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A redescription of grey pomfret Pampus cinereus (Bloch, 1795) with the designation of a neotype (Teleostei: Stromateidae)

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Pampus cinereus (Bloch, 1795) (Stromateidae), a species believed to be widely distributed throughout the Indo-Western Pacific region, was redescribed and a neotype was designated. The designation of a neotype was necessary because of ambiguous data in Bloch’s original description and the loss of the original type specimen. Morphological data indicated that 10 recently-collected specimens from the coasts of southern China agreed well with Bloch’s original description and figure of P. cinereus. A neotype for this species was selected from among the 10 specimens, and a detailed description is presented in this paper.
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Chinese Journal of Oceanology and Limnology
Vol. 31 No. 1, P. 140-145, 2013
http://dx.doi.org/ 10.1007/s00343-013-2039-9
A redescription of grey pomfret Pampus cinereus (Bloch,
1795) with the designation of a neotype (Teleostei:
Stromateidae)*
LIU Jing (刘静)
** , LI Chunsheng (李春生), NING Ping (宁平)
Laboratory of Marine Organism Taxonomy and Phylogeny, Institute of Oceanology, Chinese Academy of Sciences, Qingdao
266071, China
Received Mar. 20, 2012; accepted in principle May 3, 2012; accepted for publication Aug. 3, 2012
© Chinese Society for Oceanology and Limnology, Science Press, and Springer-Verlag Berlin Heidelberg 2013
Abstract Pampus cinereus (Bloch, 1795) (Stromateidae), a species believed to be widely distributed
throughout the Indo-Western Paci c region, was redescribed and a neotype was designated. The designation
of a neotype was necessary because of ambiguous data in Bloch’s original description and the loss of the
original type specimen. Morphological data indicated that 10 recently-collected specimens from the coasts
of southern China agreed well with Bloch’s original description and gure of P . cinereus . A neotype for this
species was selected from among the 10 specimens, and a detailed description is presented in this paper.
Keyword : Pampus cinereus ; neotype; China seas
1 INTRODUCTION
The genus Pampus (Stromateidae) was proposed
by Bonaparte (1837) and currently comprises six
species worldwide (Liu and Li, 1998a, b; Wu et al.,
1999; Nakabo, 2002; Liu, 2008; Froese and Pauly,
2012), Pampus argenteus (Euphrasen, 1788),
P . chinensis (Euphrasen, 1788), P . cinereus (Bloch,
1795), P . punctatissimus (Temminck et Schlegel,
1844), P . echinogaster (Basilewsky, 1855), and
P . minor (Liu et Li, 1998). The grey pomfret,
P . cinereus Bloch (1795), is a common species
distributed mainly in the Indo-Western Paci c. This
species was originally described by Bloch in 1795 in
the genus Stromateus , which is characterized by a
greatly extended anal n and notably long pectoral
ns. Subsequent workers, however, have long treated
the species as a member of Pampus (Day, 1959; Deng
et al., 1981; Wu, 1985; Liu and Li, 1998a, b; Wu et al.,
1999; Nakabo, 2000, 2002; Liu et al., 2002a, b; Liu,
2008; Shao, 2009; Cui et al., 2010; Froese and Pauly,
2011). However, Haedrich (1967) recognized only
three species of Pampus as valid: P . argenteus ,
P . echinogaster , and P . chinensis . Similarly, Last
(2001) treated only these three species in his recent
review of Stromateidae for the Food and Agriculture
Organization of the United Nations. Some previous
authors considered P . cinereus to be a synonym of
P . argenteus (Lindberg and Krasyukova, 1975; Parin
and Piotrovsky, 2004).
During our revisional studies of the genus Pampus ,
we encountered problems in identifying P . cinereus
and locating its type specimens. Fortunately, between
May 2010 and April 2011, we found 10 examples that
morphologically agreed well with the original
description and gure of P . cinereus by Bloch (1795).
Accordingly, P . cinereus (Bloch, 1795) is herein
redescribed based on 10 specimens from the coasts of
southern China, and a neotype is designated.
2 MATERIAL AND METHOD
Methods for measurements generally followed
Haedrich (1967) with some modi cations, and counts
of vertebrae and dorsal and anal rays were made from
radiographs. Total vertebrae were counted as the
number of precaudal vertebrae plus the number of
* Supported by the National Natural Science Foundation of China (Nos.
31172053, 41276166)
** Corresponding author: jliu@qdio.ac.cn
141No.1 LIU et al.: Redescription of Pampus cinereus
caudal vertebrae, including the urostylar vertebra
(=1). Lengths of specimens were given as standard
length; maximum body depth was given as body
depth, measured vertically at the origin of the rst
anal ray; head length was taken from the upper lip to
the posterior margin of the operculum; eye diameter
was the greatest distance between the free orbital
rims; interorbital width was the smallest distance
between the eyes; snout length was measured from
the anterior-most point of the upper lip to the nearest
eshy margin of the orbit; length of the upper jaw was
the distance from the symphysis of the premaxillaries
to the posterior end of the maxilla; length of the dorsal
n base was the distance from the base of rst dorsal
ray to the base of the last one; length of the anal n
base was the distance from the base of rst anal ray to
the base of the last one; predorsal distance was
measured from the tip of the snout to the base of the
rst dorsal ray; preanal distance was measured from
the anterior-most point of the lower jaw to the base of
the rst anal ray; caudal peduncle length was the
horizontal distance from the base of the last anal ray
to the origin of the caudal n base; caudal peduncle
depth was the least depth of the peduncle; lengths of
dorsal, anal, caudal, and pectoral ns were the lengths
of the longest rays. The morphometric data are
presented as percentages of standard length (SL) or
head length (HL). Measurements were made using a
vernier caliper and read to the nearest 0.1 mm. Gill
rakers were counted on the rst gill arch on both the
upper and lower limbs. Color and pigmentation were
noted in digital images of fresh specimens, but
detailed observations were made on specimens stored
in 70% ethanol after 10% formalin preservation.
