In Taiwan, P. muronis (Tanaka, 1918) has been recorded for several decades (Chen, 1969; Shen, 1984a, b;
Chen & Yu, 1986; Shen et al., 1993), whereas P. macrophthalma has never been mentioned, probably due to the
close similarity of the two species. Johnson (2006) outlined the common features of the species, such as five dark
transverse bars on the upper body, the presence of palatine teeth, and similar body shape and most meristic values;
however characters that differentiate these two species were not provided.
In order to verify the two species mentioned above, a survey of the literature and examination of specimens of
both species was conducted. This revealed that records of P. muronis from Taiwan and Japan were often confused
with or misidentified as P. macrophthalma.
Furthermore, a single specimen with similar appearance to P. muronis was found in the Pisces collection of
National Museum of Marine Biology and Aquarium (NMMB-P) during our investigations. The specimen has
several unique characters and is not referable to any currently recognized species. The absence of any additional
specimens in collections throughout the region indicate that the species is rare. Hence, although represented by
only one specimen, we herein describe it as a new species.
HO & JOHNSON
274 · Zootaxa 3620 (2) © 2013 Magnolia Press
Methods and material
Type specimens for this study are housed at National Museum of Marine Biology & Aquarium, Pingtung, Taiwan
(NMMB-P) and the Humboldt University, Berlin (ZMB). Methods for taking measurements and counts followed
Randall et al. (2008), except for snout length which is measured as the flat horizontal distance between the tip of
the snout and the anterior margin of the eye. Other specimens examined are deposited in NMMB-P, Biodiversity
Research Center, Academia Sinica, Taipei, Taiwan (ASIZP), National Taiwan University, Taipei, Taiwan (NTUM),
Faculty of Science, Kochi University, Kochi, Japan (BSKU), National Museum of Nature and Science, Tsukuba,
Japan (NSMT-P), CSIRO Marine and Atmospheric Research, Hobart, Australia (CSIRO) and Queensland
Museum, Brisbane, Australia (QM). Abbreviations of institutes followed Fricke and Eschmeyer (2012). The
proportional and meristic values provided below are the value of the holotype, followed by the range of all other
specimens in parentheses, if different.
Results
Parapercis macrophthalma (Pietschmann, 1911)
English name: Narrow barred grubfish
Figs. 1A–C, Tables 1–2
Neopercis macrophthalma Pietschmann, 1911:431, fig. 1 (original description; type locality: Taiwan).
Parapercis macrophthalma (Pietschmann): Cantwell, 1964: 245 (new combination, with doubtful status); Johnson, 2006: 55.
Ho and Shao, 2011: tab. 1; ?Department of Fisheries Malaysia, 2009: 82.
Parapercis muronis (non Tanaka, 1918): Masuda et al, 1984: pl. 260, fig. E; Shen, 1984a: 115, pl. 115, fig. 37-12a, c (in part);
Shen, 1984b: 376; ?Chen and Yu, 1986: 694; Shen et al., 1993: 488, pl.164-4.
Parapercis sp.: Shinohara in Okamura and Amaoka, 1997:553, fig. 7.
Parapercis sp. 2: Shimada in Nakabo, 2002: 1064, 1586.
Material examined. Holotype: ZMB 16160 (108.3 mm SL), Takao [= Kaohsiung], SW. Taiwan, coll. K. A.
Haberer. Non-type: Tai w an : ASIZP 61408 (1, 111.6 mm), Audi, Taipei, bottom trawl, 200 m, 15 Nov. 2000, coll.
C.-H. Wu. ASIZP 61551 (1, 90.6 mm), Tashi, Yi-lan, bottom trawl, 100 m, 17 Jul. 2000, coll. C.-H. Wu. ASIZP
62349 (1, 87.0 mm), Fonggang, Pingtung, bottom trawl, 200 m, 1 Mar. 2001, coll. J.-H. Wu. CSIRO H.6293-08 (1,
88.2 mm), Tashi fish market, near Yi-Lan, Taiwan, coll. W. White, 22 May 2005. NMMB-P0492 (1, 103.5 mm),
Tungkang, Pingtung, coll. H.-K. Mok. NMMB-P1692 (1, 102.1 mm), Tongkang, Pingtung, 7 Feb. 1985.
NMMB-P2453 (1, 112.6 mm), Kaohsiung, 9 Apr. 2002, coll. J.-P. Chen. NTUM 4116 (1, 106.1 mm), Kaohsiung,
28 Mar. 1980. NTUM 4468 (1, 113.6 mm), Chung-chou, Kaohsiung, 26 Feb. 1984. NTUM 5613 (4, 98.2–111.6
mm) Chung-chou, Kaohsiung, 24 July 1979. NTUM 5614 (4, 88.9–102.6 mm), Chung-chou, Kaohsiung, 31 Oct.
1982. QM I.37582 (1, 107.2 mm), Donggang, Pingtung, Taiwan, 24 Jul. 2005. Japan: BSKU 44047 (1, 116.2
mm), Mimase fish market, Kochi city (offshore trawl in Tosa Bay), Japan, 2 Oct. 1987. BSKU 44049 (1, 117.5
mm), Mimase fish market (offshore trawl in Tosa Bay), Kochi, Japan, 2 Oct. 1987. BSKU 44053 (1, 112.1 mm),
Mimase fish market (offshore trawl in Tosa Bay), Kochi, Japan, 2 Oct. 1987. BSKU 44054 (1, 110.3 mm), Mimase
fish market (offshore trawl in Tosa Bay), Kochi, Japan, 2 Oct. 1987. BSKU 44069 (1, 95.6 mm), Mimase fish
market (offshore trawl in Tosa Bay), Kochi, Japan, 2 Oct. 1987. BSKU 44183 (1, 69.3 mm), Tosa Bay, Japan, 33º
17.79’N, 133º 42.17’E to 33º 17.25’N, 133º 41.07’E, beam trawl 189–191 m, 28 Oct. 1987. BSKU 44968 (1, 60.6
mm), Tosa Bay, Japan, 33º 17.38’N, 133º 42.58’E to 33º 16.81’N, 133º 41.53’E, beam trawl, 183–188 m, 8 Aug
1988. BSKU 44969 (1, 95.6 mm), Tosa Bay, Japan, 33º 17.38’N, 133º 42.58’E to 33º 16.81’N, 133º 41.53’E, beam
trawl, 183–188 m, 8 Aug. 1988. BSKU 44971 (1, 79.6 mm), Tosa Bay, Japan, 33º 17.38’N, 133º 42.58’E to 33º
16.81’N, 133º 41.53’E, beam trawl, 183–188 m, 8 Aug. 1988. BSKU 45287 (1, 105.9 mm), Mimase fish market,
Kochi city (offshore trawl in Tosa Bay), Japan, 22 Oct. 1988.
