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A new species of Parotocinclus (Siluriformes: Loricariidae) from the upper Rio São Francisco, Brazil

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A new species of the hypoptopomatine loricariid Parotocinclus is described based on material from three rivers belonging to the upper and middle Rio São Francico basin, the Rio das Velhas and Rio Jequitaí on the right margin and the Rio Paracatu on the left margin. The new species is readily distinguished from all congeners by having the abdomen completely devoid of dermal plates between the pectoral girdle and the anus, by differences in rostral and postrostral plates, and by having the pectoral girdle covered by skin medially and exposed and supporting odontodes only laterally.
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56 Accepted by M. R. de Carvalho: 20 Apr. 2012; published: 17 Jul.
ZOOTAXA
ISSN 1175-5326 (print edition)
ISSN 1175-5334 (online edition)
Copyright © 2012 · Magnolia Press
Zootaxa 3390: 5664 (2012)
www.mapress.com/zootaxa/Article
A new species of Parotocinclus (Siluriformes: Loricariidae) from the upper
Rio São Francisco, Brazil
PABLO LEHMANN A.¹ & ROBERTO E. REIS²
¹Laboratório de Ictiologia,Universidade do Vale do Rio dos Sinos. Av. Unisinos, 950, 93022-000 São Leopoldo, RS, Brazil.
Email: pablole@unisinos.br
²Laboratório de Sistemática de Vertebrados, Pontifícia Universidade Católica do Rio Grande do Sul, P. O. Box 1429, 90619-900
Porto Alegre, RS, Brazil. E mail: reis@pucrs.br
Abstract
A new species of the hypoptopomatine loricariid Parotocinclus is described based on material from three rivers belonging
to the upper and middle Rio São Francico basin, the Rio das Velhas and Rio Jequitaí on the right margin and the Rio
Paracatu on the left margin. The new species is readily distinguished from all congeners by having the abdomen
completely devoid of dermal plates between the pectoral girdle and the anus, by differences in rostral and postrostral
plates, and by having the pectoral girdle covered by skin medially and exposed and supporting odontodes only laterally.
Key words: Catfishes, Hypoptopomatinae, Neotropical, taxonomy, biogeography, systematics
Introduction
Despite being entirely located on the of the Brazilian Shield, a region with the highest diversity of neoplecotomine
and hypoptopomatine loricariids, the Rio São Francisco basin harbours only a few, rather unrelated species of both
subfamilies. Of the neoplecostomines only Pareiorhaphis mutuca and Neoplecostomus franciscoensis are currently
known and among the hypoptopomatines four species are presently recorded for the entire basin: Otocinclus
xakryaba, Parotocinclus jumbo, P. pr ata and Plesioptopoma curvidens. During the course of an expedition
conducted in the Rio São Francisco basin in 1993 by the Academy of Natural Sciences of Philadelphia (ANSP), the
Museum of Sciences and Technology (MCP), and the Federal University of São Carlos (UFSCar), specimens of a
remarkable new species of Parotocinclus were obtained. Two subsequent expedition (in May 2004 and October
2008) were organized to the area where the first specimens were collected, yielding several new specimens that
allow us to describe the new taxon.
Methods
Measurements and counts follow Carvalho & Reis (2009). Measurements were taken as point-to-point linear
distances with digital calipers under a dissecting scope on the left side of specimens, and recorded to the nearest 0.1
mm. Morphometric data are expressed as percents of standard length (SL), except for subunits of the head, which
are expressed as percents of head length (HL). Plate counts and nomenclature follow the schemes of serial
homology of Schaefer (1997). Vertebral counts include all vertebrae including the five centra modified into the
Weberian apparatus, with the compound caudal centrum (PU1+U1) counted as one element. Vertebral elements
were counted in cleared and stained specimens only. Osteological examinations were performed in specimens
cleared and double stained for bones and cartilages (c&s) prepared according to the technique of Taylor & Van
Dyke (1985).
The specimens examined for this study are deposited in the following institutions: American Museum of
Natural History, New York (AMNH); Academy of Natural Sciences of Philadelphia, Philadelphia (ANSP); Auburn
Zootaxa 3390 © 2012 Magnolia Press · 57
NEW SPECIES OF PAROTOCINCLUS
University Museum, Auburn (AUM); Field Museum of Natural History, Chicago (FMNH); Illinois Natural History
Survey, Urbana-Champaign (INHS); Instituto Nacional de Pesquisas da Amazônia, Manaus (INPA); Museo de
Biologia de la Universidad Central de Venezuela, Caracas (MBUCV); Museo de Ciencias Naturales, Guanare
(MCNG); Museu de Ciências e Tecnologia da Pontifícia Universidade Católica do Rio Grande do Sul, Porto Alegre
(MCP); Museum of Comparative Zoology, Cambridge (MCZ); Museu Nacional, Rio de Janeiro (MNRJ); Museu
de Zoologia da Universidade de São Paulo, São Paulo (MZUSP); Naturhistorisches Museum, Wien (NMW); and
Universidade Federal do Rio Grande do Sul, Porto Alegre (UFRGS).
Results
Parotocinclus robustus, new species
Fig. 1, Table 1
Holotype: MCP 46689, 42.0 mm SL, male, Brazil, Minas Gerais, Bocaiúva, Rio São Francisco basin, creek 45 km
S of Montes Claros on highway BR-135 towards Bocaiuva, Rio Jequitaí basin (17°05’31”S 043°49’48”W), 20 July
1993, R. Reis, J. Silva, E. Pereira & S. Schaefer.
Paratypes: Brazil, Minas Gerais, Rio São Francisco drainage: MCP 16746, 7, 26.5−30.7 mm SL + 1 c&s, 39.3
mm SL (5, 26.5−30.7 mm SL), and ANSP 192455, 3, 29.7−33.9 mm SL, collected with the holotype. MCP 36847,
8, 22.7−29.5 mm SL + 2 c&s, 24.2−29.2 mm SL (8, 22.7−29.5 mm SL), Francisco Dumont, Córrego Diamante on
road from Buriti Grande and the highway BR-135, Rio Jequitaí basin (17°25’53”S 044°07’17”W), 11 October
2004, R. Reis, P. Lehmann & E. Pereira. MCP 23645, 2, 22.3−28.2 mm SL + 1 c&s, 26.2 mm SL (2, 22.3−28.2 mm
SL), Santana do Riacho, Rio Cipó on road from Jabuticatubas to Santana do Riacho, Rio das Velhas basin (approx.
19°12’S 043°43’W), August 1994, F. Vieira, C. B. M. Alves & G. B. Santos. UFRGS 9881, 8, 21.2−30.2 mm SL
(4, 26.7−30.2 mm SL), João Pinheiro, Rio Santo Antônio on highway BR-040 from Canoeiros to João Pinheiros,
Rio Paracatu basin (17°57’37”S 045°42’17”W), 24 May 2008, T. Carvalho & F. Jerep.
