A new unicuspid-toothed species of Hypostomus Lacépède, 1803 (Siluriformes: Loricariidae) from the rio Paraguai basin

Claudio H. Zawadzki Luiz F. C. Tencatt Otávio Froehlich About the authors

Abstracts

A new unicuspid-toothed armored catfish species of Hypostomus is described from the Bodoquena Plateau, rio Paraguai basin, Mato Grosso do Sul State, Brazil. The new species is distinguished from its congeners, with exception of H. fonchii, by having unicuspid teeth (vs. bicuspid teeth); from H. fonchii it is distinguished by having median series of lateral plates with 26-27 (vs. 28); by lower number of premaxillary and dentary teeth (7-10 vs. 18-21; 8-13 vs. 18-25, respectively); for possessing more depressed head (head depth 15.8-18.1% SL vs. 19.1-22.0% SL); and by the presence of median buccal papilla (vs. absence).

Armored catfish; Bodoquena Plateau; Cascudo; Hypostominae; Taxonomy


Uma espécie nova de cascudo do gênero Hypostomus com dentes unicuspidados é descrita da Serra da Bodoquena, bacia do rio Paraguai, estado do Mato Grosso do Sul, Brasil. A espécie nova é distinta de suas congêneres, com exceção de H. fonchii, pela presença de dentes unicuspidados (vs. bicuspidados); de H. fonchii é distinta por apresentar a série mediana de placas laterais com 26-27 (vs. 28); pelo menor número de dentes pré-maxilares e no dentário (7-10 vs. 18-21; 8-13 vs. 18-25, respectivamente); por possuir cabeça mais deprimida (altura da cabeça 15.8-18.1% CP vs. 19.1-22.0% CP) e pela presença de papilas bucais medianas (vs.ausência).

Armored catfish; Bodoquena Plateau; Cascudo; Hypostominae; Taxonomy


Introduction

Hypostomus Lacépède is the most species-rich genus of the Loricariidae, which currently comprises 130 valid species (Garavello , 2012Garavello, J. C. , H. A. Britski & C. H. Zawadzki. 2012. The cascudos of the genus Hypostomus Lacépède (Ostariophysi: Loricariidae) from the rio Iguaçu basin. Neotropical Ichthyology, 10: 263-283.; Zawadzki ., 2013Zawadzki, C. H. , R. R. de Oliveira & T. Debona. 2013. A new species of Hypostomus Lacépède, 1803 (Siluriformes: Loricariidae) from the rio Tocantins-Araguaia basin, Brazil. Neotropical Ichthyology, 11: 73-80.). There are 11 nominal valid species described from the rio Paraguai basin: H. cochliodon (Kner), H. ternetzi (Boulenger), H. borellii (Boulenger), H. boulengeri (Eigenmann & Kennedy), H. latirostris (Regan), H. variostictus (Miranda Ribeiro), H. latifrons Weber, H. piratatu Weber, H. mutucae Knaack, H. peckoltoides Zawadzki, Weber & Pavanelli, and H. careopinnatus Martins, Marinho, Langeani & Serra. In addition, H. regani (Ihering), originally described from the upper rio Paraná basin also occurs in the upper rio Paraguai basin (Weber ., 1992Weber, C. , S. Muller & V. Mahnert. 1992. Harnischwelse Paraguays. DATZ (Sonderheft Harnischwelse): 10-13.; Veríssimo ., 2005Veríssimo, S. , C. S. Pavanelli, H. A. Britski & M. M. M. Moreira. 2005. Fish, Manso Reservoir region of influence, Rio Paraguai basin, Mato Grosso State, Brazil. Check List, 1: 1-9.; Zawadzki, Renesto, Peres & Paiva, 2008).