Diagnosis. A species of Parapercis with five vertical transverse bars on upper body, each extending laterally
to lower two-thirds of body and a combination of the following characters: 5 dorsal-fin spines, becoming
progressively longer posteriorly, with last spine entirely connected to first dorsal-fin ray by membrane; dorsal-fin
soft rays usually 23; anal fin usually with 1 spine and 19 soft rays; entire body covered by ctenoid scales, except for
Zootaxa 3620 (2) © 2013 Magnolia Press · 275
A NEW PARAPERCIS AND REDESCRIPTION OF P. MACROPHTHALMA
FIGURE 1. A–C. Parapercis macrophthalma (Pietschmann, 1911). A. Holotype of Neopercis macrophthalma, ZMB 16160,
holotype, 108.3 mm SL, Takao [Kaohsiung], Taiwan. B. NMMB-P17746, fresh condition,1 of 3, 120 mm SL, NE Taiwan,
photo by H-C Ho. C. NMMB-P2453, 112.6 mm SL, preserved condition. D. Parapercis muronis (Tanaka, 1918), BSKU 36380,
fresh condition, 123.8 mm SL, Tosa Bay, photo by BSKU.
HO & JOHNSON
276 · Zootaxa 3620 (2) © 2013 Magnolia Press
those on chest; predorsal scales extending forward to vertical from preopercle; generally 4 pairs of canine teeth
anteriorly in lower jaw; palatine with two rows of stout teeth, those on outer row larger than inner; vomer with
triangular patch of stout teeth; appressed pelvic fin not reaching anus.
TABLE 1. Morphometric data, expressed in percentage of standard length, for Parapercis macrophthalma, P. muronis and P.
moki n. sp.
Description. Morphometric and meristic data are provided in Tables 1–2. Dorsal-fin rays V, 24 (V, 22–24;
usually 23); anal-fin rays I, 19 (I, 18–19; usually 19); all dorsal and anal soft rays branched, the last to base;
pectoral-fin rays 20/21 (19–21; modally 20, rarely 21), branched except uppermost; pelvic-fin rays I, 5; principal
caudal-fin rays 9 (upper)+ 8 (lower)=17; upper procurrent caudal-fin rays 7–8; lower procurrent caudal-fin rays
5–6 (both upper and lower procurrent caudal-fin rays unclear in holotype); lateral-line scales 53 (51–56, not
including 2 or 3 smaller pored scales on base of caudal fin); scales above first lateral-line scale to origin of dorsal
fin 5.5; scales above highest part of lateral line to base of dorsal fin 4.5; scales below lateral line posteroventrally to
P. macrophthalma P. m uro ni s P. m ok i n. sp.
Holotype Non-type Non-type Holotype
ZMB 16160 N=23 N=13 NMMB–P 0892
SL (mm) 108.3 90.4–112.6 80.6–126.7 104.4
Morphometrics Mean (Range) SD Mean (Range) SD
Body depth 19.5 19.3 (16.1–21.2) 1.4 19.8 (19.0–20.8) 0.6 17.7
Body width 17.9 19.4 (17.2–22.2) 1.4 18.7 (17.4–20.4) 1.0 18.8
Head length 29.5 27.9 (26.1–29.5) 1.2 26.7 (23.6–28.2) 1.1 28.4
Snout length 5.9 6.0 (5.0–6.6) 0.5 6.4 (5.7–6.7) 0.3 6.8
Orbital diameter 10.6 10.3 (9.0–11.1) 0.7 9.2 (8.1–10.5) 0.9 9.2
Interorbital width 3.2 2.8 (2.0–3.5) 0.5 2.7 (1.8–3.2) 0.5 1.6
Preorbital depth 3. 3.3 (2.9–3.8) 0.3 3.4 (3.0–3.7) 0.2
Upper jaw length 12.2 11.5 (10.0–12.4) 0.5 11.5 (10.8–12.5) 0.5 11.6
Predorsal length 32.1 31.1 (30.2–33.2) 0.8 29.4 (28.0–31.2) 1.1 30.7
Preanal length 49.6 48.2 (44.9–51.1) 1.5 47.2 (45.9–49.2) 0.9 48.5
Prepelvic length 27.7 26.3 (24.6–28.7) 1.1 25.5 (24.5–26.7) 0.7 27.3
Caudal-peduncle depth 10.2 9.4 (8.2–10.5) 0.6 9.9 (9.1–10.2) 0.3 8.1
Caudal-peduncle length 8.1 7.8 (6.9–8.7) 0.5 8.2 (7.3–8.8) 0.4 7.7
Dorsal-fin base 61.9 62.8 (60.3–65.6) 1.6 64.0 (62.5–65.0) 0.8 63.9
First dorsal-fin spine 2.1 (1.1–3.0) 0.5 2.3 (1.6–2.8) 0.4 5.3
Second dorsal-fin spine 4.1 3.7 (2.5–5.1) 0.7 4.0 (2.7–5.1) 0.6 6.8
Third dorsal-fin spine 5.0 5.3 (4.0–7.0) 0.8 5.4 (4.7–5.9) 0.4 7.5
Fourth dorsal-fin spine 5.9 6.1 (5.1–7.2) 0.6 6.3 (5.5–6.8) 0.4 8.6
Fifth dorsal-fin spine 6.3 6.8 (5.5–8.3) 0.8 7.1 (6.4–7.6) 0.4 Absent
Longest dorsal-fin ray 15.2 14.3 (11.6–15.5) 1.1 14.9 (13.9–16.0) 0.7 14.0
Anal-fin base 43.9 44.5 (42.5–46.8) 1.1 44.9 (40.4–46.5) 1.7 45.0
Anal-fin spine length 4.2 4.0 (3.0–4.9) 0.6 4.4 (3.5–5.3) 0.5 4.0
Longest anal-fin ray 13.1 12.8 (10.9–14.5) 0.7 12.7 (11.7–14.2) 0.7 11.7
Caudal-fin length 19.5 (18.5–21.1) 0.7 19.2 (18.1–20.6) 0.8 17.7
Pectoral-fin length 24.5 22.6 (20.4–24.5) 1.1 22.8 (20.3–24.8) 1.2 21.6
Pelvic-fin length 22.5 21.9 (19.4–24.0) 1.2 21.1 (19.0–23.1) 1.4 19.4
Zootaxa 3620 (2) © 2013 Magnolia Press · 277
A NEW PARAPERCIS AND REDESCRIPTION OF P. MACROPHTHALMA
origin of anal fin about 14 (14–16); median predorsal scales 9; circumpeduncular scales 22 (22–23) (mainly 23);
gill rakers 5+8 =13 (4–6 + 8–10 = 12–16), pseudobranchial filaments 15 (14–22); branchiostegal rays 6; vertebrae
10 + 22 (9–10 + 22 = 31–32).
