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Oxynoemacheilus kiabii, new species, from Karkheh River drainage, Iran, is distinguished from other species of Oxynoemacheilus by having two lateral pores in each side of the supratemporal canal and no central pore, no suborbital flap or suborbital groove in males, a slightly emarginate caudal fin, an incomplete lateral line, a very long head, and distinct, large and vertically elongated blotches on flank, most prominent behind dorsal-fin base. © 2011 by Verlag Dr. Friedrich Pfeil, München, Germany - ISSN 0936-9902.
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ISSN 0936-9902
Ichthyological Exploration
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Number 3
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Ichthyological Exploration of Freshwaters
An international journal for field-orientated ichthyology
Volume 22 Number 3 September 2011
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Ichthyol. Explor. Freshwaters, Vol. 22, No. 3
Copyright © Verlag Dr. Friedrich Pfeil
Ichthyol. Explor. Freshwaters, Vol. 22, No. 3, pp. 201-208, 4 figs., 1 tab., September 2011
© 2011 by Verlag Dr. Friedrich Pfeil, München, Germany – ISSN 0936-9902
Oxynoemacheilus kiabii,
a new loach from Karkheh River drainage, Iran
(Teleostei: Nemacheilidae)
Kiavash Golzarianpour*, Asghar Abdoli** and Jörg Freyhof***
Oxynoemacheilus kiabii, new species, from Karkheh River drainage, Iran, is distinguished from other species of
Oxynoemacheilus by having two lateral pores in each side of the supratemporal canal and no central pore, no
suborbital flap or suborbital groove in males, a slightly emarginate caudal fin, an incomplete lateral line, a very
long head, and distinct, large and vertically elongated blotches on flank, most prominent behind dorsal-fin base.
* Department of Biology, Faculty of Sciences, Gonbad Kavous University, Gonbad, Iran; and
Department of Zoology, Faculty of Biological Sciences, Shahid Beheshti University, G. C., Tehran, Iran.
E-mail: kiavash.pro@gmail.comE-mail: kiavash.pro@gmail.com
** Department of Biodiversity and Ecosystem Management, Environmental Sciences Research Institute, Shahid
Beheshti University, G. C., Tehran, Iran. E-mail: asabdoli@yahoo.com
*** Leibniz-Institute of Freshwater Ecology and Inland Fisheries, Müggelseedamm 310, 12561 Berlin, Germany.
E-mail: freyhof@igb-berlin.de
Introduction
The main obstacles in the study of the nemachei-
lid loaches of the Middle East are the confused
definitions of the genera (see Freyhof et al., 2011)
and the high number of poorly diagnosed species
described from this area. For example, nemachei-
lid loaches occur in almost all water bodies in
Iran (Abdoli, 2000) but Nalbant & Bianco (1998),
who reviewed the nemacheilid loaches of that
country, mentioned only 14 species and sug-
gested that additional nine species do occur as
they are known from adjacent areas but have not
yet been found in Iran (Nalbant & Bianco, 1998).
Since, only Turcinemacheilus kosswigi was added
to the fauna of the country (Golzarianpour et al.,
2009) and Ilamnemacheilus longipinnis has been
described as a new species from Iran (Coad &
Nalbant, 2005). Not even very ubiquitous species
such as Oxynoemacheilus argyrogramma, which is
present at almost every locality in the Euphrates
and Tigris drainages in Turkey, have been re-
corded from Iran, simply because most nemachei-
lid species from the Middle East are poorly diag-
nosed and almost impossible to identify. During
several field campaigns in Turkey, Syria, Jordan
and Iran, we were able to collect fresh material
from the type localities of most Middle East
nemacheilid species and the types of 15 species
have been examined (Freyhof et al., 2011). These
background data allow us to compare unidenti-
fied nemacheilids with described species. While
it is still premature to publish a full taxonomic
review of nemacheilids of the Middle East, the
202 Copyright © Verlag Dr. Friedrich Pfeil
Golzarianpour et al.: Oxynoemacheilus kiabii
available background data already allow describ-
ing new species from certain species groups. It is
the aim of this study to describe a very distinct
new species of Oxynoemacheilus from Iran.
Material and methods
All fish except the holotype and FSJF 3224 were
preserved in 5 % formaldehyde and stored in
70 % ethanol. The holotype and FSJF 3224 were
preserved in 99 % ethanol. Measurements were
made with dial caliper and recorded to 0.1 mm.
All measurements are made point to point,
never by projections. Methods for counts and
measurements follow Kottelat & Freyhof (2007).
Standard length (SL) is measured from the tip of
the snout to the end of the hypural complex. The
length of the caudal peduncle is measured from
behind the base of the last anal-fin ray to the end
of the hypural complex, at mid-height of the
caudal-fin base. The depth of the caudal peduncle
is measured directly anterior to the ventral adi-
pose crest including the dorsal crest if present.
The last two branched rays articulating on a
single pterygiophore in the dorsal and anal fins
are noted as 1 1
/
2
. The holotype is included in
the calculation of means and SD.
Abbreviations used: SL, standard length; HL,
lateral head length; CMK, Collection of Maurice
Kottelat, Cornol; FSJF, Fischsammlung J. Freyhof,
Berlin; FCKG, Fish Collection K. Golzarianpour,
Tehran; HUIC, Department of Biology, Hacette-
pe University, Ankara; IZA, Universita degli
Studi dellAquila, Instituto di Zoologia, Aquila;
NMP, National Museum, Prague; NMW, Natur-
historisches Museum, Vienna; ZFMK, Zoologi-
sches Forschungsmuseum Alexander Koenig,
Bonn; ZISP, Zoological Institute of Russian Acad-
emy of Sciences, St. Petersburg; ZMH, Zoologi-
sches Museum Hamburg. See Freyhof et al. (2011)
for a detailed list of specimens examined.
No material of O. lenkoranensis and O. leontinae
was available to us. We use the data published
by Abdurakhmanov (1962) and Krupp (1985),
respectively.
Oxynoemacheilus kiabii, new species
(Figs. 1-3)
Holotype. ZFMK 41847, 54.5 mm SL; Iran: Ha-
madan prov.: stream Dehnoo, 3 km west of Na-
havand on road from Nahavand to Sarab-e-
Gamasiab, 34°10' N 48°24' E; K. Golzarianpour, 10
May 2007.
Paratype. All from Iran: Hamadan prov.: FCKG
8658, 8, 31.4-50.7 mm SL; FCKG 8659, 7, 33.1-
56.55 mm SL; FSJF 3003, 7, 33.6-53.3 mm SL; same
locality as holotype; K. Golzarianpour, 4 July 2010.
– FSJF 3004, 2, 38.4-44.4 mm SL; stream Babaros-
tam, a tributary to Gamasiab River; 34°10'18" N
48°21'23" E; A. Abdoli & K. Golzarianpour, 15 Mar
2008.