Neotype: IOCAS41607, 145.0 mm SL, April 16,
2011, Zhuhai Fish Market, Guangdong Province,
China.
Other specimens: IOCAS6015, IOCAS6016,
IOCAS6070, three specimens, 141.5–147.5 mm SL,
May 9, 2010, Zhuhai Fish Market, Guangdong
Province, China; IOCAS30016, IOCAS30017, two
specimens, 115.5–142.0 mm SL, October 30, 2010,
Zhuhai Fish Market, Guangdong Province, China;
IOCAS14001, IOCAS14002, IOCAS14003, three
specimens, 143.5–158.5 mm SL, April 14, 2011,
Humen Fish Market, Guangdong Province, China;.
IOCAS41609, 142.0 mm SL, April 16, 2011, Zhuhai
Fish Market, Guangdong Province, China.
Comparative materials: IOCAS96-04,
IOCAS96-05, IOCAS96-13, IOCAS96-1001,
IOCAS98-19, IOCAS2123, IOCAS1076,
IOCAS1077, IOCAS1005, IOCAS1006, 10
specimens, 130.0–191.0 mm SL.
All specimens examined in this study are deposited
in the Museum of Marine Biology, Institute of
Oceanology, Chinese Academy of Sciences (IOCAS).
3 RESULT AND DISCUSSION
Pampus cinereus (Bloch, 1795)
(English name : grey pomfret, Fig.1)
Stromateus cinereus Bloch, 1795: 90, pl. 420 (no
locality); Bloch & Schneider, 1801: 491 (Tranquebar,
India); Günther, 1860: 346 (Malayan Peninsula).
Stromateus griseus Cuvier & Valenciennes, 1833:
391 (Pondichéry, Tamil Nadu, India).
Stromateoides cinereus Bleeker, 1864: 56 (Amoy,
China); Regan, 1902: 205 (China).
Pampus cinereus Fowler, 1934: 150 (Bangkok,
Thailand); Wu, 1985: 433, g. 665 (Fujian, China; in
part); Li, 1995: 195, g. 266 (East China Sea, in part);
Liu et al., 2002a: 243 (East China Sea, South China
Sea, in part).
Stromateus nozawae Cheng, 1962: 760, g.615
(South China Sea; in part); Yang and Cheng, 1987:
425, g.2216 (East China Sea and South China Sea;
in part).
3.1 Diagnosis
Pampus cinereus is distinguished from its
congeners in having the following combination of
characters: dorsal n rays 37–41; anal n rays 36–41;
anterior rays of dorsal and anal ns produced distinct
falcate lobes, preceded by 5–10 small blade-like
spines embedded in skin and not obvious in larger
specimens; anterior lobe of anal n greatly extended,
reaching behind the peduncle; rst anal n ray
originated below 5
th –6 th dorsal n ray; pectoral ns
extremely long (mean 44.8% of SL); caudal n deeply
forked, the lower lobe usually longer than the upper
one; gill rakers vestigial with 7–10 minute tubercular-
like spinules; total vertebrae 36, including 15
precaudal and 21 caudal vertebrae.
3.2 Description
Counts and proportional measurements of 10
specimens (including the neotype and nine non-type
specimens) of P . cinereus are given in Table 1.
D. viii–x, 37–41; A. v–vii, 36–41; P. 20–22; C.
22–24. Gr. 1–2+6–8=7–10; vertebrae 15+21=36.
As percentages of standard length: Maximum body
depth 61.3%–68.1%, head length 24.2%–27.7%,
142 CHIN. J. OCEANOL. LIMNOL., 31(1), 2013 Vol.31
dorsal- n length 33.5%–43.8%, anal- n length
48.4%–59.9%, pectoral- n length 42.0%–47.2%,
caudal- n length 43.3%–49.8%, predorsal distance
51.3%–59.7%, preanal distance 46.2%–55.8%, length
of dorsal- n base 49.8%–53.6%, length of anal- n
base 48.4%–55.9%, caudal peduncle length 9.4%–
10.1%, caudal peduncle depth 10.6%–11.7%.
As percentages of head length: Snout length
20.6%–23.2%, interorbital distance 42.1%–47.0%,
eye diameter 27.7%–30.7%, length of upper jaw
27.6%–29.3%.
Body deep, compressed and rhombic, covered by
small deciduous scales, of silvery grey color. Head
compressed; dorsal pro le strongly keeled, being
more prominent behind the eye; snout slightly
pointed. Eye small, greater than snout length. Mouth
small, subterminal; mouth slit curved downward
posteriorly, reaching to middle of eye; upper jaw
covered with skin, not moveable. Teeth on the jaws
minute, in a single row, narrowed from the sides;
teeth absent on the vomer and palatinum. Teeth absent
on entopterygoideum and metapterygoideum. Papillae
present in both halves of pharyngeal sacs.
Branchiostegal membrane fused with isthmus. Gill
membranes joined to belly; gill slit longer, its lower
margin below the level of pectoral- n base; total gill
rakers on rst gill arch vestigial with 7–10 min
tubercular-like spinules. Dorsal n rays 37–41; anal
n rays 36–41; both lobe-like anteriorly, originating
behind pectoral- n bases, preceded by 8–10 and 5–7,
respectively, short, blade-like spines with pointed
ends and embedded in skin in adults; anterior lobe of
anal n greatly extended, reaching behind the
peduncle. Caudal n long, deeply forked, lower lobe
usually extended. Pectoral ns notably long, with
20–22 rays. Pelvic ns absent.