The Bodoquena region is drained by the Apa, Formoso, Formosinho, Perdido, Miranda, rio do Peixe, Salobra, and Sucuri rivers, all part of the rio Paraguai basin (Boggiani, 1999Boggiani, P. C. 1999. Por que Bonito é Bonito? - Geologia da Serra da Bodoquena. Pp. 10-23. In: Scremin-Dias, E., V. J. Pott, R. C. Hora & P. R. Souza (Eds.). Nos Jardins Suspensos da Bodoquena - Guia para Identificação de Plantas Aquáticas de Bonito e Região. Campo Grande, Editora da UFMS.; Salles ., 2006Salles, L. O. , C. Cartelle, P. G. Guedes, P. C. Boggiani, A. Janoo & C. A. M. Russo. 2006. Quaternary mammals from Serra da Bodoquena, Mato Grosso do Sul, Brazil. Boletim do MuseuNacional, 521: 1-12.). According to Boggiani (1999) some of those rivers flow through calcareous terrain resulting in a low turbidity and very clear waters. The region is known for its large aquatic biodiversity and endemism (Scremin-Dias ., 1999Scremin-Dias, E. , V. J. Pott, R. C. Hora & P. R. Souza. 1999. Nos jardins submersos da Bodoquena: guia de identificação de plantas aquáticas de Bonito e região. Campo Grande, Editora da UFMS.). Sabino & Trajano (1997)Sabino, J. & E. Trajano. 1997. A new species of blind armoured catfish, genus Ancistrus, from caves of Bodoquena region, Mato Grosso do Sul, southwestern Brazil. Revue Française d'Aquariologie, 24: 73-78. described Ancistrus formoso, an albino cave dwelling armored catfish and, then, ten years later Ribeiro . (2007)Ribeiro, A. C. , M. R. Cavallaro & O. Froehlich. 2007. Oligosarcus perdido (Characiformes, Characidae), a new species of freshwater fish from Serra da Bodoquena, upper Rio Paraguai basin, Brazil. Zootaxa, 1560: 43-53. published the discovery of a new characin Oligosarcus perdido from that region.

Examination of specimens of the genus Hypostomus from the rio Perdido, a tributary to rio Apa of the rio Paraguai basin, revealed a population with an unusual pattern of unicuspid teeth. The aim of this paper is to establish it as a new species of Hypostomus from the Bodoquena Plateau.