Additional material (non types). FSJF 3224, 16, 34-
49 mm SL; Iran: Hamadan prov.: Gamasiab River.
Diagnosis. Oxynoemacheilus kiabii is distinguished
from all other species of Oxynoemacheilus by hav-
ing two, rarely one or three lateral pores in the
Fig. 1. Oxynoemacheilus kiabii, ZFMK 41847, holotype, 54.5 mm SL; Iran: stream Dehnoo. Note that the black spots
on body and fins are not part of the colour pattern but the result of a severe diplostomiasis infection that affected
all collected specimens.
203
Ichthyol. Explor. Freshwaters, Vol. 22, No. 3
Copyright © Verlag Dr. Friedrich Pfeil
supratemporal canal and no central pore; no
suborbital flap or groove in males; caudal fin
slightly emarginate; lateral line incomplete, reach-
ing dorsal-fin base; head very long (length 26-
30 % SL); pectoral fin short, not reaching to pelvic-
fin origin; dorsal adipose crest shallow, reaching
from vertical of base of last anal-fin ray to ante-
rior part of caudal fin; distinct, large, vertically
elongated blotches on flank, most prominent
behind dorsal-fin base.
Description. See Figures 1-3 for general appear-
ance and Table 1 for morphometric data of holo-
type and 16 paratypes. Small, stout and deep
bodied species with long and wide head. Body
deepest at about midline between nape and
dorsal-fin origin, depth decreasing slightly to-
wards caudal-fin base. A conspicuous hump at
nape in many individuals. Greatest body width
behind head. Section of head trapezoid, flattened
on dorsal and ventral surface. Caudal peduncle
compressed laterally, 0.8-1.2 (mean 1.0) times
longer than deep. A short, triangular axillary lobe
at base of pelvic fin, completely attached to body.
Pelvic-fin origin below branched dorsal-fin rays
1-2. Pectoral fin reaching approximately 60-75 %
of distance from pectoral-fin origin to pelvic-fin
origin. Pelvic fin not reaching or reaching anus.
Anus situated about one eye diameter in front of
anal-fin origin. Anal fin not reaching caudal-fin
base. Dorsal adipose crest on caudal peduncle
reaching forward to vertical of base of last anal-fin
Fig. 2. Oxynoemacheilus kiabii, ZFMK 41847, holotype, 54.5 mm SL; Iran: stream Dehnoo. Note that the black spots
on body and fins are not part of the colour pattern but the result of a severe diplostomiasis infection that affected
all collected specimens.
Fig. 3. Oxynoemacheilus kiabii, FCKG 8658, paratype, 45.1 mm SL; Iran: stream Dehnoo. Note that the black spots
on body and fins are not part of the colour pattern but the result of a severe diplostomiasis infection that affected
all collected specimens.
204 Copyright © Verlag Dr. Friedrich Pfeil
ray. Shallow ventral adipose crest on caudal
peduncle reaching forward below middle of last
anal-fin ray when folded along caudal peduncle.
Margin of dorsal fin convex. Caudal fin slightly
emarginate. Median caudal-fin rays 82-96 %
(mean 88) of length of upper caudal-fin lobe.
Largest known specimen 56.5 mm SL.
Dorsal fin with 8
1
/
2 branched rays. Anal fin
with 5
1
/
2 branched rays. Caudal fin with 8 + 8
branched rays. Pectoral fin with 10 and pelvic fin
with 8 rays. Body covered by embedded scales,
except on back in front of dorsal fin and belly.
Lateral line incomplete, with 18-29 pores, reach-
ing under dorsal-fin base. Anterior nostril open-
ing on anterior side of a low, pointed and flap-like
tube. Nostrils separate, posterior tip of anterior
nostril not reaching to posterior nostril when
folded down. Two lateral pores in supratemporal
canal, no central pore. In two individuals one
lateral pore on left side and two on right side, in
one individual three pores on each side. No cen-
tral pore in supratemporal canal but in one indi-
vidual, both upper lateral pores almost on mid-
line. No suborbital flap or groove in males.
A shallow, wide groove on snout between eye
and base of outer rostral barbel in both sexes.
Mouth small, strongly arched. Lips thick, with
well marked furrows. A deep median interruption
in lower lip. A small median incision in upper
lip. Processus dentiformis small and pointed. No
median notch in lower jaw. Barbels very short,
inner rostral barbel not reaching base of maxillary
barbel; outer one reaching slightly beyond base
of maxillary barbel, not reaching vertical of ante-
rior margin of eye. Maxillary barbel reaching
vertical of middle of eye. Males with slightly
longer pectoral fin than females.
Coloration. Body pale brown in life and grey in
preserved individuals. Flank with 10-19 large,
Golzarianpour et al.: Oxynoemacheilus kiabii
Table 1. Morphometric data of Oxynoemacheilus kiabii (holotype ZFMK 41847, paratypes FCKG 8658, FCKG
8659; n = 16).
holotype range including holotype
mean min max SD
Standard length (mm) 54.5 41.3 31.4 52.2 6.3
In percent of standard length
Head length 22.7 25.2 23.3 28.4 1.4
Body depth at dorsal-fin origin 22.9 22.7 20.0 25.2 1.7
Prepectoral length 27.5 27.7 24.5 30.4 1.3
Predorsal length 52.1 53.9 48.2 57.2 2.1
Postdorsal length 34.9 35.5 31.8 38.0 1.8
Preanal length 79.6 78.0 75.0 84.6 2.0
Prepelvic length 58.0 58.2 53.7 63.1 2.3
Distance between pectoral and pelvic-fin origins 25.9 28.3 24.6 31.7 1.8
Distance between pelvic and anal-fin origins 16.6 17.1 14.0 19.5 1.4
Distance between vent and anal-fin origin 2.8 2.0 1.1 2.6 0.5
Depth of caudal peduncle 15.3 14.7 13.0 16.8 1.1
Length of caudal peduncle 13.0 17.6 15.8 20.0 1.1
Dorsal-fin depth 19.1 19.5 17.0 21.6 1.2
Anal-fin base length 7.7 8.1 6.5 9.2 0.8
Pectoral-fin length 18.2 19.4 17.1 21.4 1.2
Pelvic-fin length 11.8 13.7 12.1 14.4 0.6
In percent of head length
Head depth at eye 79.5 72.6 64.3 84.1 5.2
Snout length 45.7 45.6 32.2 52.0 4.8
Eye diameter 20.4 21.6 17.5 26.9 2.1
Postorbital distance 56.8 53.3 44.5 60.4 4.1
Maximum head width 85.5 82.9 71.3 94.8 6.4
Interorbital width 38.9 41.5 37.8 47.7 2.7
Length of inner rostral barbel 17.5 19.1 12.8 26.5 2.9
Length of outer rostral barbel 26.6 22.8 17.4 31.7 3.4
Length of maxillary barbel 23.7 26.7 17.6 38.5 5.3
205
Ichthyol. Explor. Freshwaters, Vol. 22, No. 3
Copyright © Verlag Dr. Friedrich Pfeil
irregular shaped, dark brown or black blotches.