Scales very small, cycloid, and deciduous,
extending onto bases of all ns. Head and nape with
well-developed network of longitudinal sensory
canals, posterior ends extending posterior to the
pectoral- n base. Lateral line high, following dorsal
pro le to caudal peduncle. Total vertebrae 36 (Fig.4).
3.3 Color of specimens
Color of fresh specimens: Dorsal and lateral
surfaces of head and body silvery grey, slightly bluish
grey on back, fading to pale grey on ventral sides.
Pectoral, anal, and caudal ns yellowish grey with
dark margins posteriorly; dorsal n dark grey.
Color of preserved specimens: Dorsal and lateral
surfaces of head and body brownish tan, fading to
pale brownish grey on ventral sides. The upper part of
pectoral ns and caudal n yellowish brown; dorsal
n brownish tan; anal n pale grey; all ns with dusky
margin posteriorly (Fig.1a).
Table 1 Comparative counts and proportional measure-
ments of neotype and non-type specimens of
Pampus cinereus and P . punctatissimus
P . cinereus P . punctatissimus
( n =10)
Neotype Non-type ( n =9)
Counts
Dorsal n ray ix, 39 viii–x–x, 37–41 vi–ix, 38–42
Anal n ray v, 37 v–vii, 36–41 v–vii, 34–42
Pectoral n ray 22 20–22 22–24
Caudal n rays 22 22–24 22–24
Gill rakers
(upper+lower=total) 1+7=8 1–2+6–8=7–10 2–3+8–10=10–13
Precaudal vertebrae 15 15 15
Caudal vertebrae 21 21 19
Total vertebrae 36 36 34
Measurements
Standard
length (mm) 145.0 117.5–158.5 130.0–191.0
As percentages
of SL
Maximum
body depth 62.1 61.3–68.1 58.5–68.5
Dorsal- n length 35.9 33.5–43.8 31.9–38.4
Anal- n length 50.3 48.4–59.9 40.3–50.8
Pectoral- n length 46.9 42.0–47.2 30.6–38.1
Caudal- n length 44.8 43.3–49.8 38.7–47.3
Predorsal distance 57.8 51.3–59.7 52.2–59.9
Preanal distance 50.7 46.2–55.8 53.0–56.9
Length of dorsal-
n base 53.3 49.8–53.6 48.1–57.4
Length of anal-
n base 53.0 48.4–55.9 46.3–54.5
Caudal-peduncle
length 10.0 9.4–10.1 10.0–11.7
Caudal peduncle
depth 11.7 10.6–11.6 9.2–11.5
Head length 25.5 24.2–27.7 22.5–28.3
As percentages
of HL
Snout length 22.2 20.6–23.2 23.0–29.4
Interorbital distance 42.4 42.1–47.0 41.2–48.1
Eye diameter 29.7 27.7–30.7 20.8–25.0
Length of upper jaw 28.6 27.6–29.3 25.4–30.2
143No.1 LIU et al.: Redescription of Pampus cinereus
3.4 Distribution
Pampus cinereus is known from China (Deng et
al., 1981; Wu, 1985; Wu et al., 1999; Liu et al., 2002a,
2002b; Liu, 2008), Japan (Nakabo, 2002), the
Malayan Peninsula (Günther, 1860), Thailand
(Fowler, 1934; Nakabo, 2002), and India (Bloch and
Schneider, 1801) and may range throughout the Indo-
Western Paci c.
3.5 Remarks
Pampus cinereus was rst described by Bloch
(1795) as Stromateus cinereus (Fig.1b) based on a
single stuffed specimen. The original description in
Bloch (1795) is brief and does not mention some
diagnostic characters used in this redescription to
discriminate Pampus species. The only data of
possible diagnostic value were the counts of dorsal
and anal n rays and the distinctly long pectoral ns.
However, the dorsal- and anal- n ray counts given in
the text of original description (D.35; A.29) did not
match those shown in the gure of the holotype (D.40;
A.41). Apparently, the values given in the text (D.35;
A.29) were a clerical error made by Bloch (1795),
because those characters are never observed in
Pampus . The values shown in the gure of the
holotype (D.40; A.41) could refer to at least two
species ( P . cinereus and P . punctatissimus ), which
both have greatly extended anal ns. However,
P . punctatissimus (Fig.2) lacks the long pectoral ns
of P . cinereus (over 40% SL).
Moreover, the type locality was not clear. Bloch
(1795) did not mention where the type specimen was
collected. For a long time, authors considered a single
specimen (ZMB 8754), which was originally
registered as a stuffed specimen deposited in the
Berlin Zoological Museum (ZMB), to be Bloch’s
holotype of Stromateus cinereus . Unfortunately,
Paepkes (1999) stated that type specimen ZMB 8754
was lost on page 145 in the book Blochs Fish
Collection in the Museum fuer Naturkunde der
Humboldt-University zu Berlin . Its loss was con rmed
by Dr. Peter Bartsch, the curator of sh division in the
Museum fuer Naturkunde (personal communication).
In the absence of a type specimen, the lack of critical
information in the original description, and the
uncertainties regarding the type locality, the identity
of this species can only be clari ed by a neotype
designation (International Code of Zoological
Nomenclature, art. 75. 3. 4).
To compare with P . cinereus
, only P . punctatissimus
from the Chinese coasts of the Yellow and East China
seas were used, because they have extended anal ns
and clearly conform with the species described by Liu
et al. (2002a). In overall body appearance, P . cinereus
is most similar to P . punctatissimus . However, it can
be clearly distinguished from the latter in having a
subterminal (vs. terminal) mouth, a shorter snout
(20.6%–23.2% vs. 23.0%–29.4% HL), a bigger eye
diameter (27.7%–30.7% vs. 20.8%–25.0% HL),
longer pectoral ns (42.0%–47.2% vs. 30.6%–38.1%
SL), and different numbers of total vertebrae (36 vs.