Diagnosis. Parotocinclus robustus differs from all its congeners, except P. prata, by having the abdomen
completely devoid of dermal plates between the pectoral girdle and the anus (vs. abdomen varying from fully
covered with dermal plates to just a few plateles near the pectoral-fin axilla or anterior to the anus). From P. prata
it is readily distinguished by having the ventral surface of the head behind the lower lip smooth, without rugosities
in adults (vs. ventral surface of the head behind the lower lip highly rugose in adult specimens; Fig. 2), and by
having the postrostral plate 4 contacting the infraorbitals 3 and 4 (vs. postrostral plate 4 not contacting the
infraorbital series). The new species is also distinguished from most congeners, except P. arandai, P. bahiensis, P.
prata, and P. s pi lu ru s, by having the rostral plate not visible ventrally on the snout tip (vs. rostral plate visible
ventrally on the snout tip). Parotocinclus robustus is further distinguished from most congeners, except P. spilurus,
P. cearensis, P. prata, P. jumbo, P. spilosoma, and P. cesarpintoi, by having the pectoral girdle covered by skin
medially and exposed and supporting odontodes only laterally (vs. pectoral girdle exposed and supporting
odontodes both medially and laterally).
Description. Proportional measurements and counts in Table 1. Adult size medium for members of this genus
(maximum size 42.0 mm in SL). Body stocky, without conspicuous keels. Caudal peduncle vertically oval in cross
section. Dorsal profile of body convex anteriorly, rising from snout to supraoccipital tip, approximately straight
from that point to dorsal-fin origin, slightly concave from dorsal-fin origin to adipose-fin origin, and then
descending to end of caudal peduncle. Greatest body depth at dorsal-fin origin. Least body depth at shallowest part
of caudal peduncle. Ventral profile slightly concave from snout tip to gill opening, slightly elevating posteriorly
along anal-fin base, almost straight along caudal peduncle. Lateral-line canal with pored tube visible from
compound pterotic to penultimate or antepenultimate plate in middle lateral series. Lateral line complete or with
small gap of 1−3 plates after the first 8 pored plates. Mid-dorsal and mid-ventral series of lateral plates incomplete,
terminating 3−5 plates before caudal fin. Dorsal surface of body covered by plates except for small naked area at
opening of swimbladder capsule posteroventrally to compound pterotic. Ventral surface of head and abdomen
naked. Lateral abdominal plates absent between pectoral-fin axilla and pelvic-fin origin. Pectoral girdle covered by
thick skin medially, exposed and supporting odontodes only laterally. Arrector fossa widely open medially, with
ventral expansion of cleithum and coracoid present only laterally.
LEHMANN & REIS
58 · Zootaxa 3390 © 2012 Magnolia Press
TABLE 1. Morphometrics and meristics of Parotocinclus robustus. SD = Standard deviation, n = number of specimens, H =
holotype.
Head deep; broadly round in dorsal view. Interorbital space flat to slightly convex; superior margin of orbit
slightly elevated. Parieto-supraoccipital slightly elevated posterior to orbit. Smaller individuals with two slightly
elevated crests on posterior portion of parieto-supraoccipital and few enlarged, slightly raised odontodes at its
posterior tip; crests and raised odontodes absent in larger specimens. Snout tip with small area of naked skin,
usually connected ventrally to the upper lip. Rostral and anterior postrostral plates without enlarged odontodes; all
odontodes similar in size and shape to those on remaining of head. Preopercle exposed and supporting odontodes
laterally, in front of opercle; canal-bearing lateral cheek plate moderately expanded mesially in triangular tip and
with unbranched canal. Eye small, dorsolaterally placed. Iris with dorsal operculum. Nostrils at posterior terminus
of pair of shallow depressions beginning close to snout tip, ovoid, slightly longer than wide, positioned closer to
anterior margin of orbit than to snout tip. Internareal area slightly elevated. Oral disk roughly circular; lips well
developed, occupying most of ventral surface of head. Lower lip short, not reaching to almost reaching line
between mesial tips of contralateral canal-bearing cheek plates. Both lips densely covered by papillae; lower lip
with larger papillae immediately posterior to dentaries and decreasing in size towards edge. Posterior edge of lower
lip deeply fringed. Maxillary barbel short, mostly adnate to lower lip and with free distal portion smaller than pupil
Paratypes
H n Low High Mean SD
Standard length (mm) 42.0 23 22.3 42.0 28.4 -
Percent of Standard Length
Head length 27.6 23 26.4 29.8 28.4 0.97
Predorsal Length 44.8 23 43.8 48.5 45.9 1.20
Dorsal-fin spine length 22.6 23 19.8 26.2 22.4 1.93
Anal-fin unbranched ray length 18.6 23 14.3 22.0 18.1 1.91
Pectoral-fin spine length 22.6 23 18.8 26.9 22.4 1.76
Pelvic-fin unbranched ray length 18.6 23 15.5 20.6 18.3 1.39
Cleithral width 30.5 23 25.9 31.6 29.1 1.91
Thoracic length 16.7 23 14.5 18.0 16.9 0.91
Abdominal length 21.7 23 17.0 24.6 21.7 1.45
Body depth at dorsal-fin origin 18.8 23 15.2 20.0 18.0 1.29
Caudal-peduncle length 32.4 23 29.0 33.5 31.3 1.09
Caudal-peduncle depth 10.7 23 9.1 10.8 9.9 0.56
Percent of Head Length
Snout Length 68.1 23 61.5 68.1 65.3 1.72
Orbital diameter 17.2 23 17.2 24.3 20.6 1.59
Interorbital width 49.1 23 43.3 51.4 47.2 2.31
Head depth 67.2 23 54.3 67.2 59.5 4.16
Suborbital depth 32.8 23 25.4 32.8 28.7 2.41
Mandibular ramus 13.8 23 13.4 18.6 14.5 1.18
Counts
Left premaxillary teeth 22 23 18 26 22.1 2.04
Right premaxillary teeth 23 23 18 28 22.3 2.16
Left dentary teeth 2423192622.22.03
Right dentary teeth 2323192521.61.90
Left lateral scutes 27 23 24 27 25.0 0.67
Right lateral scutes 27 23 24 27 25.2 0.71
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NEW SPECIES OF PAROTOCINCLUS
diameter. Teeth small and delicate; asymmetrically bifid. Medial cusp large and wide, rounded, lateral cusp small
and pointed, reaching approximately one-third to half-length of medial cusp. Accessory patch of unicuspid teeth on
both premaxilla and dentary bones absent.
FIGURE 1. Holotype of Parotocinclus robustus, MCP 46689, 42.0 mm SL, male. Brazil, Minas Gerais, Bocaiúva, Rio São
Francisco basin, creek 45 km S of Montes Claros on highway BR-135 towards Bocaiuva, Rio Jequitaí basin.