Flank blotches in front of dorsal fin origin usu-
ally smaller and organised in very irregular
vertical rows of 2-3 blotches in some individuals,
dissociated into a mottled pattern in other indi-
viduals. Blotches usually narrower or equally
spaced compared to interspaces on anterior body
and wider than interspaces on posterior body.
Blotches more regular on body behind dorsal-fin
origin, vertically elongated and forming bars.
Lateral blotches usually dissociated from similar
sized blotches on predorsal back. Blotches never
forming saddles. Flank blotches smaller below
than above lateral line. An irregularly shaped,
prominent dark brown or black bar at posterior
extremity of caudal peduncle dissociated into two
half-moon shaped blotches in some individuals.
Head with many small spots and blotches some-
times fused into a marbled pattern. Dorsal and
caudal fins with a tessellated pattern on rays,
spots forming 2-3 narrow and irregular bars on
caudal fin and 3 wide bands on dorsal fin. Anal-,
pelvic- and pectoral fins with few dark brown or
black spots on rays.
Note that the black spots on body and fins in
specimens on Figures 1-3 are not part of the
colour pattern but the result of a severe infection
by diplostomiasis that affected all collected
specimens; as a result, it is not possible to illustrate
an intact individual. The infection masks the tes-
selated pattern on the fins.
Distribution and habitat. Oxynoemacheilus kiabii
was collected in the Karkheh River drainage. The
Karkheh is a tributary of the Karoun, which flows
into the lowermost part of the Tigris. It was col-
lected in clear water streams with swift current
(Fig. 4).
Etymology. The species is named for Bahram H.
Kiabi in appreciation for his contribution to the
conservation of the vertebrates of Iran, especially
fishes.
Remarks. Oxynoemacheilus kiabii is described in
the genus Oxynoemacheilus following the key of
Middle East loaches provided by Freyhof et al.
(2011). It is also superficially very similar to
O. frenatus, O. tongiorgii and O. panthera; unpub-
lished molecular data show that these species
belong to Oxynoemacheilus. Oxynoemacheilus kiabii
belongs to a group of species which lack a sub-
orbital flap or suborbital groove in males (vs.
present in O. anatolicus, O. angorae, O. araxensis,
O. banarescui, O. bergianus, O. brandtii, O. bureschi,
O. cinica, O. erdali, O. eregliensis, O. evreni, O. ger-
mencicus, O. hamwii, O. mediterraneus, O. paucilepis,
O. phoxinoides, O. pindus, O. samanticus, O. seyhani-
cola, O. simavicus, O. theophilii and O. tongiorgii).
In O. kosswigi and O. merga the outline of the
suborbital groove is still visible in some indi-
viduals but its lower edge is completely fused
with the surrounding skin and there is no slit. In
O. argyrogramma, a species usually without sub-
orbital flap or groove, there are individuals, in
which the flap is completely covered by skin and
invisible externally. In other individuals there is
a short slit in the skin at the lower margin of the
lachrymal bone while in other individuals there
is an open, long slit at the lower margin of the
bone and the posterior margin of the lachrymal
bone is elevated.
Oxynoemacheilus kiabii is similar to O. argyro-
gramma, O. ceyhanensis, O. insignis, O. kosswigi,
O. lenkoranensis, O. merga and O. namiri by the
absence of a suborbital flap or groove (sometimes
present in O. argyrogramma). It is distinguished
from these species by having a very slightly
emarginate caudal fin (vs. deeply emarginate or
forked). The caudal fin is also slightly emarginate
in O. cyri, O. ercisianus, O. frenatus, O. galilaeus,
O. kaynaki, O. kermanshahensis, O. leontinae, O. pan-
thera, O. seyhanensis and O. tigris and these species
also lack a suborbital flap or groove. It is unknown
whether males O. leontinae have a suborbital flap
and we were not able to examine material of this
species.
Oxynoemacheilus kiabii is distinguished from
O. frenatus, O. galilaeus, O. kermanshahensis, O. sey-
hanensis and O. tigris by the absence of the central
pore in the supratemporal canal (vs. central pore
present) and by having usually two lateral pores
in each side of the supratemporal canal (vs. one).
The middle supratemporal pore is present and
there are two lateral pores in each side of the
canal in O. kaynaki. In O. cyri, O. ercisianus and
O. panthera, the middle pore is absent in most but
not all individuals and there are 1-3 lateral pores
in each side of the canal, often set in an asym-
metric pattern. We have no information about the
pores in the supratemporal canal in O. leontinae
as we were not able to examine material of this
species. Species with a suborbital flap or groove
or with deeply emarginate or forked caudal fin
were not examined for this character.
Beside the absence of the median pore in the
206 Copyright © Verlag Dr. Friedrich Pfeil
supratemporal canal, O. kiabii is distinguished
from O. kaynaki and O. seyhanensis by an incom-
plete lateral line reaching under the base of the
dorsal-fin (vs. complete, reaching to posteriormost
part of caudal peduncle) and a color pattern of
very large, vertically elongated and distinct
blotches (vs. marbled). The lateral line is also
incomplete in O. cyri, O. ercisianus, O. frenatus,
O. galilaeus, O. leontinae, O. kermanshahensis,
O. panthera and O. tigris.
Oxynoemacheilus kiabii occurs in sympathy
with O. kermanshahensis in Karkheh drainage.
Besides having four (vs. three) pores in the su-
pratemporal canal, O. kiabii is further distin-
guished from O. kermanshahensis by a color pattern
of very large, vertically elongated and distinct
blotches (vs. a prominent, irregularly shaped
midlateral stripe from head to caudal-fin base),
a longer head (length 26-30 % SL vs. 16-23), and
a shorter snout (32-52 % HL vs. 42-58).
Oxynoemacheilus kiabii is sympatric and even
syntopic with O. frenatus, which is very wide-
Golzarianpour et al.: Oxynoemacheilus kiabii
spread in Euphrates and Tigris drainages. Oxy-
noemacheilus kiabii is distinguished from O. frena-
tus by the absence of a central pore usually in the
supratemporal canal (vs. presence), four to six
pores in the supratemporal canal (vs. usually three
pores, five in one individual), a color pattern of
very large, vertically elongated and distinct
blotches most distinct on flank behind dorsal-fin
base (vs. flanks irregularly spotted or marbled),
a longer head (length 26-30 % SL vs. 23-26) and
a smaller predorsal distance (48-52 % SL vs. 51-
56).
Oxynoemacheilus kiabii is distinguished from
O. galilaeus from Jordan drainage by the flank
covered by scales (vs. absent), 8
1
/
2 branched
dorsal-fin rays (vs. 9 1
/
2-11 1
/
2) and a color pattern
of very large, vertically elongated and distinct
blotches (vs. small dots).