34). Furthermore, the gill rakers in P . cinereus
(Fig.3a) are vestigial with 7–10 minute tubercular-
like spinules (shorter than 1 mm) on the rst gill arch,
a
b
Fig.1 Pampus cinereus , neotype, IOCAS41607, 145.0 mm
SL (a); original gure (b) from Bloch (1795)
Fig.2 Pampus punctatissimus (Temminck et Schlegel, 1844),
IOCAS1005, 162.5 mm SL
144 CHIN. J. OCEANOL. LIMNOL., 31(1), 2013 Vol.31
but they are longer (more than 2 mm) with 10–13 in
the latter (Fig.3b).
4 ACKNOWLEDGEMENT
The authors are very grateful to Dr. Peter Bartsch,
Curator of Fishes, Museum fuer Naturkunde, and Dr.
Michael Tuerkay, Senckenberg Forschungsinstitut,
for providing important literature and information.
We also thank Prof. J. Y. LIU (Ruiyu LIU), Institute
of Oceanology, Chinese Academy of Sciences, for his
critical reading of the manuscript and Ms. Ying-Chun
SONG for translating Bloch’s article into Chinese.
References
Bleeker P. 1864. Notice sur les poissons envoyés de Chine. Au
Musée de Leide par M. G. Schlegel. Ned . Tyds . Dierk ., 2 :
55-62.
Bloch M E. 1795. Naturgeschichte der ausländischen Fische
Vol. 9. Schlesinger, Berlin. 192p.
Bloch M E, Schneider J G. 1801. Systema ichthyologiae
iconibus ex illustratum. Post obitum auctoris opus
inchoatum absolvit, correxit, interpolavit Jo. Gottlob
Schneider, Berolin. 584p.
Bonaparte C L. 1837. Iconogra a della fauna italica, per le
quattro classi degli animali vertebrati. Tome III, part 2,
Pesces, Roma. p.90.
Cheng Q T. 1962. Stromateidae. In : Zhang C L, Cheng Q T,
Zhu Y D, Zheng B S eds. Fishes of South China Sea.
p.760-763. (in Chinese)
Cui Z X, Liu Y, Li C P, Chu K H. 2010. Species delineation in
Pampus (Perciformes) and the phylogenetic status of the
Stromateoidei based on mitogenomics. Mol . Biol . Rep .,
38 : 1 103-1 114.
Cuvier G, Valenciennes M. 1833. Histoire naturelle des
poisons vol. 9. Nabu Press, Paris. 552p.
Day F. 1958. The Fishes of India: being a natural history of the
shes known to inhabit the seas and fresh waters of India,
Burma, and Ceylon. William Dawson, London. 778p.
Deng S M, Xiong G Q, Zhan H X. 1981. A comparative study
of the lateral line canal system of Chinese Stromateidae.
Acta Zool . Sinica , 27 (93): 232-239. (in Chinese with
English abstract)
Fowler H W. 1934. Zoological results of the third De
Schauensee Siamese Expedition, Part I: Fishes. Proc .
Acad . Nat . Sci . Philadephia ., 86 : 67-163.
Froese R, Pauly D. 2011. FishBase. World Wide Web electronic
publication. Available from: www. shbase.org. Accessed
on 2011-6-20.
Günther A. 1860. Catalogue of the Acanthopterygian Fishes in
the Collection of the British Museum Vol. 2. Taylor &
Francis, London. 548p.
Haedrich R L. 1967. The Stromateoid shes: systematics and a
classi cation. Bull . Mus . Comp . Zool ., 135 (2): 31-139.
Last P R. 2001. Stromateidae. In : Carpenter K E, Niem V H
eds. The Living Marine Resources of the Western Central
Paci c. Vol. 6. FAO, Rome. 4 218p.
Li C S. 1995. Stromateidae. In : Yamada U, Shirai S, Irie T,
Tokimura M, Deng S, Zheng Y, Li C, Kim Y U, Kim Y S
eds. Names and Illustrations of Fishes from the East
China Sea and the Yellow Sea. Overseas Fishery
Cooperation Foundation, Akasaka. 195p.
Lindberg G U, Krasyukova Z V. 1975. Fishes of the Sea of
Japan and the adjacent areas of the Sea of Okhotsk and
Yellow Sea part 4. Akad. Nauk SSSR, Leningrad. 332p.
Liu J. 2008. Vertebrata. In : Liu J Y ed. Checklist of Marine
Biota of China Seas. Science Press, Beijing. p.1 063. (in
Chinese)
Liu J, Li C S. 1998a. Redescription of a stromateoid sh,
Pampus punctatissimus (Temminck and Schlegel 1844)
and comparison with Pampus argenteus (Euphrasen
1788). Chin . J . Oceanol . Limnol ., 16 (2): 161-166.
Liu J, Li C S. 1998b. A new pomfret species, Pampus minor sp.
nov. Chin . J . Oceanol . Limnol ., 16 (3): 280-285.
Liu J, Li C S, Li X S. 2002a. Studies on Chinese pomfret
shes of the genus Pampus (Pisces: Stromateidae). Stud .
Mar . Sinica , 44 : 240-252. (in Chinese with English
abstract)
ab
4 mm
Fig.3 The comparison the rst left gill raker of Pampus
cinereus (a) and Pampus punctatissimus (b)
Fig.4 The radiograph of Pampus cinereus Bloch (1795),
neotype, IOCAS41607, 145.0 mm SL
The exposure condition is 40 kilovolt with 50 milliamperes-second. The
left white curve is the cord tied to the label of voucher number
145No.1 LIU et al.: Redescription of Pampus cinereus
Liu J, Li C S, Li X S. 2002b. Studies on the phylogeny and
biogeography of Chinese Pampus (Pisces: Stromateidae).