Material and Methods

Measurements were made with digital calipers to the nearest 0.1 mm. Methodology and terminology for measurements follow Boeseman (1968)Boeseman, M. 1968. The genus Hypostomus Lacépède, 1803, and its Surinam representatives (Siluriformes, Loricariidae). Zoologische Verhandelingen, 99: 1-89. with modifications by Weber (1985)Weber, C. 1985. Hypostomus dlouhyi, nouvelle espèce de poisson-chat cuirassé du Paraguay (Pisces, Siluriformes, Loricariidae). Revue suisse de Zoologie, 92: 955-968. and Zawadzki (2008)Zawadzki, C. H. , E. Renesto, M. D. Peres & S. Paiva. 2008. Allozyme variation among three populations of the armored catfish Hypostomus regani (Ihering, 1905) (Siluriformes: Loricariidae) from the Paraná and Paraguay river basins, Brazil. Genetics and Molecular Biology, 31: 767-771.. Plate counts and nomenclature follow Schaefer (1997)Schaefer, S. A. 1997. The Neotropical cascudinhos: systematics and biogeography of the Otocinclus catfishes (Silurifiormes: Loricariidae). Proceedings of the Academy of Natural Sciences of Philadelphia, 148: 1-120., with the modifications of Oyakawa . (2005)Oyakawa, O. T. , A. Akama & A.M. Zanata. 2005. Review of the genus Hypostomus Lacépède, 1803 from Rio Ribeira de Iguape basin, with description of a new species (Pisces, Siluriformes, Loricariidae). Zootaxa, 921: 1-27.. Vertebral counts were taken on cleared-and-stained (c&s) specimens, according to Taylor & Van Dyke (1985)Taylor, W. R. & G. C. Van Dyke. 1985. Revised procedures for staining and clearing small fishes and other vertebrates for bone and cartilage study. Cybium, 9: 107-119. procedures. The vertebral complex of the Weberian apparatus and the compound caudal centrum were counted as a single element (Lundberg & Baskin, 1969Lundberg, J. G. & J. N. Baskin. 1969. The caudal skeleton of the catfishes. Order Siluriformes. American Museum Novitates, 2398: 1-49.). Osteological nomenclature follows Schaefer (1987)Schaefer, S. A. 1987. Osteology of Hypostomus plecostomus (Linnaeus), with a phylogenetic analysis of the loricariid subfamilies (Pisces: Siluroidei). Contributions in Science, 394: 1-31.. Standard length (SL) is expressed in millimeters; some measures are expressed as percents of SL; some as percents of head length (HL) and additionally, some other percents are according to Zawadzki (2010)Zawadzki, C. H. , C. Weber & C. S. Pavanelli. 2010. A new dark-saddled species of Hypostomus (Siluriformes: Loricariidae) from the upper rio Paraguay basin. Neotropical Ichthyology, 8: 719-725.. Meristic and morphometric ranges of the type series of Hypostomus fonchii Weber & Montoya-Burgos cited in the diagnosis section of the present work are from Weber & Montoya-Burgos (2002)Weber, C. & J. I. Montoya-Burgos. 2002. Hypostomus fonchii sp. n. (Siluriformes: Loricariidae) from Peru, a key species suggesting the synonymy of Cochliodon with Hypostomus. Revue suisse de Zoologie, 109: 355-368.. In Table 1, range is composed by the minimum and maximum values of the holotype, plus 19 paratypes. Institutional abbreviations are: ANSP, Academy of Natural Sciences of Drexel University, Philadelphia; BMNH, Natural History Museum, London; CPUFMT, Coleção de Peixes da Universidade Federal do Mato Grosso, Cuiabá; INPA, Instituto Nacional de Pesquisas da Amazônia, Manaus; MCP, Museu de Ciências e Tecnologia, Pontifícia Universidade Católica do Rio Grande do Sul, Porto Alegre; MHNG, Museum d'histoire naturelle, Geneva; MNHN, Muséum National d'histoire naturelle, Paris; MNRJ, Museu Nacional, Universidade Federal do Rio de Janeiro, Rio de Janeiro; MZUSP, Museu de Zoologia, Universidade de São Paulo, São Paulo; NUP, Coleção Ictiológica do Núcleo de Pesquisas em Limnologia, Ictiologia e Aquicultura da Universidade Estadual de Maringá, Maringá; RMNH, Naturalis Biodiversity Center, Leiden; UMSS, Universidad Mayor de San Simón, Cochabamba; ZSM, Zoologische Staatssammlung München, Munich; ZUEC, Museu de Zoologia da Universidade Estadual de Campinas "Adão José Cardoso", Campinas; ZUFMS-PIS, Coleção Zoológica de Referência da Universidade Federal de Mato Grosso do Sul, Campo Grande.

Table 1
Morphometric data and counts of Hypostomus perdido. SD = standard deviation; N = holotype plus 19 specimens.

Results

Hypostomus perdido, new species

Figs. 1-2a,c

Fig. 1
Hypostomus perdido, holotype, MZUSP 111064, 159.1 mm SL, Brazil, Mato Grosso do Sul State, Bodoquena, rio Paraguai basin, rio Perdido. Dorsal (top), lateral (middle), and ventral (bottom) views.

Fig. 2
Mouth and right dentary close up of Hypostomus perdido, paratype, CPUFMT 1500, 170.3 mm SL (a and c) and of Hypostomus fonchii UMSS 00360, 154.0 mm SL (b and d), respectively.

Hypostomus sp. 2-Rio Perdido NUP 4249: Cereali ., 2008Cereali, S. S. , E. Pomini, R. Rosa, C. H. Zawadzki, O. Froehlich & L. Giuliano-Caetano. 2008. Karyotype description of two species of Hypostomus (Siluriformes, Loricariidae) of the Planalto da Bodoquena, Brazil. Genetics and Molecular Research, 7: 583-591.: 587 (cytogenetic data, karyotype).

Holotype. MZUSP 111064, 159.1 mm SL, Brazil, Mato Grosso do Sul, Bodoquena, rio Paraguai basin, rio Perdido, 21°17'09"S 56°41'47"W, 8 Sep 2005, O. Froehlich.