TABLE 2. Frequency distribution of selected meristic data for P. macrophthalma and P. m uron is. Counts for both left and right
pectoral-fin rays are included separately. * denotes holotype.
Body depth 5.1 (4.7–6.2) times in SL, 1.5 (1.3–1.8) in HL; body nearly cylindrical anteriorly, the width 5.6
(4.5–5.8) in SL, 1.6 (1.2–1.6) in HL, strongly compressed posteriorly; head relatively globular, its length 3.4
(3.4–3.8) in SL; ventral part of head, chest and abdomen slightly convex; snout relatively short and pointed, its
length 5.0 (4.0–5.4) in HL; eye relatively large, orbital diameter 2.8 (2.5–3.0) in HL; interorbital space flat, the
least fleshy width 9.2 (7.7–14.4) in HL; caudal-peduncle depth 2.9 (2.6–3.5) in HL; caudal-peduncle length 3.6
(3.1–4.1) in HL.
Mouth large, maxilla nearly reaching a vertical through anterior half of eye, upper-jaw length 2.4 (2.2–2.9) in
HL; mouth oblique, forming an angle of about 20° to horizontal axis of body, both jaw equally terminate; upper jaw
with outer row of 22/24 (19-28) conical teeth that curve medially and posteriorly, anterior 8 (6–8) increasingly
larger and more strongly recurved, remaining teeth in outer row on side of jaw decreasing in length; broad band of
villiform teeth medial to canines in about 6 rows at front of upper jaw, gradually narrowing posteriorly to a narrow
band in about 2–3 irregular rows; front of lower jaw with 3 (4; rarely 3) pairs of recurved canine teeth, all about
equal in size (some specimens including holotype may have lost canine teeth and failed to regrow them, but no
vacant tooth sockets were observed in these specimens); band of about 8 rows of villiform teeth medial to canines
at front of lower jaw, medial row continuing laterally in jaw posterior to last canine as row of 8 (7–8) increasingly
larger and more strongly recurved teeth (last 3-4 of these distinctly enlarged), followed by a single row of small
teeth to end of jaw; vomer with stout conical teeth forming a triangular patch of about 3 rows, those in anterior row
of 7 (7-8) teeth largest; palatine teeth usually in 2 distinct rows, outer row with 6/7 (6–8) teeth and the inner row
with 4/5 (4–5) slightly smaller teeth; lips smooth, their inner surface with large fleshy papillae that interdigitate
with anterior teeth; tongue broadly rounded, reaching forward to posterior vomerine teeth.
Gill membranes free from isthmus, with a broad transverse free fold. Gill rakers short and spinous, longest
about 1/3 length of longest gill filaments. Nostrils small, anterior nostril tube-like, in front of center of eye (viewed
from side), a little more than half way to groove at edge of upper lip, with pointed posterior flap that reaches
posterior nostril when laid back; posterior nostril dorsoposterior to anterior nostril, ovate with slight rim.
Pores of cephalic sensory system with row of 3 large pores above maxilla; 1 pore between both nostrils and 1
below anterior nostril; 4 pores on either side of space between posterior nostril to anterior interorbital space;
numerous pores connected by canals under the skin on posterior interorbital space and occiput; 1 series continuing
to posteroventral margin of eye along the upper margin of cheek scales, 1 series continuing to above the free
margin of preopercle, and a third series continuing to anterior end of lateral line on body; 2 rows of pores along the
inner margin of preopercle, outer row with 6 larger pores and inner row with 7 smaller pores, continuing to a series
of 4 large pores on mandibule; a pair of large pores at front of chin (mainly based on NMMB-P2453, 112.6 mm
SL).Opercle with single sharp spine, at about same level as ventral edge of pupil (when viewed from side); margin
of subopercle smooth except for 3 (3-6) blunt, close-set serrae on a small bony prominence on upper edge;
Lateral-line scales Pectoral-fin rays
n51 52 53 54 55 56 n18 19 20 21
P. macrophthalma 28 2 8 10* 4 2 2 28 21 33* 2*
P. m uro ni s 14 1 3 2 2 6 13 415 7 –
Gill rakers
Upper limb Lower limb Total
n 4 5 6 8 9 10 11 12 13 14 15 16 17
P. macrophthalma 26 915* 23* 18 5–18* 13 3 1 –
P. m uro ni s 14 11 3 – 8 4 2 – – 7 4 2 1
HO & JOHNSON
278 · Zootaxa 3620 (2) © 2013 Magnolia Press
preopercle broadly rounded, its free edge smooth except for slight indentation at each pore site, extending from
level of ventral edge of orbit downward and forward to slightly in front of vertical at posterior edge of orbit.
Scales strongly ctenoid and imbricate in entire body, except for those on chest which are cycloid or weakly
ctenoid; no scales on dorsal, anal, or pelvic fins; progressively smaller scales extending out on basal portion of
caudal fin for at least 2/3 length of fin; predorsal scales extending forward to, or slightly anterior to, a vertical from
hind margin of preopercle; lateral line broadly arched over pectoral fin, then gradually slanting to straight
midlateral portion on about posterior fourth of lateral body.