Stud . Mar . Sinica , 44 : 235-238. (in Chinese with English
abstract)
Nakabo T. 2000. Fishes of Japan with Pictorial Keys to the
Species (2
nd edn). Tokai Univ. Press, Tokyo. p.1 338-
1 345. (in Japanese)
Nakabo T. 2002. Fishes of Japan with Pictorial Keys to the
Species. Tokai Univ. Press, Tokyo. p.961-962.
Paepke H J. 1999. Bloch’s sh collection in the Museum für
Naturkunde der Humboldt-Universität zu Berlin—An
illustrated catalog and historical account. A.R.G. Gantner
Verlag KG, Czech Republic. p.145
Parin N V, Piotrovsky A S. 2004. Stromateoid shes (suborder
Stromateoidei) of the Indian Ocean (species composition,
distribution, biology, and sheries). J . Ichthyol ., 44 (Suppl.
1): 33-62.
Peng S, Shi Z, Hou J, Wang W, Zhao F, Zhang H. 2007. Genetic
diversity of silver pomfret ( Pampus argenteus ) populations
from the China Sea based on mitochondrial DNA control
region sequences. Biochem . Systs . Ecol ., 37 : 626-632.
Regan C T. 1902. A review of shes of the family Stromateidae.
Ann . Mag . Nat . Hist . Ser . 7, 10 : 205.
Shao K T. 2009. Taiwan Fish Database. World Wide Web
electronic publication. Available from www. shdb.sinica.
edu.tw. Accessed on 2012-2-20.
Wu H L. 1985. Stromateidae. In : Chu Y T ed. The Fishes of
Fujian Province vol. 2. Fujian Science and Techn. Press,
Fuzhou. p.431-433. (in Chinese)
Wu H L, Shao K T, Lai C F. 1999. Latin-Chinese Dictionary of
Fishes Names. The Sueichan Press, Keeloon. p.661.
Yang W H, Cheng Q T. 1987. Stromateidae. In : Cheng Q T,
Zheng B S eds. Systematic Synopsis of Chinese Fishes
Vol. 1. p.425. (in Chinese)
... Haedrich (1967) recognized three species in the genus Pampus, i.e., Pampus argenteus (Euphrasen, 1788), Pampus echinogaster (Basilewsky, 1855), and P. chinensis, and assigned many species names as synonyms of the three species. With recent efforts, Pampus cinereus (Bloch, 1795), Pampus candidus (Cuvier, 1829), and Pampus punctatissimus (Temminck & Schlegel, 1845) are resurrected as valid species; Pampus liuorum Pampus minor Liu andLi, 1998, are published as new species (Liu and Li, 1998a;Liu and Li, 1998b;Liu et al., 2013a;Liu et al., 2013b;Liu and Li, 2013), demonstrating that the genus Pampus is actually a more diverse group. Our previous study, Wei et al. (2021), confirmed the validities of seven species in the genus Pampus, viz., P. argenteus, P. candidus, P. chinensis, P. cinereus, P. liuorum, P. minor, and P. punctatissimus. ...
... In our previous study, Wei et al. (2021) provided reliable barcodes of cytochrome oxidase unit I (COXI) and cytochrome b (Cytb) from 74 specimens of seven Pampus species (i.e., P. argenteus, P. candidus, P. chinensis, P. cinereus, P. liuorum, P. minor, and P. punctatissimus). The specimens have been properly identified morphologically based on taxonomic works of the genus (i.e., Liu and Li, 1998a;Liu et al., 2013b;Liu et al., 2013a;Liu et al., 2013b;Radhakrishnan et al., 2019). A comparison of these barcodes with the global sequence data could provide valuable insight into the species diversity and distribution of the genus Pampus. ...
... In our previous study, Wei et al. (2021) provided reliable barcodes of cytochrome oxidase unit I (COXI) and cytochrome b (Cytb) from 74 specimens of seven Pampus species (i.e., P. argenteus, P. candidus, P. chinensis, P. cinereus, P. liuorum, P. minor, and P. punctatissimus). The specimens have been properly identified morphologically based on taxonomic works of the genus (i.e., Liu and Li, 1998a;Liu et al., 2013b;Liu et al., 2013a;Liu et al., 2013b;Radhakrishnan et al., 2019). A comparison of these barcodes with the global sequence data could provide valuable insight into the species diversity and distribution of the genus Pampus. ...
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Due to the highly similar external morphology of the Pampus species, misidentifications frequently occur and hinder the understanding of the taxonomy and species distributions of the genus. In this study, we generated 271 mitochondrial sequences and obtained 1,226 sequences from the public databases to understand the species diversity and distributions of the genus Pampus. Most phylogenetic analyses and species delimitations congruently concluded seven valid species within the genus Pampus (i.e., P. argenteus, P. candidus, P. chinensis, P. cinereus, P. liuorum, P. minor, and P. punctatissimus). Sequences of P. argenteus are reported through the northern South China Sea to the Japan Archipelago, which covered the type locality of P. echinogaster. Sequences of P. echinogaster in the public databases are all identified as P. argenteus, suggesting that the species should be synonymized with P. argenteus. Furthermore, sequences of P. griseus were identical to our P. cinereus data and, therefore, should be treated as a synonym of the latter. Inference on divergence time and ancestral distribution implied that the genus Pampus originated in the central Indo-Pacific region around 8.35–11.33 million years ago (the late Miocene), associated with the rise of the Indonesian–Australian Archipelago biodiversity hotspot. The divergence between P. cinereus and P. liuorum dated back to 1.20–1.72 million years ago, which might be related to glacial isolation during the Mid-Pleistocene transition.