Oxynoemacheilus kiabii is distinguished from
O. leontinae from Litani and Jordan drainages by
a color pattern of very large, vertically elongated
and distinct blotches (vs. irregularly marbled or
Fig. 4. Stream Dehnoo, type locality of Oxynoemacheilus kiabii.
207
Ichthyol. Explor. Freshwaters, Vol. 22, No. 3
Copyright © Verlag Dr. Friedrich Pfeil
with small dots) and by having a longer head (HL
26-30 % SL vs. 22-26).
Oxynoemacheilus kiabii is distinguished from
O. ercisianus from Lake Van basin by having a
deeper caudal peduncle (depth 0.8-1.2 times in
its length vs. 1.5-1.9) and a longer head (HL 26-
30 % SL vs. 23-26).
Oxynoemacheilus kiabii is distinguished from
O. panthera from endorheic streams near Damas-
cus by a longer head (HL 26-30 % SL vs. 25-26)
and a shorter dorsal adipose crest reaching for-
ward to the vertical of the base of the last anal-fin
ray (vs. long crest reaching forward to the poste-
rior tip of the dorsal fin when folded down or
even below the last dorsal fin-rays, elevated in
middle in some individuals), and a color pattern
of very large, vertically elongated and distinct
blotches (vs. irregularly marbled or with small
dots).
Oxynoemacheilus kiabii is distinguished from
O. tigis from Qweik and Euphrates drainages by
having a shorter dorsal adipose crest reaching
forward to the vertical of the base of the last anal-
fin ray (vs. long crest starting between the tip of
the last dorsal-fin ray to the anterior half of the
anal-fin base, elevated in middle in some indi-
viduals), a color pattern of very large, vertically
elongated and distinct blotches (vs. irregularly
set bars) and a longer head (HL 26-30 % SL vs.
22-26).
Oxynoemacheilus kiabii is distinguished from
O. cyri from Kura and Aras Rivers by a color pat-
tern of very large, vertically elongated and distinct
blotches usually not meeting on the back (vs.
regular or irregular set bars meeting on back) and
a longer head (HL 26-30 % SL vs. 24-26). In O. cyri,
there is a variable pattern of pores in the supratem-
poral canal, some individuals have three pores
including the central pore, others have four in a
symetric pattern without a central pore, others
have four pores in a asymmetric pattern and one
individual has six pores in an asymmetric pat-
tern.
Oxynoemacheilus kiabii is superficially similar
to the two species of Seminemacheilus by lacking
a suborbital flap in males, having a slightly emar-
ginate caudal fin and an incomplete lateral line.
It is distinguished from Seminemacheilus lendlii
and S. ispartaensis by the short pectoral fin in males
(reaching to 60-75 % of distance between pectoral-
fin and pelvic-fin origins vs. reaching beyond
vertical of dorsal-fin origin) and by a different
colour pattern (prominent large blotches without
sexual dimorphism vs. small spots and dots in
females, a dark lateral stripe in males in some
populations). It is further distinguished from
S. ispartaensis by having 8
1
/
2 dorsal-fin rays (vs.
7 1
/
2) and from S. lendlii by the lateral-line reaching
the vertical of the dorsal-fin origin (vs. not reach-
ing). Also, O. kiabii is a small species with very
short barbels while S. ispartaensis reaches 90 mm
SL and both Seminemacheilus have very long bar-
bels. Seminemacheilus tongiorgii was transferred to
Oxynoemacheilus by Freyhof et al. (2011). Oxy-
noemacheilus kiabii is immediately distinguished
from O. tongiorgii by the absence of a suborbital
flap in males (vs. presence).
Acknowledgment
We are pleased to thank Alexander Naseka (ZISP) for
examining O. lenkoranensis for us, Füsun Erkakan
(HUIC), Ralf Thiel (ZMH) and Helmut Wellendorf
(NMW) for allowing JF to examine materials in their
collections, Pier Giorgio Bianco (IZA) for the paratypes
of O. farsicus, Radek Sanda (NMP) for the loan of O. pin-
dus, Maurice Kottelat (CMK) for the loan of O. cyri and
helpful comments on the manuscript, Mahdi Ghalenoi
(Tehran) for help during fieldwork in Iran, Müfit
Özulug, Cem Dalyan and Özcan Gaygusuz (Istanbul)
for help during fieldwork in Turkey, Nisreen Alwan,
Kai Borkenhagen, and Florian Wicker (Frankfurt) for
help during fieldwork in Syria and Jordan, and Kayvan
Abbasi for providing material of O. bergianus from
Sefid River. We especially thank Babak Hafezi (Tehran),
for accompanying us on many terrible roads in the field
in Iran.
References
Abdurakhmanov, Y. A. 1962. [Freshwater fishes of
Azerbaidzhan]. Akademii Nauk Azerbaidzhanskoi
SSR, Institut Zoologii, Baku, 407 pp.
Erkakan, F., T. T. Nalbant & S. C. Özeren. 2007. Seven
new species of Barbatula, three new species of
Schistura and a new species of Seminemacheilus
(Ostariophsi: Balitoridae: Nemachilinae) from Tur-
key. Journal of Fisheries International, 2: 69-85.
Freyhof, J., F. Erkakan, C. Özeren & A. Perdices. 2011.
An overview of the western Palaearctic loach genus
Oxynoemacheilus (Teleostei: Nemacheilidae). Ich-
thyological Exploration of Freshwaters, in press.
Golzarianpour, K., A. Abdoli, B. Kiabi & J. Freyhof.
2009. First record of the miniature loach Turci-
noemacheilus kosswigi (Teleostei: Nemacheilidae) in
the Karoun drainage, Iran. Zoology of the Middle
East, 47: 57-62.
208 Copyright © Verlag Dr. Friedrich Pfeil
Golzarianpour et al.: Oxynoemacheilus kiabii
Kottelat, M. & J. Freyhof. 2007. Handbook of European
freshwater fishes. Kottelat, Cornol and Freyhof,
Berlin, xiv + 646 pp.
Krupp, F. 1985. Systematik und Zoogeographie der
Süsswasserfische des levantinischen Grabenbruch-
systems und der Ostküste des Mittelmeers. Disser-
tation, Johannes Gutenberg Universität, Mainz,
215 pp.
Nalbant, T. T. & P. G. Bianco. 1998. The loaches of Iran
and adjacent regions with description of six new
species (Cobitoidea). Italian Journal of Zoology, 65:
109-123.