Origin of dorsal fin over third to fourth lateral-line scale, predorsal length 3.1 (3.0–3.3) in SL, slightly larger
than head length; 1st dorsal-fin spine relatively short, 9.5–26.7 (broken in holotype) in HL; 2nd dorsal-fin spine 7.2
(5.6–11.1) in HL; 3rd dorsal-fin spine 5.9 (4.1–7.2) in HL; 4th dorsal-fin spine longest, 5.0 (3.8–5.6) in HL; 5th
dorsal-fin spine 4.7 (3.4–5.0) in HL, entirely attached to 1st soft ray by membrane; last second dorsal soft ray
longest, 1.9 (1.7–2.5) in HL; origin of anal fin below base of 4th dorsal soft ray, preanal length 2.0 (2.0–2.2) in SL;
anal-fin spine 7.0 (5.3–9.7) in HL; last second anal soft ray longest, 2.3 (1.9–2.6) in HL; caudal fin rounded,
without prolongation on upper lobe; total fin length 4.7–5.4 in SL, 1.3–1.6 in HL (caudal fin damaged in holotype,
so only data from non-types) ; pectoral fins broadly rounded when spread, tenth ray longest, 4.1 (4.1–4.6) in SL,
1.2 (1.1–1.4) in HL; origin of pelvic fins anterior to pectoral fin origin, below base of exposed part of opercular
spine, prepelvic length 3.6 (3.5–4.1) in SL, 1.1 (1.0–1.1) in HL; pelvic fin relatively short, reaches anus to origin of
anal fin, fourth pelvic-fin ray longest, 4.4 (4.3–5.1) in SL, 1.3 (1.2–1.5) in HL.
Color when fresh (Fig. 1B). Body pale reddish above, grading to white ventrally, vivid white between pectoral
fin and pelvic fin; snout and upper jaw bright red; five vertical transverse bars distributed evenly on lateral body,
each with a solid black lower portion extending to about 2/3 of lower body, all well below the lateral line; dorsal fin
yellow, its posterior portion with some alternating yellow and blue oblique stripes; anal fin yellow; pelvic fins
reddish yellow with a large black patch on inner surface; caudal fin reddish yellow with some alternating yellow
and blue stripes; a brownish spot usually present on upper caudal fin base, between fourth to ninth rays.
Color in alcohol (Fig. 1C). Uniformly brownish yellow, with five vertical transverse bars, each with pale grey
upper part and solid black lower part; first bar at spinous dorsal fin, extending ventrally to above the upper pectoral
fin base; the other four distributed evenly along the body from the soft dorsal fin base, each extending ventrally to
a horizontal from lower 1/3 of the pectoral fin base, second bar extends about 5 horizontal scale rows below lateral
line, third bar about 4 scale rows below, fourth and fifth bars about 2.5 (2–3) scale rows below. A light brown spot,
smaller than iris, usually present on base of fourth to ninth rays of caudal fin. Posterior portions of dorsal fin and
upper 2/3 of caudal fin with faint oblique brown bars. Inner surface of pelvic fin with a large dusky patch.
Distribution. Specimens examined were collected from Japan and Taiwan. Three specimens were collected at
a depth of 183–188 m.
Remarks. Pietschmann (1911) provided 24 dorsal-fin rays for the holotype which we can confirm is correct;
however this appears atypical for the species, as the remainder of our material has 23, or rarely 22 rays. In the
original description the pectoral-fin ray count is given as 21; however the holotype has 21 on the right hand side
and 20 on the left hand side. We recorded only one other specimen with a count of 21 and 20, respectively, but
numerous individuals where the pectoral-fin ray counts differed by one ray between one side and the other. In
addition, the lateral-line scale count in the holotype was found to be 53, plus 2 small scales on caudal fin base,
instead of 62 as provided in the original description. These diagnostic characters are revised accordingly.
Parapercis macrophthalma is morphologically similar to P. mu ronis (Fig. 1D), having five transverse bars on
the upper body and sharing similar proportional measurements (Table 1), meristic counts (Table 2), squamation,
and arrangement of teeth on jaws, vomer and palatines. These two species co-occur in Taiwan and Japan.
Parapercis macrophthalma can be distinguished from P. muronis by having transverse bars on the body vertical
(vs. oblique) and all bars extending well below the lateral line (vs. 3rd to 5th bars ending on or above the lateral
line) and a slightly higher pectoral-fin ray count (19–21, modally 20 vs. 18–20, modally 19).
Examination of all known specimens identified as P. muronis in Taiwanese collections has revealed all but one
were misidentifications of P. macrophthalma. Shen (1984a) identified photographs of three individuals as P.
muronis (pl. 115, fig. 371-12a–c), of which two specimens (fig. 371-12a and fig. 371-12c, vouchers in NTUM, but
not sighted) are identical to P. macrophthalma, and one specimen (fig. 371-12b, NTUM 5613, 1 of 4, 97.4 mm SL)
is identical to P. muronis. Moreover, based on the figures and descriptions provided, Parapercis muronis of Masuda
et al. (1984: pl. 260, fig. E), Parapercis sp. of Shinohara (1997: 533, fig. 7), and Parapercis sp. 2 of Shimada
(2002: 1064) are here reidentified as P. macrophthalma.
Zootaxa 3620 (2) © 2013 Magnolia Press · 279
A NEW PARAPERCIS AND REDESCRIPTION OF P. MACROPHTHALMA
Department of Fisheries Malaysia (2009) recorded P. macrophthalma from Malaysia; however, we are unable
to verify the record due to the lack of any figure or voucher specimen.
Parapercis moki n. sp.