Dorsal fin originating at or slightly anterior to vertical line passing through end of pelvic-fin base. Dorsal fin
short, reaching 5−6 plates behind its base when adpressed. Nuchal plate exposed, not covered by skin. Dorsal-fin
spinelet platelike, trapezoidal in shape, wider than base of dorsal spine. Dorsal-fin locking mechanism non-
functional. Dorsal-fin spine moderately flexible, followed by seven branched rays. Adipose fin present and
LEHMANN & REIS
60 · Zootaxa 3390 © 2012 Magnolia Press
preceeded by 1−2 middorsal, azigous plates. Pectoral fin moderate in size, with slightly curved and flattened spine
and six branched rays, first longest; subsequent branched rays decrease gradually in size. Posterior margin of
pectoral fin straight to slightly round, overlapping one third to half-lenght of pelvic-fin when adpressed. Pectoral-
fin axillary slit absent. Pelvic fin with one unbranched and five branched rays, almost reaching to just passing anal-
fin origin when adpressed. Pelvic-fin unbranched ray slightly depressed and curved, covered with minute
odontodes ventrally and laterally; odontodes on ventral margin strongly turned mesially. Males with low dermal
flap along posterodorsal margin of thickened first pelvic-fin unbranched ray, more conspicuous near base of ray;
absent in females. Anal fin with one unbranched and five branched rays, reaching five plates behind its base when
adpressed. Caudal fin forked to slightly concave; lower lobe slightly longer than upper; one upper unbranched, 14
branched, and one lower unbranched rays. Vertebral centra 28−30 (3 c&s).
Color in alcohol. Ground color of dorsal and lateral surfaces yellowish tan to light brown. Dorsolateral region
of head, snout, predorsal area and most of dorsal and lateral surface of trunk with many dark brown dots, conspicu-
ous in larger specimen (Fig. 1); absent in smaller (Fig. 3). Four irregular and variably conspicuous saddles; first
crossing anterior dorsal-fin base; second immediately posterior to dorsal-fin base; third immediately anterior to
adipose fin, and and fourth between adipose and caudal fins. Saddles broadly conneted laterally to dark brown
stripe that spans from above pectoral-fin base to before end of caudal peduncle. Light stripe from snout tip to each
nostril. Ventral surfaces whitish tan, with scattered patches of dark chromatophores, most concentrated on cheek
and caudal peduncle. Fins mostly unpigmented, except for dark transverse bands; 3−4 in dorsal, 2−3 in pectoral
and 1−2 in pelvic; 1−2 in anal fins. Caudal fin with vertically elongate, squarish dark blotch at base of rays, pre-
ceeded by conspicuous light transverse band at end of caudal peduncle. One of two irregular, sometimes oblicuous,
dark bands on caudal fin, connected to each other by dark pigmentation in central caudal-fin rays.
FIGURE 2. Ventral surface of head of Parotocinclus prata, MCP 28303, 47.7 mm SL, male.
Zootaxa 3390 © 2012 Magnolia Press · 61
NEW SPECIES OF PAROTOCINCLUS
FIGURE 3. Color variation in Parotocinclus robustus, MCP 16746. A—27.0 mm SL, female; and B—28.6 mm SL, female.
FIGURE 4. Drainage map of eastern Brazil showing the distribution of Parotocinclus robustus (dots) and P. p ra ta (squares) in
the upper Rio São Francisco basin. Some symbols represent more than one collecting locality. Open symbol represent the type
locality.
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62 · Zootaxa 3390 © 2012 Magnolia Press
Sexual dimorphism. Males possess the characteristic conical urogenital papilla, positioned just behind the
anal opening. Adult males also possess a low fleshy flap along the dorsal margin of the first thickened pelvic-fin
ray, that is absent in females. The flap is slightly deeper basally and progressively narrows distally. Flap is absent in
juvenile males and females.
Distribution and habitat. Parotocinclus robustus is known from three rivers belonging to the upper and
middle Rio São Francico basin, the Rio das Velhas and Rio Jequitaí on the right margin and the Rio Paracatu on the
left margin, suggesting that the species is widely distributed across the basin (Fig. 4). The type-locality and other
streams where the species was found are small to median-sized rivers with shallow water (0.4−1.5 m depth) and
slow to median-speed waterflow. The streams had clear to slightly turbid water running over a mixed bottom
composed of stones, gravel, sand and sometimes mud. Specimens were mostly collected on the marginal
vegetation.
Etymology. The species epithet robustus is from the Latin, meaning robust, referring to the strong and robust
appearance of the fish. An adjective.
Discussion
The Rio São Francisco basin has only four species of the hypoptopomatines, two of which belonging to
Parotocinclus. Parotocinclus prata is known from the Rio da Prata, a tributary to the left margin of the upper Rio
São Francisco, and P. ju mb o, originally described from several smaller coastal basins in northeastern Brazil, but
also present in the Rio São Francisco basin (see comparative material examined). The new species is apparently
more closely related and chiefly resembles P. prata, both species being probably basal among Parotocinclus and
sister-species to each other. They share a unique feature among all Parotocinclus species of having the abdomen
completely devoid of dermal plates between the pectoral girdle and the anus. On the other hand, they are clearly
distinguished by the ventral surface of head behind the lower lip, which is smooth and without rugosities in adults
of the new species and highly rugose in P. p ra ta (Fig. 2); and by the postrostral plate 4 contacting the infraorbitals
3 and 4 in P. ro bustus and not contacting P. pr at a. In addition, P. prata is a larger species, attaining a maximum size
of 48.7 mm SL (MCP 28303), while the largest adult known of the new species has 42.0 mm SL. Parotocinclus
bahiensis also has the abdomen mostly naked, but as shown by Soares-Sarmento et al. (2009, fig. 2) it has small
platelets on the abdomen surface behind the exposed portion of the pectoral girdle and in the pre-anal region.
A subclade within what is currently know as Parotocinclus is formed by those species inhabiting the Guyana
Shield and the Amazonas and Orinoco basins, that are usually dark colored, small sized, and have a rather pointed
snout. Species in this clade, which is currently being described as a new genus by ourselves (Reis & Lehmann,
2011), are easily distinguished from P. ro bu st us by having (except P. collinsae) a triangular patch of dark
pigmentation on the anterior dorsal-fin base, among other synapomorphies. Parotocinclus collinsae, conversely, is
easily distinguished by having a patch of unicuspid accessory teeth on both the dentary and premaxilla, absent in P.
robustus.
Further on Parotocinclus the Rio São Francisco basin has two additional members of the Hypoptopomatinae,
Otocinclus xakryaba and the recently described (Reis et al., 2012) Plesioptopoma curvidens. The new species is
easily distinguished from both species by having the abdomen completely naked and by possessing an adipose fin,
versus abdomen covered with plates and adipose fin absent in both species.