Received 30 March 2011
Revised 12 September 2011
Accepted 8 October 2011
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INSTRUCTIONS TO CONTRIBUTORS
Ichthyological Exploration of Freshwaters
An international journal for field-orientated ichthyology
Articles appearing in this journal are indexed in:
AQUATIC SCIENCES and FISHERIES ABSTRACTS
BIOLIS - BIOLOGISCHE LITERATUR INFORMATION SENCKENBERG
CAMBRIDGE SCIENTIFIC ABSTRACTS
CURRENT CONTENTS/AGRICULTURE, BIOLOGY & ENVIRONMENTAL SCIENCES and SCIE
FISHLIT
ZOOLOGICAL RECORD
C O N T E N T S
Ou, Chouly, Carmen G. Montaña, Kirk O. Winemiller and Kevin W. Conway: Schistura
diminuta, a new miniature loach from the Mekong River drainage of Cambodia (Tele-
ostei: Nemacheilidae) ................................................................................................................. 193
Golzarianpour, Kiavash, Asghar Abdoli and Jörg Freyhof: Oxynoemacheilus kiabii, a new
loach from Karkheh River drainage, Iran (Teleostei: Nemacheilidae) ............................... 201
Kottelat, Maurice and Tan Heok Hui: Systomus xouthos, a new cyprinid fish from Borneo,
and revalidation of Puntius pulcher (Teleostei: Cyprinidae) ................................................ 209
Kottelat, Maurice and Tan Heok Hui: Rasbora atranus, a new species of fish from central
Borneo (Teleostei: Cyprinidae) ................................................................................................. 215
Costa, Wilson J. E. M.: Hypsolebias nudiorbitatus, a new seasonal killifish from the Caatinga
of northeastern Brazil, Itapicuru River basin (Cyprinodontiformes: Rivulidae) .............. 221
Fernández, Luis, Jael Dominino, Florencia Brancolini and Claudio Baigún: A new catfish
species of the genus Silvinichthys (Teleostei: Trichomycteridae) from Leoncito National
Park, Argentina ........................................................................................................................... 227
Costa, Wilson J. E. M.: Phylogenetic position and taxonomic status of Anablepsoides, Atlan-
tirivulus, Cynodonichthys, Laimosemion and Melanorivulus (Cyprinodontiformes: Rivul-
idae) .............................................................................................................................................. 233
Conway, Kevin W., Maurice Kottelat and Tan Heok Hui: Review of the Southeast Asian
miniature cyprinid genus Sundadanio (Ostariophysi: Cyprinidae) with descriptions of
seven new species from Indonesia and Malaysia .................................................................. 251
Ichthyological Exploration of Freshwaters
An international journal for field-orientated ichthyology
Volume 22 Number 3 September 2011
Cover Photograph
Sundadanio axelrodi (photograph by Koji Yamazaki)
Kevin W. Conway, Maurice Kottelat and Tan Heok Hui
(this volume pp. 251-288)
... Oxynoemacheilus karunensis [E]-[NE], Karun stone loach/Tigris (Persian Gulf basin)(Freyhof, 2016b;Sayyadzadeh & Esmaeili, 2020).167. Oxynoemacheilus kiabiiGolzarianpour, Abdoli & Freyhof, 2011 [E]-[NE], Kiabi stone loach/Tigris (Persian Gulf basin)(Golzarianpour et al., 2011).168. Oxynoemacheilus kurdistanicusKamangar, Prokofiev, Ghaderi & Nalbant, 2014 [N]-[NE], Kurdistan stone loach/Tigris (Persian Gulf basin)(Kamangar et al., 2014). ...
... Oxynoemacheilus karunensis [E]-[NE], Karun stone loach/Tigris (Persian Gulf basin)(Freyhof, 2016b;Sayyadzadeh & Esmaeili, 2020).167. Oxynoemacheilus kiabiiGolzarianpour, Abdoli & Freyhof, 2011 [E]-[NE], Kiabi stone loach/Tigris (Persian Gulf basin)(Golzarianpour et al., 2011).168. Oxynoemacheilus kurdistanicusKamangar, Prokofiev, Ghaderi & Nalbant, 2014 [N]-[NE], Kurdistan stone loach/Tigris (Persian Gulf basin)(Kamangar et al., 2014). ...
Article
The current status of the inland waters ichthyofauna of Iran is revised and updated. A total of 292 fish species belong to 3 classes, 24 orders, 36 families and 106 genera inhabit the inland waters of Iran. Among these, 29 species (9.9%) are exotic and 102 species (35%) are endemic. Orders with the largest numbers of species in the ichthyofauna of Iran are the Cypriniformes (182 species) followed by Gobiiformes (30 species), Cyprinodontiformes (15 species), Siluriformes (12 species), Clupeiformes (10 species), Acipenseriformes and Cichliformes (7 species) and Mugiliformes (6 species). At the family level, the Cyprinidae has the greatest number of species (74 species; 25.34% of the total species), followed by the Nemacheilidae (47 species), Leuciscidae (42 species), Gobiidae (30 species), Aphaniidae (11 species), Clupeidae (10 species), Acipenseridae and Cichlidae and Sisoridae (7 species in each) and Cobitidae and Mugilidae (6 species).
... Found in Aras River drainage. Taxonomy: Coad (1995) and Prokofiev (2009) placed O. angorae as subspecies but Golzarianpour et al. (2011) give it full rank species. ...
... Taxonomy: Golzarianpour et al. (2011) Diagnosis: Flank with a set of dark or brown blotches in mid-lateral elongated, back with 3-4 separated dark brown roundish to elongated blotches a deep and obivious suborbital groove in males, usually 3-4 lateral and 3 central opening in supratemporal canal, body and caudal peduncle are deep (17.3-19.4 and 10-11% SL, respectively) and caudal fin slightly emarginated. ...
Article
Full-text available
This is an annotated checklist of all recognized and named taxa of freshwater fishes of Iran, documenting recent changes and controversies in nomenclature, and including primary synonyms, updated from the Jouladeh-Roudbar et al. (2015b) checklist. We provide an updated comprehensive listing of taxonomy, diagnostic and meristic characters, names, and conservation status, including detailed distribution maps. We strive to record the most recent justified taxonomic assignment of taxa in a hierarchical framework, providing annotations, including alternative possible arrangements, for some proposed changes. We provide common English and Persian names and detailed distributional data for all taxa, listing occurrence by basins, including indications of native, endemic, and translocated populations. We used the IUCN Red List Categories and Criteria for classifying species at high risk of global extinction. The diversity of freshwater fishes of Iran included in this checklist, consists of 274 recognized species in 100 genera, 33 families, 20 orders and 3 classes. Also, for the first time we report and confirm the presence of seven species Aphanius kruppi, Capoeta kaput, Luciobarbus conocephalus, Oxynoemacheilus veyselorum, O. gyndes, O. hanae and Squalius latus from Iran basins. The confirmed freshwater fishes of Iran comprise 264 species in 97 genera, 33 families, 20 orders and 3 classes. Of the 241 endemic and native fish species listed the conservation statuses are as follows, 1 Extinct in the Wild (EW), 17 Critically Endangered (CR), 12 Endangered (EN), 15 Vulnerable (VU), 9 Near Threatened (NT), 148 Least Concern (LC) and 39 Data Deficient (DD). Forty four fish species (18.3% of 241 species listed) are officially regarded as globally Threatened (Critically Endangered [CR], Endangered [EN], or Vulnerable [VU]). These numbers and percentages of Threatened species have increased since the last checklist.