New English name: Mok’s sandperch
Figs. 2A–B, Table 1
Holotype. NMMB-P0892 (104.4 mm), Chong-Chou, Kaohsiung, southwestern Taiwan, northern South China Sea,
29 Nov. 1984, coll. M. Mok et al. (originally catalogued NSYU 1943).
Diagnosis. A species of Parapercis with relatively slender body; six transverse bars on upper body; numerous
small pores with canals forming about 9–10 vertical rows on cheek, opercle and subopercle; scales on nape
extending anteriorly to level of posterior margin of eyes; large spine on posteroventral corner of subopercle;
interorbital space very narrow (1.6% SL); and combination of the following characters: 4 dorsal-fin spines, each
spine progressively longer posteriorly, with last spine entirely connected by membrane to first dorsal-fin ray; 23
dorsal-fin soft rays; anal-fin with 1 spine and 19 soft rays; pectoral-fin rays 18 or 19; four pairs of canine teeth
anteriorly in lower jaw; palatine teeth present, in two rows; vomerine teeth stout, in two rows; scales on sides, belly
and prepectoral region ctenoid, becoming cycloid on nape and prepelvic areas; margin of preopercle smooth with
some small indentations on posterior margin; appressed pelvic fin not reaching origin of anal fin.
Description. Morphometric data based on the holotype are provided in Table 1. Dorsal-fin rays IV, 23; anal-fin
rays I, 19; all dorsal and anal soft rays branched, the last to base; pectoral-fin rays 18 (left side) and 19 (right side),
branched except uppermost; pelvic-fin rays I, 5; principal caudal-fin rays 9 (upper) + 8 (lower) =17; upper
procurrent caudal-fin rays 9; lower procurrent caudal-fin rays 7; pored lateral-line scales 56 (not including 2 pored
scales on base of caudal fin); scales above first lateral-line scale to origin of dorsal fin 4; scales above highest part
of lateral line to base of dorsal fin 3; scales below lateral line posteroventrally to origin of anal fin about 17; median
predorsal scales 12 (counted to level of posterior margin of eye); circumpeduncular scales 26; gill rakers of outer
first gill arch 5 + 9 = 14; pseudobranchial filaments 16; branchiostegal rays 6; vertebrae 10 + 23 = 33.
Body relatively slender, its depth 5.6 times in SL, 1.6 in HL; body subcylindrical anteriorly, the width 5.3 in
SL, 1.5 in HL, strongly compressed posteriorly; head relatively short, its length 3.5 in SL; ventral part of head,
chest, and abdomen slightly convex; snout relatively short, its length 3.3 in HL; eye relatively large, orbit diameter
3.1 in HL; interorbital space very narrow and flat, the least fleshy width 17.5 in HL; caudal-peduncle depth 3.5 in
HL; caudal-peduncle length 3.7 in HL.
Mouth large, the maxilla not quite reaching a vertical through center of eye, upper jaw relatively short, its
length 2.5 in HL; mouth slightly oblique, forming an angle of about 20° to horizontal axis of body, lower jaw
projecting; front of lower jaw with 4 pairs of recurved canine teeth, the middle one on each side twice as large as
the rest; side of upper jaw with row of about 24 slender conical teeth that curve medially and posteriorly, anterior 8
increasingly larger and more strongly recurved; remaining teeth in outer row on side of jaw decreasing in length;
broad band of villiform teeth medial to canines in about 7 rows at front of upper jaw, gradually narrowing
posteriorly to a narrow band in about 3 irregular rows; front of lower jaw with 4 pairs of incurved canine teeth,
increasing in length laterally, 4th twice as large as 1st and strongly curving laterally as well as posteriorly; band of
about 5 rows of villiform teeth medial to canines at front of lower jaw, medial row continuing laterally in jaw
posterior to last canine as row of 7 increasingly larger and more strongly recurved teeth, followed by a single row
of small teeth, with an additional inner row of 3 teeth at posterior part, to end of jaw; vomer with a triangular patch
of stout conical teeth, 7 on anterior margin largest, lateral and posterior ones progressively smaller; palatine with
two rows of stout teeth, those on outer row larger than those on inner row; lips smooth, their inner surface with
large fleshy papillae that interdigitate with anterior teeth; tongue broadly rounded, reaching forward to posterior
vomerine teeth.
Gill membranes free from isthmus, with a broad transverse free fold. Gill rakers short and spinous, longest
about half length of longest gill filament. Nostrils small, anterior nostril in front of center of eye (viewed from
side), a little less than half way to groove at margin of upper lip, with high anterior rim and pointed posterior flap
that reaches nearly anterior margin of posterior nostril when laid back; posterior nostril dorsoposterior to anterior
nostril, its aperture ovate, with slight anterior rim.
HO & JOHNSON
280 · Zootaxa 3620 (2) © 2013 Magnolia Press
Pores of cephalic sensory system as shown in Fig. 2. Row of 3 large pores above maxilla; 3 pores near nostrils,
one above, one between and one below; row of 3 pores on either side anteriorly in interorbital space; irregular
series of small pores medially on posterior half of interorbital space; numerous small pores with subcutaneous
canals posteriorly on occiput, pores divided into several irregular double series, from anterior end of lateral line on
body, continuing to ventral margin of eye, opercle and subopercle; cheek with 8–9 irregular double series; series of
10 small pores along the margin of preopercle; a series of 4 large pores on mandible; two medial pore at front of
chin.
Opercle with single sharp spine level with ventral edge of pupil (when viewed from side); subopercle with a
single sharp spine at posteroventral corner; preopercle broadly rounded, its free edge smooth except for slight
indentations at each pore site, extending from level of ventral edge of orbit downward and forward to slightly in
front of a vertical at posterior edge of orbit.
FIGURE 2. Parapercis moki n. sp., holotype, preserved condition, NMMB-P0892, 104.4 mm SL, Kaohsiung, southwestern
Taiwan. A. lateral view of the fish. B. dorso-lateral view of head pore pattern and squamation (upper) and pores on lower jaw
(lower).
Zootaxa 3620 (2) © 2013 Magnolia Press · 281
A NEW PARAPERCIS AND REDESCRIPTION OF P. MACROPHTHALMA
Scales finely ctenoid on body, becoming cycloid anterior to a line from base of third dorsal spine to anterior
end of lateral line, extending forward to a vertical from posterior margin of eye; scales on base of pectoral fin
ctenoid, those on area anterior to pelvic–fin base, opercle and subopercle cycloid; cheek scales cycloid, in about 9
irregular horizontal rows, relatively large and nonimbricate, extending anteriorly to a vertical from anterior 1/3 of
eye; progressively smaller scales extending out on basal portion of caudal fin for at least 2/3 length of fin; base of
pectoral fin with up to 4 rows of small cycloid scales; lateral line broadly arched over pectoral fin, then gradually
slanting to straight midlateral portion on about posterior fourth of lateral body.