Comparative material examined. Parotocinclus arandai: MNRJ 28296 (holotype), MCP 43934 (3), MCP
43935 (1 c&s). Parotocinclus aripuanensis: MZUSP 36899 (holotype), MZUSP 36900 (1 paratype), MZUSP
36901 (1 paratype), MZUSP 36902 (1 paratype), MZUSP 36903 (1 paratype) , MZUSP 36904 (1 paratype),
MZUSP 36905 (1 paratype), MZUSP 36906 (1 paratype), MCP 35879 (50 + 4 c&s), MCP 35883(1), MCP 35884
(1), INPA 837 (3), INPA 1134 (2), INPA 1143 (7), INPA 4590 (10), INPA 6674 (4). Parotocinclus bahiesis: MBML
2124 (8), MBML 2147 (2 c&s). Parotocinclus britskii: INHS 31733 (10 + 2 c&s), INHS 49369 (1), ANSP 168171
(13), ANSP 168172 (16), ANSP 179130 (1), ANSP 179131 (5), ANSP 179132 (1), ANSP 179133 (3), ANSP
179134 (1), ANSP 179135 (1), ANSP 179137 (1), ANSP 179138 (15), ANSP 179139 (27), ANSP 179210 (3),
ANSP 179498 (6), AUM 35721 (1), AUM 35722 (4), AUM 35723 (2), AUM 35724 (4), AUM 35725 (20), AUM
35730 (37), AUM 36607 (21), MCNG 43374 (2), MCNG 29463 (12), MCNG 29427 (1), MCNG 29527 (1),
MCNG 16658 (1), MCNG 16476 (13), MCNG 16656 (2), MCNG 929 (1), MCNG 16041 (1), MCP 34708 (5),
Zootaxa 3390 © 2012 Magnolia Press · 63
NEW SPECIES OF PAROTOCINCLUS
MCP 34709 (10). Parotocinclus cearensis: MNRJ 8689 (8 + 2 c&s paratypes), ANSP 69414 (1 paratype).
Parotocinclus cesarpintoi: MNRJ 1022 (3 syntypes), MNRJ 1024 (1 syntype), MNRJ (2 syntypes), MNRJ 1154 (8
+ 2 c&s syntypes), MCP 30562 (11), MCP 31462 (4 + 1 c&s), MCP 31464 (10 + 2 c&s). Parotocinclus collinsae:
AMNH 55433 (holotype), AMNH 55434 (2 of 4 paratypes), ANSP 175923 (1 c&s), ANSP 175927 (1), ANSP
179140 (4), AUM 35577 (10 + 1 c&s), MCP 34710 (3). Parotocinclus cristatus: MNRJ 10132 (holotype), MNRJ
10120-10126 (4 paratypes), MCP 17827 (2 + 1 c&s), MCP 18087 (15), MCP 18091 (20), MCP 18116 (31 + 2
c&s), MCP 19091 (20), MCP 34659 (5), MCP 34660 (2), MCP 34670 (2), MCP 36813 (10 + 2 c&s), ANSP
174135 (25). Parotocinclus doceanus: MZUSP 2698 (1 paratype), MZUSP 8059 (1 paratype), MZUSP 8060 (1
paratype), ANSP 174126 (12), ANSP 174127 (10 + 2 c&s), MCP 18084 (16 + 2 c&s), 18088 (3), 17828 (1).
Parotocinclus eppleyi: ANSP 160700 (5 + 1 c&s paratypes), ANSP 165845 (11 + 2 c&s paratypes), ANSP 165846
(1 paratype), ANSP 169470 (8 paratypes), MCP 33313 (10 paraypes, formerly MBUCV-V-22524), AUM
22338(2), AUM 22635 (6), FMNH 85863 (1), FMNH 103541 (40 of 162), FMNH 108763 (1), MCNG 3010 (3 of
4), MCNG 6957 (15 of 111), MCNG 21655 (1), MCNG 21698(3), MCNG 22184 (1), MCNG 22306 (1), MCNG
23323 (3), MCNG 23591 (2), MCNG 25886 (1), MCNG 26630 (20 of 30), MCNG 33131 (4 + 1 c&s), MCNG
34147 (2), MCNG 39512 (13), MCNG 41450 (3), MCNG 41460 (3), MCNG 44274 (3). Parotocinclus haroldoi:
MNRJ 10536 (1 paratype), MNRJ 10535 (1 paratype), MNRJ 11383 (5 + 3 c&s paratypes), FMNH 71345 (3).
Parotocinclus jimi: MZUSP 12133 (holotype), MZUSP 12134, 12135, 12141, 12144, 12153 (5 paratypes),
MZUSP 12154 (17 + 2 c&s paratypes), MCP 17876 (2), MCP 33329 (3 + 1 c&s), MCP 36830 (3), MCP 36934 (8).
Parotocinclus jumbo: MCP 12829 (2 + 1c&s), MCP 30563 (42), MCP 30688 (1), MCP 30914 (107 + 2 c&s), MCP
31107 (87 + 4 c&s). Parotocinclus longirostris: MZUSP 36891 (holotype), MZUSP 36892 (1 paratype), MZUSP
36893 (1 paratype), MZUSP 36894 (1 paratype). Parotocinclus maculicauda: NMW 45380 (1 paralectotype),
NMW 45381(1 paralectotype), MCZ 89082 (2 paralectotypes), MCP 10990 (35 + 2 c&s), MCP 17605 (3 + 2 c&s),
MCP 20075 (4 + 2 c&s), MCP 20077 (11), MCP 29086 (17 + 2 c&s), MCP 31591 (50 + 4 c&s), MCP 11544 (6),
MCP 11549 (4), MCP 12550 (1), MCP 16501 (2), MCP 16524 (2), MCP 16539 (1), MCP 16571 (1), MCP 16573
(3), MCP 16600 (3), MCP 17605 (5), MCP 17525 (5), MCP 17613 (18), MCP 20074 (5), MCP 20087 (17), MCP
20088 (2), MCP 20089 (1), MCP 20091 (1), MCP 20104 (18), MCP 20106 (5), MCP 20119 (3), MCP 22334 (4),
MCP 22335 (51), MCP 26133 (1), MCP 29086 (19), MCP 29094 (17), MCP 31589 (1), MCP 34455 (1), MNRJ
13745 (18 + 2 c&s), MNRJ 14845(20), MNRJ 13736 (10). Parotocinclus minutus: MNRJ 10135 (holotype), MNRJ
10133, 10134 (2 paratypes), MCP 40034 (8 + 2 c&s). Parotocinclus prata: MCP 28322 (17 + 1 c&s), MCP 27381
(4 paratypes), MCP 28303 (44 + 2 c&s), MCP 28320 (7), MCP 28322 (19), MCP 28325 (1), MCP 28326 (2), MCP
28327 (1), MCP 28335 (11), MCP 28341 (11), MCP 28346 (16), MCP 34234 (11), MZUSP 42205 (27 + 3 c&s).