... Latest global reports indicate the presence of the following seven valid species in the genus including the cryptic species described herein: Pampus argenteus, Pampus minor, Pampus punctatissimus, Pampus chinensis, Pampus cinereus, Pampus candidus, and Pampus sp. In 2017, Jawad and Jig, based on detailed comparative osteology of the axial skeleton, identified eight valid species in this genus, such as Pampus liuorum (Liu and Li, 2013) and Pampus nozawae (Ishikawa, 1904), which were found to be invalid by previous and subsequent researchers who considered them as synonyms of P. cinereus (Liu et al., 2013a;Li et al., 2019c;Yin et al., 2019). The existence of a strong geographic genetic structure in P. argenteus from the Indo-Western Pacific area was indicated (Sun et al., 2013), and a COI-based analysis of Pampus specimens by Divya et al. (2017) revealed the presence of seven distinct but taxonomically indecisive clades with two putative species viz. ...
... Our results agree that the Pampus sp. collected from the Indian Ocean by Divya et al. (2017) was closely related to the P. cinereus redescribed by Liu et al. (2013a) from China. The clustering of the three sister species, P. griseus, P. candidus, and P. cinereus ...
... However, both these complexes, characterized by greatly extended anterior rays of the anal fin, were not approved by subsequent researchers. In the first complex, P. nozawae, described by Ishikawa (1904), was proved to be an invalid species that was synonymized with P. punctatissimus and P. cinereus (Yamada et al., 2007;Liu et al., 2013a). It is to be added that P. nozawae, reported by Huang et al. (2016), from Daya Bay, China indeed represents P. cinereus. ...
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Pomfrets (genus Pampus), a highly commercial fishery resource distributed in the Indo-Western Pacific that includes Lessepsian migrants, have witnessed a series of systematic reforms. In this study, based on comprehensive sampling spanning type localities and coevals in the Northern Indian Ocean, the cryptic and valid species Stromateus griseus is resurrected from the synonymy and re-described as Pampus griseus (New Combination) based on 35 specimens from the Bay of Bengal, corroborated by a molecular analysis, which indicated a confined distribution of the species. The Bayesian phylogeny of the genus was reconstructed, incorporating redressed barcodes (582 nucleotides) and concatenated mitochondrial gene sequence data (1,822 nucleotides) generated from the recorded species P. candidus, P. chinensis and the neophyte along with sequences from GenBank entrusting the latest literature. The phylograms differed in topology as for seven valid species, and the one predicated on the concatenated data erected a highly supported polytomous clade for the P. cinereus complex (P. griseus, P. cinereus, and P. candidus) which shares synapomorphies. Pampus argenteus and P. minor, together, formed a sister clade to the rest. Climate-driven vicariant events during glacial epochs and the Indo-Pacific Barrier effect can be the drivers behind the Indian and Pacific Ocean sister lineages in P. chinensis. A multivariate analysis isolated the cryptic species from its congeners. This article portrays the systematics revision of genus Pampus with an integrative taxonomic approach compiling distinctive molecular, morphological, and anatomical features, revised key for species identification, taxonomic archives of Indian stromateids, and winds up with specific remarks.
... Pomfrets, species of genus Pampus Bonaparte, 1834, family Stromateidae Rafinesque, 1810, are pelagic marine fishes widely distributed along the coast of the Indo-West Pacific region. Seven valid species of genus Pampus have been recognized, namely, Pampus argenteus (Euphrasen, 1788), P. candidus (Cuvier, 1829), Pampus chinensis (Euphrasen, 1788), Pampus cinereus (Bloch, 1795), Pampus minor , Pampus nozawae (Ishikawa, 1904, and Pampus punctatissimus (Temminck & Schlegel, 1845) [1][2][3][4][5][6][7][8][9]. They contribute high commercial values to fisheries of the countries along the coast of the Indo-West Pacific region. ...
... Liu et al. [3], based on the original description and type locality of P. argenteus, redescribed the species and designated its neotype, which set up a reference for verifying validities of its junior synonyms. Simultaneously, the neotype of P. cinereus was assigned and described by Liu et al. [6] as a substitution of its lost holotype. Liu and Li [2] described a novel species, Pampus liuorum Liu & Li, 2013, based on its distinct morphology compared with six known pomfret species. ...
... However, a morphological comparison indicated that P. echinogaster sensu Li et al. [12] is similar to the neotype of P. argenteus designated in Liu et al. [3], and thus could be a misidentification. Pampus nozawae used to be considered as a junior synonym of P. cinereus [6]. Its validity was recently proposed based on its distinct axial skeletal morphology comparing to its congeners [8], although a redescription and neotype designation of this species are currently unavailable. ...
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The genus Pampus contains seven valid species, which are commercially important fishery species in the Indo-Pacific area. Due to their highly similar external morphologies, Pampus liuorum has been proposed as a synonym of Pampus cinereus. In this study, partial sequences of COI (582 bp) and Cytb (1077 bp) were presented as potential DNA barcodes of six valid Pampus species and the controversial species P. liuorum. A species delimitation of the seven Pampus species was performed to verify their validities. Explicit COI barcoding gaps were found in all assessed species, except for P. liuorum and P. cinereus, which resulted from their smaller interspecific K2P distance (0.0034–0.0069). A Cytb barcoding gap (0.0200) of the two species was revealed, with a K2P distance ranging from 0.0237 to 0.0277. The longer Cytb fragment is thus a more suitable DNA barcode for the genus Pampus. In the genetic tree, using concatenated Cytb and COI sequences, the seven species reciprocally formed well-supported clades. Species delimitations with ABGD, GMYC, and bPTP models identified seven operational taxonomic units, which were congruent with the seven morphological species. Therefore, all of the seven analyzed species, including P. liuorum, should be kept as valid species.