Origin of dorsal fin over third lateral-line scale, predorsal length 3.3 in SL, equal to head length; 4 dorsal-fin
spines, all relatively slender, progressively longer posteriorly; 1st dorsal-fin spine 5.4 in HL; 2nd dorsal-fin spine
4.2 in HL; 3rd dorsal-fin spine 3.8 in HL; 4th dorsal-fin spine longest 3.3 in HL, full length of spine likely attached
to 1st soft ray by membrane (membrane damaged in holotype); last dorsal soft ray longest, 2.0 in HL; origin of anal
fin below base of 4th dorsal soft ray, preanal length 2.1 in SL; anal-fin spine 7.1 in HL; last anal soft ray longest,
2.4 in HL; caudal fin rounded, without prolonged upper lobe; total fin length 5.6 in SL, 1.6 in HL; pectoral fins
broadly rounded when spread, tenth ray longest, 4.6 in SL, 1.3 in HL; origin of pelvic fins anterior to pectoral-fin
origin, below base of exposed part of opercular spine, prepelvic length 3.7 in SL, 1.0 in HL; pelvic-fin spine
slender, 4.1 in HL; pelvic fins extending to genital papilla, but not reaching origin of anal fin; fourth soft pelvic ray
longest, 4.6 in SL, 1.3 in HL.
Color when fresh. Currently unknown.
Color in alcohol (Fig. 2A). Uniformly light brown with six slightly oblique narrow bars laterally on upper
body, each bar of about the same width, extending from base of dorsal fin to slightly below midbody; first bar at
front of spinous dorsal fin and posterior base of pectoral fin; second at base of 2nd–3rd dorsal-fin rays; third at
6th–7th rays; fourth at 11th–12th rays; fifth at 16th–17th rays; and sixth at 21st–22nd rays. A prominent black spot
at upper corner of caudal fin base, from the last procurrent to 7th ray of upper lobe, slightly larger than pupil of eye,
appearing non-ocellate. About 5 narrow oblique bars on caudal fin.
Distribution. Known only from the holotype collected from off Chong-Chou, Kaohsiung, southwestern
Taiwan.
Etymology. Named after Professor Hin-Kiu Mok, National Sun Ye-San University, in recognition of his
numerous contributions to fish studies and for providing the holotype for this study.
Comparison. Parapercis moki is unique within the genus in having many vertical rows of lateral-line pores on
the cheek. It is most similar to Parapercis sexlorata Johnson, 2006, these two being the only Parapercis species
with 6 narrow oblique black bars on the upper body. Parapercis moki can readily be distinguished from P. s ex lor at a
in having 4 pairs of conical teeth anteriorly in the outer row of the lower jaw (vs. three pairs) and a strong spine on
posteroventral corner of subopercle (vs. some feeble spinules). Parapercis moki is also similar to P. muronis and P.
macrophthalma in general appearance. It can be distinguished from both of the latter in having 4 dorsal-fin spines
(vs. 5); 6 narrow oblique black bars on upper body (vs. 5 vertical bars in P. macrophthalma and 5 oblique bars in P.
muronis); a prominent spot slightly larger than the pupil of the eye on the anterodorsal corner of caudal fin base (vs.
an relatively inconspicuous spot smaller than the pupil of the eye). Other Parapercis species with 4 dorsal fin
spines are easily distinguished by colouration.
A key to species of Parapercis with narrow transverse bars on the upper body
1A. Dorsal fin with 4 spines (rarely 5). . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2
1B. Dorsal fin with 5 spines (rarely 4). . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4
2A. Ten transverse bars on upper body . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . P. decemfasciata (Franz, 1910)
2B. Six transverse bars on upper body. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3
3A. Three pairs of conical teeth in outer row at lower jaw; feeble spinules on posteroventral corner of subopercle . . . . . . . . . . . . . .
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . P. sexlorata Johnson, 2006
3B. Four pairs of conical teeth in outer row at lower jaw; a large spine on posteroventral corner of subopercle. . . . . . . . . . . . . . . . .
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . P. moki Ho & Johnson, n. sp.
4A. No teeth on palatine. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .P. allporti (Günther, 1876)
4B. Teeth present on palatine. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5
5A. Five transverse bars on lateral body . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6
5B. Ten to 13 transverse bars on lateral body . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7
HO & JOHNSON
282 · Zootaxa 3620 (2) © 2013 Magnolia Press
6A. Transverse bars on body oblique, third to fifth ones usually ending above lateral line; modally 19 pectoral fin rays. . . . . . . . . .
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .P. muronis (Tanaka, 1918)
6B. Transverse bars on body vertical, third to fifth ones usually extending well below lateral line; modally 20 pectoral fin rays . . .
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . P. macrophthalma (Pietschmann, 1911)
7A. Pored lateral-line scales 58–60; 10 transverse bars on body, each extending to below midbody. . . . . . . . . . . . . . . . . . . . . . . . . .
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . P. multifasciata Döderlein, 1884
7B. Pored lateral-line 65–70; 13 short transverse bars on body, none extending below midbody . . . . . . .P. binivirgata White, 1904
Comparative materials. Parapercis muronis: BSKU 29197 (1 specimen, 91.2 mm SL); BSKU 29982 (1,
86.5); BSKU 36380 (1, 123.8) ; BSKU 36381 (1, 121.1); BSKU 36390 (1, 126.7); BSKU 36391 (1, 114.7); BSKU
36392 (1, 100.7); BSKU 37293 (1, 123.2); BSKU 42160 (1, 74.2); BSKU 42549 (1, 109.6); BSKU 42550 (1,
107.6); BSKU 43579 (1, 106.3); BSKU 44178 (1, 80.6); NSMT-P61134 (1, 74.2); NSMT-P 79900 (1, 54.0); all
collected from Japan. NTUM 5613 (1 of 4, 97.4), collected from Taiwan. Parapercis decemfasciata: ASIZP 58547
(1, 101); ASIZP 59484 (1, 104); ASIZP 59484 (1, 111.7); NMMB-P0487 (1, 96.8); NMMB-P0489 (2, 80.2–86.8);
NMMB-P11436 (1, 129.1); NMMB-P10044 (1, 124); all collected from Taiwan. Parapercis multifasciata: ASIZP
64301 (1, 96.8); ASIZP 60097 (1, 113); ASIZP 58609 (1, 134); NMMB-P10141 (2, 109.5–121.4); all collected
from Taiwan.