Parotocinclus planicauda: MCP 27321 (1 + 1 c&s), MCP 27342 (1), MCP 31313 (1), MCP 31317 (8 + 2 c&s),
MCP 31341 (1), MCP 31342 (15), MCP 34370 (8), MCP 34397 (21). Parotocinclus polyochrus: AMNH 74482
(holotype), AMNH 77520 (1 paratype), INPA 15885 (1 + 1 c&s). Parotocinclus spilosoma: ANSP 69410
(holotype), ANSP 69417 (24 paratypes), AUM 20581 (26 + 2 c&s), AUM 28636 (1), AUM 28663 (1).
Parotocinclus spilurus: ANSP 69403 (holotype), ANSP 69404 (4 + 1 c&s paratypes).
Acknowledgements
We would like to thank Edson H. L. Pereira, Tiago P. Carvalho and Fernando C. Jerep for helping in the field and
collecting specimens of the new species. We also thank Fábio Vieira, Carlos B. M. Alves and G. B. Santos for the
long term collaborations in sending us specimens of loricariids. We are grateful to M. Lucena and C. Lucena for
support at the MCP fish collection and Vivianne B. Sant´Anna for helping with the map. This paper was financially
supported by the “All Catfishes Species Inventory” Project (NSF DEB 0315963) that provided funding fieldwork.
RER is partially funded by the Conselho Nacional de Desenvolvimento Científico e Tecnológico—CNPq (process
#303362/2007-3).
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64 · Zootaxa 3390 © 2012 Magnolia Press
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(Siluriformes: Loricariidae) from northern South America. Abstracts of the 2011 meetings of the American Society of
Ichthyologists and Herpetologists, Minneapolis, USA.
Reis, R.E., Pereira, E.H.L. & Lehmann, P. (2012) A new genus and species of hypoptopomatine catfish (Siluriformes,
Loricariidae), from the upper Rio São Francisco basin, Brazil. Copeia, 2012(1), 6–11.
Schaefer, S.A. (1997) The Neotropical cascudinhos: Systematics and biogeography of the Otocinclus catfishes (Siluriformes:
Loricariidae). Proceedings of the Academy of Natural Sciences of Philadelphia, 148, 1–120.
Soares-Sarmento, L.M., Lehmann, P. & Martins-Pinheiro, R.F. (2009) Parotocinclus arandai, a new species of
hypoptopomatine catfish (Siluriformes: Loricariidae) from the upper rio Jucuruçu and Buranhém, states of Bahia and
Minas Gerais, Brazil. Neotropical Ichthyology, 7, 191–198,
Taylor, W.R. & Van Dyke, G.C. (1985) Revised procedures for staining and clearing small fishes and other vertebrates for bone
and cartilage study. Cybium, 9, 107–119.
... Parotocinclus is the most diverse genus of the subfamily, and in the last decade a total of 14 species were described, more than one species per year, encompassing 38 species of the genus (Fricke et al., 2021;Lehmann et al., 2020;Lehmann & Reis, 2012;Pereira et al., 2019;Silva-Junior et al., 2020). Currently, 21 valid species are registered in freshwater ecoregions that drain the north-east, approximately 56% of those described for the genus to date (Fricke et al., 2021;Lima et al., 2017). ...
... The morphological, morphometric and meristic data of species not included in the Comparative Material Examined section used for comparisons were extracted from original description and redescription studies of the species (Boeseman, 1974;Gauger & Buckup, 2005;Lehmann et al., 2015Lehmann et al., , 2018Lehmann et al., , 2020Lehmann & Reis, 2012;Pereira et al., 2019;Roxo et al., 2016Roxo et al., , 2017Roxo et al., , 2019bSchaefer, 1988;Schaefer & Provenzano, 1993;Schmidt & Ferraris Jr, 1985). ...
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A new species of Parotocinclus is described from the Rio Mamanguape basin, in the State of Paraíba, Northeastern Brazil. The new species can be distinguished from all of its congeners, except for P. bahiensis, P. cesarpintoi, P. jumbo, P. nandae and P. spilosoma, by the presence of an abdomen covered by a few small and dispersed platelets (vs. an abdomen entirely covered by large plates in adult individuals or the absence of plates in that region). The new species differs from those mentioned above with respect to several features, such as an exposed pectoral girdle and supporting odontodes medially and laterally; the number of premaxillary and dentary teeth; odontodes covering only the lateral portion of the cleithrum and the absence of irregular golden lines on the head and body (colour in vivo). The new species was collected only in the upper and middle portions of the Rio Mamanguape basin, suggesting a geographic distribution restricted to the Caatinga biome. This article is protected by copyright. All rights reserved.
... Although the genus has been shown to be nonmonophyletic by both morphology-based (Gauger and Buckup, 2005;Lehmann et al., 2013) and molecular studies (Cramer et al., 2011;Roxo et al., 2014), species of Parotocinclus from the Amazon, Orinoco, and the coastal drainages of the Guianas do form a clade. This clade is diagnosed by the canal cheek plate on the ventral surface of the head being posteriorly elongated and contacting the anterior margin of the cleithrum (Lehmann and Reis, 2012;Lehmann et al., 2014Lehmann et al., , 2015Lehmann et al., , 2018. This clade includes species that have more elongated and generally pointed snouts, like P. collinsae (Essequibo River, Guyana), P. eppleyi (Río Orinoco, Venezuela), P. halbothi (Trombetas River, Brazil and Marowijne River, Suriname), P. longirostris (middle Amazon River, Brazil), P. polyochrus (Casiquiare, Venezuela), P. variola (upper Amazon River, Colombia), and P. yaka (Tiquié River, upper Negro basin, Brazil), as well as species with more rounded and not very elongated snouts, like Parotocinclus amazonensis (lower Amazon Basin), P. aripuanensis (lower Madeira Basin), and P. britskii (Guyana, eastern Venezuela, and Roraima State, Brazil). ...
... Conservation status of the new species was assessed following the categories and criteria of the International Union for Conservation of Nature (IUCN Standards and Petitions Subcommittee, 2019). Comparative material examined is listed in Lehmann and Reis (2012) and Lehmann et al. (2014Lehmann et al. ( , 2015Lehmann et al. ( , 2018. Paratypes.-All ...
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Parotocinclus kwarup, new species, is described as a new hypoptopomatine cascudinho from tributaries of the upper Xingu River in the Amazon basin of Brazil. The new species is distinguished from its congeners in northeastern and southeastern Brazil by having the cheek canal plate elongated posteriorly on the ventral surface of the head and in contact with the cleithrum. Parotocinclus kwarup, new species, is diagnosed from other species of Parotocinclus in the Amazon, Orinoco, and Guianas watersheds by the number of oral teeth, the snout length, having odontodes on the ventral surface of the first pelvic-fin ray bent and pointing mesially, lacking a Y-shaped light marking dorsally on the head (from the posterodorsal margin of orbit to posterior parieto-supraoccipital tip), lacking premaxillary and dentary accessory teeth, and having an adipose fin. The extinction risk of the new species is preliminarily assessed as Least Concern based on its wide distribution area and its inferred presence in the large Xingu Indigenous Park.