... Little is known about the nemacheilid loaches of Western Asia because of their small size and low value for marketing (Golzarianpour et al. 2009). About 30 species in six genera have been reported from Iran (Nalbant & Bianco, 1998;Coad & Nalbant, 2005;Prokofiev, 2009;Golzarianpour et al. 2011), but this is predicted to be incomplete. ...
... Etymology: This species is named from Zagros Mountains; adjective. (Krupp, 1992) (Heckel, 1843), O. seyhanensis (Bănărescu, 1968) and O. tigris (Heckel, 1843), but can be easily distinguished by the complete lateral line (vs incomplete in all the compared species: Krupp & Schneider, 1989;Freyhof et al. 2011;Golzarianpour et al. 2011). O. namiri (Krupp & Scheider, 1991) sometimes possesses an almost complete lateral line; however, it can be easily distinguished from O. zagrosensis by the stout spine-shaped posterior processes of the bony air-bladder capsule and in the color pattern consisting of regular vertical cross-bars (Krupp & Schneider, 1991). ...
Article
For the first time, we present data on species composition and distributions of nemacheilid loaches in the Choman River basin of Kurdistan province, Iran. Two genera and four species are recorded from the area, of which three species are new for science: Oxynoemacheilus kurdistanicus, O. zagrosensis, O. chomanicus spp. nov., and Turcinoemacheilus kosswigi Băn. et Nalb. Detailed and illustrated morphological descriptions and univariate and multivariate analysis of morphometric and meristic features are for each of these species. Forty morphometric and eleven meristic characters were used in multivariate analysis to select characters that could discriminate between the four loach species. Discriminant Function Analysis revealed that sixteen morphometric measures and five meristic characters have the most variability between the loach species. The dendrograms based on cluster analysis of Mahalanobis distances of morphometrics and a combination of both characters confirmed two distinct groups: Oxynoemacheilus spp. and T. kosswigi. Within Oxynoemacheilus, O. zagrosensis and O. chomanicus are more similar to one other rather to either is to O. kurdistanicus. Key words: Nemacheilidae, Iran, Kurdistan, taxonomy, new species.
... ‫قرار‬ ‫بررسی‬ ‫مورد‬ ‫نیز‬ ‫ها‬ ‫ایستگاه‬ ‫انتخاب‬ ‫مطالعه،‬ ‫این‬ ‫انجام‬ ‫براي‬ ‫مطالعة‬ ‫براساس‬ ‫ها‬ ‫تمام‬ ‫که‬ ‫گردید‬ ‫انتخاب‬ ‫نحوي‬ ‫دو‬ ‫محلول‬ ‫در‬ ‫بالفاصله‬ ‫شده‬ ‫صید‬ ‫ماهیان‬ ‫گردد.‬ ‫شامل‬ ‫را‬ ‫دسترس‬ ‫قابل‬ ‫هاي‬ ‫آب‬ ‫ماهیان‬ ‫میدانی‬ ‫راهنماي‬ ‫براساس‬ ‫بیهوشی‬ ‫از‬ ‫بعد‬ ‫و‬ ‫شدند‬ ‫داده‬ ‫قرار‬ ‫میخک‬ ‫گل‬ ‫درصد‬ ( ‫ایران‬ ‫داخلی‬ ‫هاي‬Golzarianpour et al., 2011;Freyhof, 2016;Esmaeili et al., 2018 ‫به‬ ‫گونه‬ ‫هر‬ ‫تعداد‬ ‫و‬ ‫گرفته‬ ‫قرار‬ ‫شناسایی‬ ‫مورد‬ ) ‫تعداد‬ ‫گونه‬ ‫هر‬ ‫از‬ ‫گردید.‬ ‫ثبت‬ ‫زیستگاهی‬ ‫تکرار‬ ‫هر‬ ‫و‬ ‫ایستگاه‬ ‫هر‬ ‫تفکیک‬ 5 ‫اتانول‬ ‫الکل‬ ‫در‬ ‫غذایی‬ ‫رژیم‬ ‫بررسی‬ ‫جهت‬ ‫نمونه‬ 72 ‫نمونه‬ ‫بقیة‬ ‫و‬ ‫گردید‬ ‫منتقل‬ ‫آزمایشگاه‬ ‫به‬ ‫و‬ ‫شده‬ ‫تثبیت‬ ‫درصد‬ ‫اطمینان‬ ‫از‬ ‫بعد‬ ‫ها‬ ‫رهاس‬ ‫صید،‬ ‫محل‬ ‫همان‬ ‫در‬ ‫فعال،‬ ‫شناي‬ ‫بازیابی‬ ‫از‬ ‫ازي‬ ‫ماهی‬ ‫صید‬ ‫از‬ ‫بعد‬ ‫بالفاصله‬ ‫شدند.‬ ...
Article
Full-text available
Models based on regression analyzes are used to express patterns of abundance and distribution of fish populations in relation to environmental parameters. Therefore, this study was conducted to investigate the habitat suitability indices of Oxynoemacheilus kiabii and O. karunensis from Alk River (sub-basin of Razavar and Karkheh basin). Sampling was done using a hand net in eight stations (each with three replicates). Five habitat variables were measured and recorded, including river width, river depth, bed slope, water velocity, and average bed size. The results showed that the most habitat preference of Kiabi loach is depth in the range of 46-<52 cm, 0.6-<0.9 m width, 5.8-<6.4% slope, and water velocity 0.52-<0.58 m/s and the size of bedrock is 0-<0.12 mm and for O. karunensis was calculated as depth in the range of 10-<16 cm, 2.1-<2.4 m width, 1.6-<2.2% slope, and water velocity 0.34-<4 m/s and the size of bedrock is 48-<60 mm. Also, the highest and lowest SI values for both species O. kiabii and O. karunensis were related to depth and average bed size for O. kiabii and velocity and depth for O. karunensis, respectively. The results showed that Alk River is a suitable habitat for O. karunensis, whereas not suitable habitat for O. kiabii. Examination of the results of their feeding habits and preferences in the digestive system showed that these favorite of fishes are Chironomidae, Simulidae, Baetidae, Gomphidae and Hydropsychidae.
... Since the description of Turcinoemacheilus kosswigi from headwaters of the Greater Zab River in Türkiye by Bănărescu & Nalbant (1964), there had been little attention on this peculiar genus of nemacheilid loaches for about half a century, until Conway et al. (2011) described an additional species, T. himalaya, from Nepal, shortly followed by Golzarianpour et al. (2013) and Esmaeili et al. (2014) describing four new species (T. bahaii, T. hafezi, T. minimus, T. saadii) from the Gulf basin in Iran and Türkiye. ...