Acknowledgements
We are grateful to P. Bartsch (ZMB) and H. Endo (BSKU) for the loan of specimens under their care. We thank H.
Endo and N. Nakayama (BSKU) provide photos for this study; P.-L. Lin (ASIZP) for curatorial assistance. This
study is supported by the National Science Council (NSC 200-2621-B-291-001) and National Museum of Marine
Biology & Aquarium (NMMBA100200354).
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A rare species of sandperch, Parapercis okamurai, is redescribed based on 2 types and 15 specimens newly collected from Taiwan and Japan. The species is unique in having cycloid scales on the parietal, opercle and subopercle, except for few large ctenoid scale that covers the base of the opercular spine; body color yellowish dorsally, with 10 or 11 faint yellow bands on lateral body and pale ventrally; and black spots on inner side of upper pectoral fin base. It can also be distinguished from congeners by having a combination of the following characters: dorsal-fin rays V, 23; anal-fin rays I, 19; pectoral-fin rays 18; pored lateral-line scales 59-64; medial predorsal scales 9-10; transverse scale rows 4.5-5.5/14-15; circumpeduncular scales 20-21; gill raker4-5+9-10=13-16; -4 pairs of canine teeth at front of lower jaw; 2-4 rows of teeth on vomer; 2 rows of teeth on palatines; scales on cheek moderately large, each half embedded; and body color yellowish dorsally and a prominent ocellus at upper caudal-fin base.
... In recent decades, many new "cryptic" species sharing similar morphology or coloration in different speciescomplexes of the sandperch genus Parapercis Bleeker, 1863 have been described from throughout the Indo-west Pacific region (Randall & Francis, 1993;Randall, 2008;Johnson, 2006;Imamura & Yoshino, 2007;Randall et al., 2008;Liao et al., 2011;Ho & Shao, 2010;Ho & Johnson, 2013;Ho et al., 2012;Sparks & Baldwin, 2012;Allen & Erdmann, 2012;Johnson & White, 2012). The current number of valid species in Parapercis is 77; of these, 31 species were described in the last 10 years (Eschmeyer & Fong, 2013;Ho, pers. ...
Article
Parapercis albiventer sp. nov., a new species of sandperch is described based on 12 specimens collected from the western Indian Ocean. It can be distinguished from congeners by having a bright white ventral surface, without color markings on lower fourth of body; dorsal surface of head and body densely covered by small brown spots; a row of 10 faint reddish blotches on a paler background, along body axis; row of 10 deep reddish blotches, the lower part of each blotch with a solid black bar ventrally, below mid-lateral body axis; and combination of following characters: no palatine teeth; snout long; eye small; interorbital space broad; dorsal-fin rays V, 21; anal-fin rays I, 17; pectoral-fin rays 16-17; pored lateral-line scales 55-59; predorsal scales 9 or 10; scales on transverse row 6/17-21; 3 pairs of canine teeth at front of lower jaw; and vertebrae 10 + 20 = 30.
Article
Three new species of pinguipedid fishes from northern Australia are described based on specimens collected by deep water demersal trawling. Parapercis algrahami sp. nov. is recorded from off Dunk Island, Qld, south to Newcastle, NSW, in 67–333 m. It is distinct in having five narrow transverse dark bars across the upper body and a dark spot dorsally on the caudal-fin base, 6 canine teeth in outer row at front of lower jaw, palatines with 1–2 rows of teeth, and predorsal scales extending far forward on the nape to the posterior portion of the interorbital region. Parapercis imamurai sp. nov. is recorded from off Saumarez Reef, Qld, south to off Coffs Harbour, NSW, in 256–405 m. It is unique in having colouration that includes a broad dusky bar from lower margin of eye across the suborbital region and three broad dusky bands crossing the body between the middle of the soft dorsal-fin and the caudal-fin base, 10 canine teeth in outer row at front of lower jaw, and the fifth dorsal-fin spine longest. Parapercis pogonoskii sp. nov. is unique in having a combination of three reddish-brown vertical bars on the upper body between the anterior and posterior portions of the soft dorsal fin, the soft dorsal fin with two large dusky blotches and caudal-fin base with a dusky blotch in the upper corner, 8–10 canine teeth in outer row at front of lower jaw, fifth dorsal-fin spine longest, angle of subopercle with a single broad spine, and angle of preopercle with 4–5 large widely-separated spines. Comparison of the mitochondrial cytochrome c oxidase subunit 1 (CO 1) genetic marker utilised in DNA barcoding produced significant genetic divergences of at least 8.1% and 14.1% between P. algrahami sp. nov. and P. pogonoskii sp. nov. respectively and their closest sampled congeners. The geographic range of Parapercis rubromaculata Ho, Chang & Shao, 2012 is extended from Taiwan to the southern hemisphere waters off Western Australia, based on specimens collected from Shark Bay, north to Ashmore Terrace, in depths of 56–107 m. A revised diagnosis for the species is presented, meristic, morphometric and DNA barcoding data for the two populations are compared, and a detailed description of the colouration of fresh and preserved specimens from Australia is provided. Previous records of Parapercis macrophthalma (Pietschmann, 1911) from Western Australia are established as misidentifications of Parapercis muronis (Tanaka, 1918) and the latter is thereby confirmed from the southern hemisphere and Australian waters for the first time. Comparative meristic, morphometric and DNA barcoding data is provided for populations of P. muronis from Japan, Philippines and Western Australia.
Article
A single specimen of Parapercis randalli (Perciformes: Pinguipedidae) from Uchinoura Bay (31°17′N, 131°07′E), Kagoshima Prefecture, Japan at a depth of 40 m represented the second Japanese record and the northernmost record for the species, since the species has previously been recorded only from Taiwan (type locality) and Yoron-jima and Amami-oshima islands in the middle of the Ryukyu Islands, Japan. The specimen also represented the smallest example of 49.8 mm standard length (SL) in the species and differs from the larger previously known specimens (63.9–106.6 mm SL) in several characters, including slightly longer pelvic fin (26.8% SL vs. 18.0–22.2% SL) and caudal-fin lengths (24.3% SL vs. 20.2–22.1% SL); a red blotch on the upper caudal-fin base with an inner dark spot (vs. lacking inner spot); a single dark spot above the opercle (vs. two spots); and no spots on the soft-rayed portion of the dorsal fin (vs. a row of red or orangish brown spots present). These differences were regarded here as size-related variations within the species.