... Permission for collecting was granted by ICMBio # 13754-1. Comparative material of Parotocinclus species used herein are those listed in Lehmann [9], Lehmann & Reis [25], and Lehmann et al. [26]. Counts and measurements followed Lehmann et al. [6]. ...
... Parotocinclus nandae is morphologically most similar to P. adamanteus, P. doceanus, P. jimi, and P. maculicauda in a series of features, including the shared standard length similar (max. 60 mm), number of vertebrae (28)(29)(30), plates in median lateral series (24)(25)(26)(27), and plates between anal and caudal fins (11)(12). However, the new species is easily distinguished from (Fowler, 1941), with the rostral plate exposed ventrally and visible on snout tip), and by the pectoral girdle covered by thick skin medially and exposed supporting odontodes only laterally, restricted to coracoid (except for P. adamanteus, P. jequi, and P. prata, with the pectoral girdle exposed and supporting odontodes medially and laterally). ...
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A new species of Parotocinclus from the upper Rio Paraguaçu, Bahia, Brazil, is described. The new species is distinguished from all congeners by its unique color pattern, with irregular dark blotches resulting in a somewhat marble-spotted pattern on head and trunk of most specimens and dorsum of head with a conspicuous V-shaped light mark from tip of snout to nares. The new species is also distinguished from congeners by having the lower lip elongated posteriorly and reaching or surpassing the anterior margin of cleithrum on the pectoral girdle, the canal cheek plate on the ventral surface of the head reduced and with a slightly concave margin, and abdomen covered by small embedded platelets, without contact with each other and not arranged in a line between the pectoral-fin axilla and pelvic-fin origin. The presence of a thick and rough skin in the interradial membrane of pelvic fin exclusively in the females of P. nandae is reported by the first time to occurs in Siluriformes.
... The genus Parotocinclus Eigenmann & Eigenmann, 1889 is one of the most speciose genera in the loricariid subfamily Hypoptopomatinae, comprising 32 valid species (Eschmeyer et al., 2018). Parotocinclus is widely distributed across cis-Andean South America, and has been divided into two geographically isolated and morphologically distinct species groups (Lehmann & Reis, 2012;Lehmann et al., 2014;Lehmann et al., 2015). Species inhabiting the coastal drainages of the Brazilian Shield from south to northeastern Brazil form a nonmonophyletic assemblage, rather variable in shape, and with the canal cheek plate on the ventral surface of the head rounded, not expanded posteriorly and not contacting the cleithrum. ...
... Specimens examined belong to fish collections which acronyms are listed in Sabaj (2016). Comparative material examined is listed in Lehmann & Reis (2012), Lehmann et al. (2014;2015). Specimens were cleared and stained (c&s) for inspection of bones and cartilages following Taylor & Van Dyke (1985). ...
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Parotocinclus yaka is described as a new species of hypoptopomatine cascudinho from tributaries of the Rio Tiquié, tributary to the Rio Uaupés, upper Rio Negro drainage, Amazon basin, Amazonas State, Brazil. The new species is distinguished from its congeners in northeastern and southeastern Brazil by having the cheek canal plate elongated posteriorly on the ventral surface of the head and in contact with the cleithrum. Parotocinclus yaka is diagnosed from the Parotocinclus species of the Amazon, Orinoco and Guianas watersheds by having a conspicuous dark spots smaller than the pupil diameter distributed dorsally and laterally on the head; it is also differentiated from P. polyochrus (Casiquiare, Venezuela), P. longirostris (Rio Amazonas, Brazil), and P. eppleyi (Río Orinoco) by the absence of a Y-shaped light mark dorsally on the head. In addition, the absence of premaxillary and dentary accessory teeth and the presence of a Y-shaped spot on the snout distinguish the new species from P. collinsae (Essequibo River, Guyana), P. halbothi (Rio Trombetas, Brazil and Marowijne River, Suriname) and P. variola (Río Amazonas, Colombia). Parotocinclus yaka also differs from P. amazonensis (lower Amazon basin), P. aripuanensis (lower Amazon basin), P. britskii (Guyana, Suriname, eastern Venezuela, and Amapá State, Brazil), and P. dani (Rio Tapajós basin), by having more numerous oral teeth. The new species described herein is part of the group of small cascudinhos usually associated with marginal or submerged vegetation and submerged logs, of moderate current and clear transparency, found in conserved habitats in streams of the Amazon, Orinoco and Guianas rivers.
... Institutional abbreviations follow . Comparisons with species not cited in the "Comparative material examined" were based on the literature information (i.e., Gauger & Buckup, 2005;Lehmann et al., 2014Lehmann et al., , 2015Lehmann et al., , 2018Lehmann & Reis, 2012;Pereira et al., 2019;Roxo et al., 2016Roxo et al., , 2017Roxo et al., , 2019Schaefer, 1988;Schaefer & Provenzano, 1993). ...
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A new species of Parotocinclus is described from lower rio Pardo basin, Bahia, Brazil. The new species differs from the majority of its congeners by the presence of a rudimentary or vestigial adipose fin, restricted to 1–3 small unpaired plates on the typical location of the fin. The new species differs from congeners that lack a well‐developed adipose fin, and also from various other congeners, by a series of features including the absence of unicuspid accessory teeth and abdomen completely covered by plates similar in size. Additionally, mature males of the new species possess hypertrophied and higher number of olfactory lamellae, when compared to similar sized or even larger females. Hypertrophied and higher number of olfactory lamellae in males is shared with the congeners from the Northeastern Mata Atlântica freshwater ecoregion examined to the feature. This article is protected by copyright. All rights reserved.
... T HE genus Parotocinclus is widely distributed across cis-Andean South America, and has been demonstrated to be composed of two geographically isolated and morphologically distinct species groups (Lehmann and Reis, 2012;Lehmann et al., 2014Lehmann et al., , 2015. Species living in coastal drainages of the Brazilian Shield from Santa Catarina State of Brazil, in the south, to Piauí State, in the north, compose a possibly non-monophyletic, phenotypically variable group of species where the canal cheek plate on the ventral surface of the head is rounded and not expanded posteriorly to contact the pectoral girdle. ...
... Comparative material examined is that listed in Lehmann and Reis (2012) with the addition of the following specimens (all from Brazil, except where noted). ...