... Pampus cinereus was originally briefly described by Bloch (1795) on the basis of only one dry specimen of unknown type locality, which was subsequently lost, denying further examination (Liu et al. 2013a). Ichthyologists previously believed that P. cinereus was synonymous with P. argenteus and P. punctatissimus (Wang 1958;Fowler 1972;Zhu et al. 1985;Parin and Piotrovsky 2004). ...
... Ichthyologists previously believed that P. cinereus was synonymous with P. argenteus and P. punctatissimus (Wang 1958;Fowler 1972;Zhu et al. 1985;Parin and Piotrovsky 2004). To address the inconsistencies surrounding the classification of P. cinereus, Liu et al. (2013a) examined specimens of P. cinereus, describing its morphological characteristics. However, the authors failed to describe the morphology of the transverse occipital canal of the lateral line, a key diagnostic characteristic. ...
... According to the sampling sites and other relevant studies (Zhu et al. 1985;Liu et al. 2002bLiu et al. , 2013a, we conclude that P. cinereus is primarily distributed throughout the waters south of the Taiwan Strait and those extending southward toward the Malaysian peninsula. ...
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Pomfret, which are widely distributed throughout the western Pacific and Indian Oceans, are economically important fish species. As their similar external morphological characteristics can inhibit proper species identification, numerous errors exist in the morphological characterization and DNA barcoding data of pomfret. In this study, we extensively sampled pomfret from the Indian and Pacific Oceans. Using the sampled specimens, in combination with morphological assessments, DNA barcoding, and corrected sequences of the mitochondrial cytochrome c oxidase I (COI) gene in GenBank, we attempted to resolve the classification issues surrounding this group. We identified seven valid species in the genus Pampus, of which all seven are distributed in the western Pacific and three are distributed in the Indian Ocean. Pampus argenteus, Pampus cinereus, and Pampus sp. were identified as three valid species with relatively close genetic distances and sharing a common ancestor. Significant variation between Pampus chinensis specimens from the Arabian Sea and the northwestern Pacific suggest a possible species complex. Finally, we provide an identification key to facilitate the identification of pomfret based on the major diagnostic morphological characteristics of six Pampus species collected along the western Pacific coast. On the basis of the reports on the new record of “Pampus argenteus,” we found that the Lessepsian migration of pomfret was likely, with species from the Indian and Pacific Oceans spreading through the Mediterranean Sea into the waters of the eastern Atlantic. Further study is required to clarify the validity of the newly recorded “Pampus argenteus.”
... The name Pampus, a masculine noun, is from the vernacular of the 19th century East Indian Spanish and Portuguese colonials, who generally used the term "pampus" (ultimately from "pompano") for any silvery, compressed fish. The genus Pampus was proposed by Bonaparte (1837) and currently includes eight species distributed worldwide (Liu and Li 2013;Eschmeyer et al. 2017) viz.: Pampus argenteus (Euphrasen 1788;Liu et al. 2013b), P. chinensis (Euphrasen 1788), P. cinereus (Bloch 1793(Bloch , 1795Liu et al. 2013a), P. punctatissimus (Temminck and Schlegel 1845), P. echinogaster (Basilewsky 1855), P. minor (Liu and Li 1998) and P. liuorum (Liu and Li 2013). The eighth species, P. nozawae (Ishikawa 1904), was considered a synonym of P. cinereus by Liu et al. (2013a), but Jawad and Jig (2016) have recently confirmed the validity of this species based on studies of the axial skeleton. ...
... The genus Pampus was proposed by Bonaparte (1837) and currently includes eight species distributed worldwide (Liu and Li 2013;Eschmeyer et al. 2017) viz.: Pampus argenteus (Euphrasen 1788;Liu et al. 2013b), P. chinensis (Euphrasen 1788), P. cinereus (Bloch 1793(Bloch , 1795Liu et al. 2013a), P. punctatissimus (Temminck and Schlegel 1845), P. echinogaster (Basilewsky 1855), P. minor (Liu and Li 1998) and P. liuorum (Liu and Li 2013). The eighth species, P. nozawae (Ishikawa 1904), was considered a synonym of P. cinereus by Liu et al. (2013a), but Jawad and Jig (2016) have recently confirmed the validity of this species based on studies of the axial skeleton. ...
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Pomfrets (Genus Pampus) are commercially important fish in the Indo-Pacific region. The systematics of this genus is complicated because of morphological similarities between species. The silver pomfret from Indian waters has long been considered to be Pampus argenteus. Morphological and molecular examination of specimens from the Arabian Sea and Bay of Bengal regions suggested the silver pomfret from the region represents two species that are distinct both from each other and from P. argenteus from the South China Sea. Based on detailed morphological, meristic and molecular examinations, the most common species from the Indian Ocean was found to correspond with the descriptions of Stromateus candidus (Cuvier), which is resurrected from the synonymy of P. argenteus and redescribed here as Pampus candidus (new combination). The second species, which has restricted distribution in Indian waters needs further studies to arrive at taxonomic conclusions and is hence not described in the current study. Lectotypes are also designated for Pampus candidus.
... The genus Pampus (Perciformes: Stromateidae) comprises five species [15], that is, P. chinensis, P. cinereus, P. minor, P. argenteus and P. punctatissimus, all of which are pelagic fishes and multiple batch spawners [16,17]. Only two species of this genus, P. chinensis and P. cinereus, are widespread across the Indian Ocean and the Northwest Pacific [18,19]. Samples of P. cinereus collected from the Bay of Bengal have been reported to have close affinity to the P. cinereus in the South China Sea but are genetically distinct [20,21]. ...