Article
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Johnson, J.W. 2006. Two new species of Parapercis (Perciformes: Pinguipedidae) from northeastern Australia, and rediscovery of Parapercis colemani Randall & Francis, 1993. Memoirs of Museum Victoria 63(1): 47–56. Two new species of pinguipedid fi shes, Parapercis fl avolabiata and P. sexlorata, are described. The former is known from 20 specimens collected by epibenthic sled and demersal trawl from within the Great Barrier Reef, Australia, between Anzac Reefs and Lady Musgrave Island, in depths from 45 to 79 m. It is most similar to Parapercis multiplicata Randall, 1984 and P. colemani Randall & Francis, 1993 in appearance, but is unique among the genus in having a combination of dorsal rays V, 21, anal rays I, 17–18, lateral-line scales 51–55, palatines edentate, angle of subopercle produced and with small spinules, 9–10 abdominal and 20 caudal vertebrae, and colouration including six broad red saddles across the back, a purplish-red line from the anterior edge of each orbit around the snout, and a series of yellow-edged red spots on the postorbital part of the head and nape. Parapercis sexlorata is described from seven specimens trawled off central eastern Australia between Cape Moreton, Queensland and North Solitary Island, New South Wales in 86 to 137 m. It is easily distinguished from its closest congeners with palatine teeth and dark transverse bars, P. macrophthalma Pietschmann, 1911 and P. muronis Tanaka, 1918, by having four rather than fi ve dorsal-fi n spines and six rather than fi ve transverse bars. Parapercis colemani Randall & Francis, 1993 was previously known only from the holotype, collected in 1.5 m depth in the lagoon of Norfolk Island. Additional specimens collected on the NORFANZ survey in the Tasman Sea indicate that the species usually inhabits much deeper habitats and occurs over a wider geographic area. New localities and meristic data are reported for the additional material.
Article
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The fishes of the genus Parapercis are popu- larly known as sandperch in the United States, grubfish in Australia, and sandsmelt in South Africa. The genus is much the largest of the Pin- guipedidae, the family name that replaced Parap- ercidae and Mugiloididae (Rosa and Rosa, 1987). Parapercis was described by Bleeker (1863: 236), who selected Sciaena cylindrica Bloch, 1792 as the type species. Cantwell (1964) was the first revisor of the genus, recognizing 27 species. Randall (1984) reviewed the genus, rais- ing the number of species to 40. The number of newly discovered species of Parapercis is show- ing no sign of decline. With the description of 6 new species from the western Pacific (Randall, in press), the total number of valid species will be raised to 67, of which 2 are from the Atlantic, 1 from the eastern Pacific, and the rest from the Indo-Pacific region. Abstract The following 3 new species of Parapercis from Japan are described, all with a smooth preopercular margin, small cycloid scales on the cheek, and no palatine teeth: P. basimaculata from the Ryukyu Islands in 40-70 m, distinct in having 54 lateral-line scales, stout conical teeth on vomer, caudal fin with a narrow prolonged upper lobe, 5 triangular red bars across body with a nar- row red bar between, and prominent dark brown spots basally in median fins; P. katoi from the Ogasawara Islands in 100-200 m, distinct in having 56-58 lateral-line scales, stout conical teeth on vomer, caudal fin with a prolonged upper lobe, and body with 5 broad red bars and a row of 10 small dark brown spots at level of origin of lateral line, 1 spot in first bar, 2 in each of remaining bars, and 1 at upper base of caudal fin; and P. natator in 15-45 m from Sagami Bay to the Ryukyu and Ogasawara Islands, distinct in having 59-61 lateral-line scales, 10-14 small conical teeth on vomer; very broad interorbital space (3.35-4.4 in head length), emarginate caudal fin in females, lunate in males, and unique in occurring in small aggregations above the bottom.
Book
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Results from a 5-year bottom trawl survey during the period 1979-1983 with photos/illustrations and descriptions, catch data and references. The full-text version is compressed. If anyone wants a printable version (358MB) feel free to contact me on tgtarp@me.com.
Article
An annotated checklist of fish genera and species described from Taiwanese waters through 2009 is presented. It includes 20 genera and 336 species/subspecies in 99 families. Of these, 225 species/subspecies are currently recognized as valid and 111 are invalid, including 7 questionable species. The current status of each taxon, if different from that of the original description, is provided. Thus far, 41 primary freshwater and estuarine species/subspecies are considered as endemic and 55 marine species are found only around Taiwan. The type series collected from Taiwan are also listed based on the information provided in the original descriptions and from our investigation. It includes approximately 2217 specimens in 779 lots, including 242 holotypes and lectotypes, 5 neotypes, 35 lots of syntypes and 497 lots of paratypes and paralectotypes. There are still 19 species lacking primary types and 11 lots with at least 31 unknown secondary type specimens.
Article
This study describes the genus Parapercis Bleeker and its 26 species. The descriptions are based on anatomical studies, each structure having been analyzed statistically to determine its variation within a species and its value in identification. An effort has been made to employ those characters with the least variation within species to establish possible affinities between species, to define species groups, and to determine relationships among them. The geographic range has been determined from actual specimens and the literature.
A synopsis of the vertebrates of Taiwan, second edition
  • References Chen
References Chen, J. T. F. (1969) A synopsis of the vertebrates of Taiwan, second edition. Commercial Press, Taipei, 173 pp. (in Chinese)
Ueber Neopercis macrophthalma n. sp. und Heterognathodon doederleini, Ishikawa, zwei Fische aus Formosa
  • V Pietschmann
Pietschmann, V. (1911) Ueber Neopercis macrophthalma n. sp. und Heterognathodon doederleini, Ishikawa, zwei Fische aus Formosa. Annalen des Naturhistorischen Museums in Wien, 25, 431–435.