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Parotocinclus adamanteus, new species, is described from a series of specimens collected in the upper portion of the Rio Paraguaçu basin, a coastal river within the Chapada Diamantina domain, a large plateau on the State of Bahia in northeastern Brazil. The description of this new species represents the first record of a member of the Hypoptopomatinae from this relictual area. The new species is diagnosed from other Parotocinclus by having a distinct rostral border forming a fleshy intumescence on the lateral portion of head ornamented with moderately hypertrophied odontodes in adult males. It is also diagnosed from congeners by a remarkable secondary sexual dimorphism in the shape of the pelvic fin, in which the branched rays of males decrease in size, resulting in a pointed posterior fin margin (branched pelvic-fin rays in females have approximately the same size, producing a round posterior fin margin). In addition, the new species can be further distinguished from other species of Parotocinclus by lacking a rostral plate covering the tip of the mesethmoid anteriorly, by lacking abdominal plates between the pectoral girdle and the anus, by having numerous premaxillary teeth (45–61), and by having a short and mesially expanded ventral portion of the cheek canal plate. Recent phylogenetic analysis indicates that Parotocinclus adamanteus, new species, is closely related to P. jequi, P. prata, and P. robustus.
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A new genus of Hypopopomatinae armored catfish is described from the northern portions of South America, namely the Amazon, Orinoco and Guianan coastal drainages. The new genus is diagnosed from all remaining hypoptopomatines by having the canal cheek plate on the ventral surface of the head posteriorly elongated and contacting the cleithrum, in addition to other features that distinguish the new genus from specific genera. Five new species are described and 18 species currently allocated in Parotocinclus, Hisonotus, and Curculionichthys are transferred to the new genus and rediagnosed. Parotocinclus amazonensis and P. aripuanensis are considered junior synonyms of P. britskii. The secondary sexual dimorphism of the members of the new genus is detailed and illustrated. Morphological characters are used to delimit four phenotypic groups of species that might have phylogenetic significance, which still have to be properly tested. A key to the species is offered and diagnoses, illustrations, and distribution maps are provided for all species.
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A new species of Parotocinclus, apparently endemic to the rio Jacuípe basin, Bahia State, Brazil, is described. The new species is distinguished from congeners, except P. bidentatus, P. cabessadecuia, P. dani, P. halbothi, P. muriaensis, P. pentakelis, P. seridoensis, and P. spilurus, by the presence of a reduced adipose fin. The new species differs from the aforementioned species by the absence of unicuspid accessory teeth, abdomen with broad naked areas between lateral and medial patches of plates, and snout tip completely covered by plates and odontodes. The adipose fin of the new species is restrict solely to the adipose-fin spine, lacking the adipose-fin membrane, a reduction pattern previously described to P. halbothi, a congener from rivers of the Amazonas and Marowijne basins.
Article
Neotropical freshwaters host more than 6000 fish species, of which 983 are suckermouth armored catfishes of the family Loricariidae – the most-diverse catfish family and fifth most species-rich vertebrate family on Earth. Given their diversity and ubiquitous distribution across many habitat types, loricariids are an excellent system in which to investigate factors that create and maintain Neotropical fish diversity, yet robust phylogenies needed to support such ecological and evolutionary studies are lacking. We sought to buttress the systematic understanding of loricariid catfishes by generating a genome-scale data set (1041 loci, 328,330 bp) for 140 species spanning 75 genera and five of six previously proposed subfamilies. Both maximum likelihood and Bayesian analyses strongly supported the monophyly of Loricariidae. Our results also reinforced the established backbone of loricariid interrelationships: Delturinae as sister to all other analyzed loricariids, with subfamily Rhinelepinae diverging next, followed by Loricariinae sister to Hypostominae + Hypoptopomatinae. Previous DNA-based relationships within Hypostominae and Loricariinae were strongly supported. However, we evaluated for the first time DNA-based relationships among many Hypoptopomatinae genera and found significant differences with this subfamily's current genus-level classification, prompting several taxonomic changes. Finally, we placed our topological results within a fossil-calibrated temporal context indicating that early Loricariidae diversification occurred across the Cretaceous-Paleogene boundary ∼65 million years ago (Ma). Our study lays a strong foundation for future research to focus on relationships among species and the macroevolutionary processes affecting loricariid diversification rates and patterns.
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Four new species of Hisonotus are described from the upper course of the rio Uruguay basin in Brazil: Hisonotus iota from the rio Chapecó drainage; Hisonotus leucophrys from rio Rancho Grande and rio Ariranhas; Hisonotus megaloplax from the rio Passo Fundo drainage; and Hisonotus montanus from the rio Canoas drainage. The species Epactionotus aky, described from the arroyo Yabotí-Guazú drainage in Argentina, is transferred to Hisonotus and rediagnosed. Hisonotus candombe is considered a junior synonym of H. ringueleti. The new taxa, together with H. nigricauda, H. ringueleti, H. charrua, and H. aky represent the genus Hisonotus in the rio Uruguay basin. A taxonomic key for Hisonotus in the rio Uruguay basin is provided. Their distributions are discussed under biogeographic patterns previously proposed for the rio Uruguay basin.
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Parotocinclus arandai, new species of the hypoptopomatine catfish, is described from small creeks in the upper rios Jucuruçu and Buranhém basins, at the border of Brazilian States of Bahia and Minas Gerais. Parotocinclus arandai is distinguished from all congeners from the Atlantic coastal basins of southeastern and eastern Brazil, except Parotocinclus bahiensis, by having the branched rays and interradial membranes of the pectoral and pelvic fins unpigmented in ventral view. The new species is distinguished from most Parotocinclus species, by having a small eye, 14.8-19.3 mm HL (except P. maculicauda and P. planicauda) and by the presence of a tuft of hypertrophied odontodes on the supraoccipital (except P. cristatus and P. cesarpintoi). Parotocinclus arandai is further distinguished by having an abdomen extensively naked, with a mosaic of few rounded platelets of irregular size and distributed over the pre-anal region (except P. bahiensis, P. minutus, P. spilosoma, P. cearensis, P. cesarpintoi and P. prata). A detailed comparison with congeners on eastern Brazil hydrographical region is provided, and information on the species habitat is given.
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Otocinclus arnoldi from the La Plata basin is resurrected from the synonymy of O. flexilis described from the rio Jacuí drainage, based on three distinguishing features: the possession of five branched pectoral-fin rays, the larger number of enlarged odontodes on the tip of the parieto-supraoccipital posterior process, and having the prootic involved in the contact with the hyomandibular articular condyle. These species are also compared to O. mimulus, a third species described from the Paraná River basin, and the three species are rediagnosed. A reassessment of the phylogenetic relationships of all species of Otocinclus shows a well-supported clade composed of (O. xakriaba ((O. mimulus, O. arnoldi) (O. affinis, O. flexilis))) from the eastern-draining river basins of the Brazilian Shield as sister-group to a clade including all remaining Otocinclus species which are distributed on a wide lowland area of the Amazonas, Paraguay, and Orinoco basins.