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Among marine species distributed in the Indian Ocean and the Pacific, the Indo–Pacific Barrier (IPB) has been found to be an important barrier of divergence of species distributed on both sides. Among the five species of the genus Pampus, only Pampus chinensis and P. cinereus are distributed across the western Pacific and the Indian Oceans and have not been studied comparatively using extensive sampling and gene markers. Furthermore, the origin and history of genus Pampus remain unrevealed. We used thousands of nuclear loci based on target gene enrichment to explore genetic structure of P. chinensis and P. cinereus across the western Pacific and Indian Oceans. We performed divergence dating and ancestral area reconstruction analysis and inferred the dispersal routes of the Pampus species. The results suggest that the IPB played an important role in the differentiation between populations among the two oceans for both P. chinensis and P. cinereus, dividing species into the Pacific lineage and the Indian Ocean lineage. Low sea level in the late Pleistocene may be the main cause. The result also showed that the South China Sea was the center of origin of the genus Pampus, and dispersal routes of each species may be associated with the ocean currents. Our study provided new examples for the IPB effect on marine species.
... A lack of catch records for S. taty has limited the use of conventional assessment methods, so that this species cannot be assessed quickly and accurately. Recorded catches of P. argenteus have often included several related species, thereby confounding previous evaluations of its stock status (see Liu et al., 2013). Our application of ensemble methods by combining length-based models provides a solution which facilitates accurate evaluation of the state of stocks in which mixing of species in catches or other deficiencies in reported catches may occur. ...
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For many fish stocks, such as Pampus argenteus and Setipinna taty in China, size composition data are more accessible than catch data. Varied results can arise when different length-based stock assessment models are applied to these data, and fishery managers often need to reconcile conflicting estimates of population status. Superensemble modeling, a relatively recent innovation in fish stock assessments commonly used in other fields, may provide an effective solution to resolving uncertainties among the results from multiple length-based models. To verify potential for this approach to improve estimates of population status, we applied ensemble modeling to fit simulated data of P. argenteus and S. taty in the Bohai and Yellow Seas using predictions from a length-based integrated mixed effects (LIME) and length-based spawning potential ratio (LB-SPR) models as covariables in a superensemble model developed in this study. All simulation modeling of P. argenteus and S. taty in the Bohai and Yellow Seas was conducted using the operating model in the R package LIME. Initially, the LIME and LB-SPR performances were tested separately under three scenarios of fishing mortality and recruitment variability (“equilibrium scenario,” “endogenous scenario,” and “one-way base scenario”). Then, estimates of spawning potential ratio (SPR) were combined with the superensemble models (a linear model, a support vector machines, a random forest and a boosted regression tree). We trained our superensemble models with 80% of the simulated data and tested them with the remaining 20%. Our results showed that superensemble modeling substantially improved the estimates of SPR, with support vector machines performing the best at estimating population status: precision improved by 12.7% for S. taty and 8% for P. argenteus on average (namely, median absolute proportional error decreased by 0.127 and 0.08 on average) compared to the individual models. This finding has important implications for fisheries management in the context of species for which catch data are unavailable. Applying the size composition survey data, the results from support vector machines superensemble model suggested that neither S. taty nor P. argenteus in the Bohai Sea in 2019 are overfished, but the stock status of P. argenteus warrants vigilant monitoring.
... Pampus argenteus originally described by Euphrasen (1788) based on a specimen from Guangdong province, China, was characterized as having a dorsal fin with 9 min spines and 45 rays, and an anal fin with 7 min spines and 43 rays. Some author think P. cinereus as a synonym of P. argenteus (Froese and Pauly, 2018;Haedrich, 1967;Li et al., 2017;Sun, 2015), whereas others accept P. cinereus as a valid species (Cui et al., 2011;Cui et al., 2010;Divya et al., 2017;Liu et al., 2013b). Pampus cinereus has fewer dorsal fin rays (37-41 vs 45) and anal fin rays (36-41 vs 43) compared to the original description of P. argenteus (Liu et al., 2013a) (Table 2). ...
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Pampus is a widespread species of fish in the western Pacific and Indian Oceans that has significant commercial worth. Its evolutionary history and phylogenetics are still poorly understood, and details on its intraspecific taxonomy are debatable, despite some morphological and molecular research. Here, we analyzed this species using skeletal structure data as well as nuclear (S7 gene) and mitochondrial genetic information (COI, D-loop and mitogenomes). We found that the genetic distance between P. argenteus and P. echinogaster was much smaller than that between other Pampus species, and both maximum likelihood and Bayesian phylogenetic trees yielded almost identical tree topologies. An additional and adjacent M repeat was found in the downstream region of the IQM gene cluster of P. argenteus and P. echinogaster, and the trnL2 gene of P. minor was translocated. The genus Pampus experienced early rapid radiation during the Palaeocene with major lineages diversifying within a relatively narrow timescale. Additionally, three different methods were conducted to distinguish the genus Pampus species, proving that P. argenteus and P. echinogaster are the same species, and P. liuorum is speculated to be a valid species. Overall, our study provides new insights not only into the evolutionary history of Pampus but its intraspecific taxonomy as well.
Article
The genetic diversity of silver pomfret (Pampus argenteus) from the Bohai, East China, and South China Seas was investigated using mitochondrial DNA (mtDNA) control region sequence data. We found high levels of variation with 17 haplotypes among the 45 individuals (h=0.88, π=0.006). AMOVA analysis detected significant structuring among China Sea silver pomfret (P0.05). Whether silver pomfret from the South China Sea exhibit a different demographic history than those from the Bohai and East China Seas remains to be determined.