Article
Turcinoemacheilus inexpectatus, new species, is described from the Greater Zab, Lesser Zab, and Sirvan drainages, all tributaries of the middle Tigris. It belongs to the T. kosswigi species group. The new species is distinguished from its congeners by an indistinct or prominent midlateral stripe broader than the eye diameter often overlaid by a row of dark-brown blotches, greater pre-pelvic distance, deeper caudal peduncle, and wider interorbital distance.
... Our sampling from the same locality found both Sasanidus kermanshahensis and T. saadii. Golzarianpour et al. [8] described T. hafezi from the Shalamzar stream based on its morphology, but no DNA sequences from the type materials were provided. The original paper included a photo of live specimens of T. ansari (their Figure 5, Beshar River), assigned to T. hafezi. ...
Article
Full-text available
Nemacheilid fishes in the genus Turcinoemacheilus are physically small members of the ichthyofauna communities of high-altitude and mountainous freshwater ecosystems. They are all distributed in Western Asia apart from a single species, described in the Himalayas. They are usually very similar in appearance, which complicates their proper identification and/or description. This is why it is important to use multidisciplinary and integrative taxonomical approaches in order to study their true diversity. In this study, three new species of Turcinoemacheilus are described from Iran, raising the total number of valid species to nine. Turcinoemacheilus ansari new species, is distinguished by the anus being situated behind the midpoint of the pelvic-fin and anal-fin origins and the short anal-fin base length. Turcinoemacheilus christofferi new species, differs by the anus being situated behind the midpoint of the pelvic-fin and anal-fin origins, with a complete lateral line reaching to the anterior part of the caudal fin. Turcinoemacheilus moghbeli new species, is distinguished by the anus being situated at or in front of the midpoint of the pelvic-fin and anal-fin origins, with a great pre-pelvic distance and a caudal peduncle length 1.5–2.3 times its length. In Western Asia, all Turcinoemacheilus species are well separated by molecular characters, showing between 3.6 and 14.1% uncorrected p genetic distances in the COI barcode region. This work shows the importance of studying the hidden diversity of under-sampled and understudied groups of organisms to have a clear image of true biodiversity in order to effectively conserve and protect it.
... Nemacheilus angorae lenkoranensis was described from Lenkoran (also spelled Lankaran) by Abdurakhmanov (1962). It is treated as a species of Oxynoemacheilus by Golzarianpour et al. (2011) and as a synonym of O. bergi by Çiçek et al. (2018) without examination of material or analysis of characters given in the description or shown in the figures. The Lenkoran River, having its estuary at Lenkoran, is a small tributary of the Caspian Sea between the Sefid and the Kura. ...
Article
The Oxynoemacheilus bergianus species group is revised based on tree topology (ML, NJ, MP), distance (K2P and ASAP) and Poisson tree process analyses of DNA barcode data tested against morphometric and morphological characters including colour patterns. The O. bergianus species group is distinguished from other Oxynoemacheilus groups based on morphological characters: its constituent species have a slender caudal peduncle, a suborbital flap in the male, a mottled or blotched colour pattern, and lack bold, black spots on the caudal-fin base. It is also supported as a monophyletic unit in our molecular analysis. The O. bergianus group includes 10 molecular clades following congruently well-supported NJ, MP and ML based entities. Species described as O. bergianus, O. banarescui, O. erdali, O. fatsaensis, O. samanticus, and O. simavicus from Turkey, O. lenkoranensis from Azerbaijan, and O. longipinnis and O. parvinae from Iran belong to this species group. The group includes also four unnamed molecular clades. We were unable to detect external differences between any of the molecular clades in colour pattern or any morphometric or morphological characters examined. In the 10 molecular clades in the O. bergianus species group, the intraclade K2P distance ranges from 0.0-1.8% while the distances between molecular clades ranges from 0.6-5.9%. To resolve the species diversity of this group, we also analysed the intraspecific and interspecific variability in the K2P distance of DNA barcode data from 53 other Oxynoemacheilus species. Here, the intraspecific variability ranges from 0.0-2.4% while the interspecific K2P distance ranges from 1.2-20.8%. In the O. bergianus species group, only four groups are detected by the mPTP species delimitation approach distinguished by a K2P distance of 2.9% or more. We treat these four groups as valid species, corresponding to O. banarescui, O. bergianus, O. fatsaensis, and O. simavicus. Oxynoemacheilus samanticus from the Kızılırmak and Seyhan drainages, O. lenkoranensis from the Caspian basin, O. erdali from the Euphrates, and O. longipinnis and O. parvinae from the Tigris drainage are treated as synonyms of O. bergianus. Fishes from an unnamed molecular clade from the upper Tigris, and from a second unnamed clade from the upper Euphrates, are both identified as O. bergianus. Oxynoemacheilus bergianus might be a junior synonym of O. bergi from the Kura. The distribution range of O. simavicus, described from the Simav drainage in the Marmara basin, is expanded to the east and two molecularly differentiated population groups occur in the Sakarya drainage, the Büyük Melen River and potentially in other adjacent coastal streams. Oxynoemacheilus fatsaensis, described from the coastal stream Elekçi in northern Anatolia, is also widespread in the Yeşilırmak drainage. Morphological characters proposed to distinguish O. fatsaensis from the other species of the O. bergianus group could not be confirmed by our data on fishes from the Yeşilırmak. This study also discusses the theoretical background, our reasons for conducting this revision in the way we did, and what the alternatives would be.
... Erk 'akan and Kuru (1986) described Orthrias angorae kosswigi from the Yildiz Stream, Sivas Province, Kizilirmak Basin, and later was considered as valid subspecies of Oxynoemacheilus angorae kosswigi (Fricke et al. 2019). Since status of the most originally subspecies is raised to the species level (Erk'akan et al. 2007;Prokofiev 2009;Golzarianpour et al. 2011;Erk'akan 2012), this species is considered as an available name of O. kosswigi, distributing in the Kizilirmak and Yeşilirmak basins (Ç içek et al. 2015) (Fig. 4). Banarescu (1968) had described Noemacheilus tigris seyhanensis from the Zamanti River, Seyhan Basin. ...
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Morphometric, meristic and molecular (COI) characters of Oxynoemacheilus kosswigi and O. seyhanensis from the Kizilirmak and Seyhan basin, respectively, examined to understand their taxonomic status, since there was no comparison done with O. seyhanensis when describing O. kosswigi. Based on the examined topotype materials, the character of O. kosswigi is largely overlapped or identical with those of O. seyhanensis. Since no character states were found to distinguish these species, we consider O. kosswigi a junior synonym of O. seyhanensis.
... The Nemacheilid loaches of the genus Oxynoemacheilus are widespread from Albania in the west to the Caucasus and Iran in the east . Oxynoemacheilus has been intensively studied in the Tigris River drainage (Golzarianpour et al. 2011, Kanmangar et al. 2014, Jouladeh-Roudbar et al. 2016, Freyhof 2016, Freyhof & Abdullah 2017, Freyhof & Özuluğ 2017, Freyhof & Geiger 2017, Sayyadzadeh et al. 2016 and recognised 15 species from that area. ...