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A new, uniquely colored species of the loricariid catfish genus Otocinclus, O. cocama is described from a tributary to the lower río Ucayali in northern Peru. The new species is distinguished from other Otocinclus species by two putatively autapomorphic features, the distinct color pattern, consisting of vertically elongated blotches spanning from the dorsal midline to the ventral border of flanks, and by a complete lateral line. The phylogenetic relationships of the new species are investigated and it is apparently more closely related to a clade formed by O. huaorani, O. bororo, O. mariae, and O. mura. Comments on the impact of taxonomic revisions for the discovery and description of previously undetected biodiversity are also presented. Uma nova espécie de bagre loricariídeo de coloração única do gênero Otocinclus, O. cocama, é descrita de um afluente do baixo río Ucayali no norte do Peru. A nova espécie se distingue das demais espécies de Otocinclus por dois caracteres supostamente autopomórficos, o padrão de coloração diferenciado, que consiste em marcas alongadas verticalmente desde a linha média dorsal até a porção ventral dos flancos, e por uma linha lateral completa. As relações filogenéticas da nova espécie são investigadas e ela é aparentemente mais proximamente relacionada ao clado formado por O. huaorani, O. bororo, O. mariae e O. mura. Ao final, são apresentados comentários sobre o impacto de revisões taxonômicas no descobrimento e descrição de biodiversidade previamente não detectada.
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Plesioptopoma curvidens is a new genus and species of hypoptopomatine loricariid from the upper Rio Paraopeba, a tributary to the Rio São Francisco in southeastern Brazil. Plesioptopoma is attributed to the hypoptopomatines based on five shared synapomorphies, and differs from all remaining members of the subfamily by having the premaxilla and dentary tooth series strongly curved mesially, in such a way that the mesial portion of the tooth series in both sides are turned and run parallel to each other, the caudal peduncle distinctly quadrangular in cross-section, and the anterior margin of the snout devoid of dermal plates.
Article
The genus Otocinclus Cope (1872) of the siluriform family Loricariidae is diagnosed as monophyletic on the basis of shared derived characters of the cranial and hyobranchial skeleton, dorsal gill arch musculature, and gut. Otocinclus are relatively small herbivorous catfishes restricted to small streams and quiet slow-flowing margins of larger rivers, most frequently living in close association with aquatic macrophytes and terrestrial marginal grasses extending into the water column. Otocinclus species share a novel modification of the distal esophageal wall which is developed into an accessory blind diverticulum that may function in aerial respiration and for providing additional modulatory positive buoyancy for remaining in the upper water column at stream margins. Otocinclus has no junior synonyms, however several nominal species originally described in Otocinclus are here formally re-assigned to other genera in the subfamily Hypoptopomatinae. Otocinclus cephalacanthus Ribeiro 1911, O. depressicauda Ribeiro 1918, O. francirochai Ihering 1928, O. laevior Cope 1894, O. leptochilus Cope 1894, O. maculipinnis Regan 1904, O. nigricauda Boulenger 1891, and O. paulinus Regan 1908 are all placed in the genus Microlepidogaster Eigenmann & Eigenmann 1889; O. obtusos Ribeiro 1911 was placed in Pseudotothyris Britski & Garavello 1984; the genus Nannoptopoma Schaefer 1996 was erected for O. spectabilis Eigenmann 1914 in the tribe Hypoptopomatini; O. gibbosus Ribeiro 1908 is removed from Otocinclus, yet remains of undetermined generic status. Thirteen species are recognized in Otocinclus: O. affinis Steindachner 1877 of the lower Paraná/Paraguay and Uruguay basins and coastal streams of southeastern Brazil; O. bororo n. sp. of the upper Río Paraguay; O. caxarari n. sp. of the middle Río Guaporé/Mamoré system; O. flexilis Cope 1894 of the lower Paraná/Paraguay and Uruguay basins and coastal streams of southeastern Brazil; O. hasemani Steindachner 1915 of northern Brazil; O. hoppei Ribeiro 1939 of the upper Amazon, Tocantins and Paraguay basins and coastal streams of northeastern Brazil; O. huaorani n. sp. of the upper Amazon and Orinoco basins; O. macrospilus Eigenmann & Allen 1942 of the upper Amazon basin of Colombia, Ecuador, and Peru; O. mariae Fowler 1940 of the lower Amazon, upper Madeira and Paraguay basins; O. mura n. sp. of the middle Amazon River; O. vestitus Cope 1872 of the upper Amazon and lower Paraná basins; O. vittatus Regan 1904 of the Amazon, Orinoco, Paraná/Paraguay, and Tocantins basins; and O. xakriaba n. sp. of the rio São Fransisco basin. Two species are placed in synonymy: Otocinclus arnoldi Regan 1909 and O. fimbriatus Cope 1894 are junior synonyms of O. flexilis. Keys to the species of Otocinclus and genera of the Hypoptopomatinae are provided. A descriptive treatment of the osteology and cranial myology is provided for O. vittatus. Detailed analysis of meristic and morphometric variation based on geometric morphometric procedures is provided for the phenetically similar species pairs O. mariae and O. vittatus, O. bororo and O. huaorani in an a posteriori evaluation of separate species status. The phylogenetic relationships among Otocinclus species, and the phylogenetic position of Otocinclus among genera of the Hypoptopomatinae, are determined based on analysis of 27 morphological features using cladistic parsimony. Monophyly of Otocinclus was confirmed; within Otocinclus, a clade comprised of O. affinis and O. flexilis is the sister-group to the remainder of the genus. Within that latter clade, O. hasemani and O. xakriaba are the first and second-level sister-groups to the remainder of the genus, within which relationships among species are not fully resolved with available data. The phylogenetic biogeography of Otocinclus is informative regarding the historical relationships among major river drainage basins, particularly of those river systems of the Brazilian Shield. A biogeographic hypothesis is proposed based on the area cladogram derived from the species-level phylogenetic relationships, which suggests successive vicariance and speciation in the non-Amazonian regions of endemism of southeastern and eastern South America, followed by speciation and dispersal within the Amazon, Orinoco and upper Paraguay basins. The pattern of vicariance revealed by the Otocinclus species-level phylogeny is congruent with the geologic history of the major river drainage basins of the Brazilian Shield. This result suggests that, for Otocinclus and perhaps other loricariid catfishes, much of their generic and species-level diversification occurred prior to the formation of the Amazon basin.
ANSP 160700 (5 + 1 c&s paratypes)
  • Parotocinclus Eppleyi
Parotocinclus eppleyi: ANSP 160700 (5 + 1 c&s paratypes), ANSP 165845 (11 + 2 c&s paratypes), ANSP 165846
A new genus and five new species of cascudinhos of the subfamily Hypoptopomatinae (Siluriformes: Loricariidae) from northern South America. Abstracts of the
  • R E Reis
  • P Lehmann
Reis, R.E. & Lehmann, P. (2011) A new genus and five new species of cascudinhos of the subfamily Hypoptopomatinae (Siluriformes: Loricariidae) from northern South America. Abstracts of the 2011 meetings of the American Society of Ichthyologists and Herpetologists, Minneapolis, USA.