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The Oxynoemacheilus tigris species group is reviewed, resulting in the recognition of six species, of which two are described herein as new. Oxynoemacheilus tigris is known from the endorheic Qweik River and the Merziman River, which is a tributary of the western Euphrates. Oxynoemacheilus ercisianus is endemic to the endorheic Lake Van basin and O. hazarensis is endemic to Lake Hazar basin in the upper Tigris drainage. Oxynoemacheilus kaynaki is widespread in the Euphrates drainage. The two undescribed species occur in the Euphrates drainage. Oxynoemacheilus arsaniasus, new species, from the Murat River and the upper Karasu (Muş) River drainage, is distinguished from other species of the O. tigris group by having a bold, black, irregularly-shaped bar at the caudal-fin base, an incomplete lateral line and a scaleless body. Oxynoemacheilus muefiti, new species, from the upper Murat River drainage and a tributary to the Atatürk reservoir, is most similar to O. ercisianus, from which it is distinguished by a more slender body and a shallower dorsal adipose crest. According to our molecular data, the Qweik population of O. tigris is suspected to be introgressed by O. namiri from the Orontes drainage. Oxynoemacheilus erdali is identified as a synonym of O. bergianus as we were unable to find differences between the two species.
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The Middle East contains a great diversity of Capoeta species, but their taxonomy remains poorly described. We used mitochondrial history to examine diversity of the algae-scraping cyprinid Capoeta in Iran, applying the species-delimiting approaches General Mixed Yule-Coalescent (GMYC) and Poisson Tree Process (PTP) as well as haplotype network analyses. Using the BEAST program, we also examined temporal divergence patterns of Capoeta. The monophyly of the genus and the existence of three previously described main clades (Mesopotamian, Anatolian-Iranian, and Aralo-Caspian) were confirmed. However, the phylogeny proposed novel taxonomic findings within Capoeta. Results of GMYC, bPTP, and phylogenetic analyses were similar and suggested that species diversity in Iran is currently underestimated. At least four candidate species, Capoeta sp4, Capoeta sp5, Capoeta sp6, and Capoeta sp7, are awaiting description. Capoeta capoeta comprises a species complex with distinct genetic lineages. The divergence times of the three main Capoeta clades are estimated to have occurred around 15.6–12.4 Mya, consistent with a Mio-Pleistocene origin of the diversity of Capoeta in Iran. The changes in Caspian Sea levels associated with climate fluctuations and geomorphological events such as the uplift of the Zagros and Alborz Mountains may account for the complex speciation patterns in Capoeta in Iran.
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Turcinoemacheilus kosswigi (Bănărescu and Nalbant, 1964) was recorded for the first time in Iran from the River Karoun drainage, which belongs to the Euphrates-Tigris drainage. Formerly believed to be an endemic species in the basin of River Tigris, it is now recorded in the upper River Euphrates basin. This extension of its recorded range makes it likely that it has been overlooked in other parts of the Euphrates-Tigris system. The species is distinguished from all other loaches by the pelvic-fin origin in front of the dorsal-fin origin and having the anus closer to the pelvic-fin base than to the anal fin origin.
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Oxynoemacheilus is a species-rich genus of nemacheilid fishes known from Albania eastwards to Central Iran. There are 58 available species-group names and 41 species are recognized here as valid. Four species occur in Europe (O. bureschi, O. merga, O. pindus, O. theophilii) and 38 species are found in Anatolia and the Middle East. Barbatula paucilepis, Cobitis tigris, Nemacheilus tigris cyri, N. namiri, Noemacheilus tigris seyhanensis and Orthrias an-gorae ercisianus recently placed in Paracobitis as well as Nun galilaeus and Seminemacheilus tongiorgii are all transferred to Oxynoemacheilus.
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Silvinichthys leoncitensis, new species, is described from Leoncito National Park in the Andes of Argentina. The new species is distinguished from the other two known congeners by the coloration pattern, consisting of a dark marmorated head and body that fades to a paler color ventrally, the pelvic fin and girdle absent, seven to nine opercular odontodes, 18-28 interopercular odontodes, caudal-fin length 19.9-24.0 % SL, length of dorsal fin base 10.1-13.1 % SL, and head width 13.3-15.9 % SL. Silvinichthys leoncitensis is endemic to the type locality, which is situated in the Andean Cordillera of the San Juan province, Argentina. Silvinichthys leoncitensis is hypothesized to be a sister species of S. bortayro.
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Schistura diminuta, new species, is described from the lower Sekong River, Mekong drainage, Cambodia. It is distinguished from congeners by the following characters: tiny adult body size (maximum known size 19.5 mm SL); lateral line incomplete, with 14-17 pores, terminating on the flank anterior to vertical through pelvic-fin origin; absence of axillary pelvic lobe; processus dentiformis weakly developed; dorsal-fin rays iii-iv.8.i; principal caudal-fin rays 8 + 8 (7 + 7 branched caudal-fin rays); a distinct dark brown spot at centre of caudal-fin base; and 9-10 irregular light brown bars along dorsal body surface.
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About 31 species in eight genera and two families (Nemacheilidae and Cobitidae) are reported from Iran and adjacent countries (i.e., Iraq, Turkey, Afghanistan, and Pakistan). Six new species, five from Iran and one from Afghanistan, are described. Several Iranian loach genera are also found in western Palearctic region (i.e., Sabanejewia, Cobitis, and Orthrias), or eastern Asia (i.e., Schistura). But other genera such as Paracobitis and Seminemacheilus are endemic to, or exclusive of, Middle Asia. Our investigation confirms the important role of Iranian drainages as a biogeographic bridge between western-Palearctic and Oriental fish faunas.
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Rasbora atranus, new species, is described from the upper Mahakam drainage, central Borneo. It belongs to the R. sumatrana-elegans complex (sensu Brittan, 1954). It is distinguished by having a dark midlateral stripe from the operele to the caudal-fin base, often faint or poorly contrasted, widened in a faint elongated triangular blotch at the end of the caudal peduncle; by the presence of a conspicuous oval to triangular black blotch along the anterior half of the anal-fin base; by the fins orange in life. © 2011 by Verlag Dr. Friedrich Pfeil, München, Germany - ISSN 0936-9902.
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Systomus xouthos, new species, is described from Belait and Tutong drainages in Brunei. It is distinguished by the adults having a plain brown body with a blackish reticulate pattern; the juveniles with a faint black spot at dorsal-fin origin and a midlateral series of 3 or 4 black blotches on the flank; a black band across dorsal fin; 12 scale rows around the caudal peduncle; a deeply forked caudal fin with long pointed lobes; and the dorsal and anal fins with a concave posterior margin. Systomus pulcher from eastern Borneo is revalidated from the synonym of S. tetrazona. © 2011 by Verlag Dr. Friedrich Pfeil, München, Germany - ISSN 0936-9902.