Paratypes. All collected with the holotype (61 specimens). ANSP 193370, 2, 163.6-171.3 mm SL. CPUFMT 1500, 2, 152.5-170.3 mm SL. INPA 37689, 1, 144.4 mm SL. MCP 47141, 2, 133.9-147.9 mm SL. MNRJ 40094, 2, 126.0-153.1 mm SL. NUP 12143, 10, 136.4-166.3 mm SL. NUP 12144, 18, 109.1-152.4 mm SL. NUP 14406, 1 c&s, 124.0 mm SL. ZSM 41828, 1, 149.5 mm SL. ZUEC 7254, 2, 140.2-141.7 mm SL. ZUFMS-PIS 1468, 20, 126.6-181.0 mm SL.

Diagnosis.Hypostomus perdido is distinguished from all congeners, except H. fonchii, by having unicuspid teeth (vs. bicuspid teeth). From H. fonchii it is distinguished by having fewer dermal plates in the median series of lateral plates (26-27 vs. 28), fewer premaxillary teeth (7-10 vs. 18-21), fewer dentary teeth (8-13 vs. 18-25), a more depressed head (head depth 15.8-18.1% in SL vs. 19.1-22.0%), and by the presence of median buccal papilla (vs. its absence).

Description. Measurements and counts in Table 1. Dorsal profile of head convex from tip of snout to supraoccipital posterior end; straight from that point to dorsal-fin origin. Head elevated and compressed. Snout narrow and compressed, covered by irregular series of several small plates. Mesethmoid forming conspicuous bulge from snout tip to nares. Upper orbital margin not elevated. Eye laterodorsally positioned. Interorbital region wide and flat in frontal view. Very slender keel on upper portion of pterotic-supracleithrum just posterior to orbit. Opercle considerably large and somewhat ellipsoidal; its horizontal length similar to orbital diameter; odontodes slightly larger on posterior margin. Predorsal region almost flat; usually with one single larger plate surrounding supraoccipital followed by two narrow plates in front of dorsal-fin spinelet. Dorsal profile of trunk tapering straight from dorsal-fin insertion to caudal peduncle posterior portion; ascending to caudal fin. Adipose fin long, almost same length of minimum caudal peduncle depth. Maximum body width at region of dorsal-fin origin; profile gradually tapering from this point to caudal fin. Caudal peduncle somewhat ellipsoid in cross-section; dorsal and ventral caudal peduncle region slightly flattened.

Dorsal fin II,7; distal margin slightly convex to straight; origin at vertical two plates before pelvic-fin insertion; adpressed rays not reaching adipose-fin spine. Pectoral fin I,6; distal margin straight and almost reaching from one-third to half pelvic-fin length, odontodes more developed on distal dorsal region. Pelvic fin I,5; distal margin straight to slightly convex; distal portion of unbranched pelvic-fin ray reaching or slightly surpassing anal-fin insertion when adpressed to body. Anal fin I,5; distal border rounded. Caudal fin I,14,I, posterior margin truncate to slight emarginated; lower lobe slightly longer than upper lobe. Vertebrae 27; ribs 9, first rib relatively larger than others.

Dorsal and lateral surface of head and body covered with dermal plates, except snout tip and area surrounding dorsal-fin base. Plates on lateral margin of head, from snout tip to pterotic-supracleithrum small and irregular. Five lateral series of plates on trunk. Dorsal, mid-dorsal, median, mid-ventral and ventral series without keels. Lateral line complete on median lateral series. Mid-ventral series moderately bent on anterior portion. Ventral region of body with small platelets bearing odontodes, except area beneath lower lip, insertion of pectoral and pelvic fins, and anterior region of anus. Naked areas reduced on larger specimens. Lips round; covered with dense papillae, which decrease in size to distal border. Median buccal papilla sensu Armbruster (2003Armbruster, J. W. 2003. The species of the Hypostomus cochliodon group (Siluriformes: Loricariidae). Zootaxa, 249: 1-60., Fig. 03) present. Buccal skin internally bordering premaxilla and dentary with unorganized series of flat enlarged papillae (Fig. 02a,c). Maxillary barbel elongate and proximately joined to labial border by membrane; distal tip free. Premaxilla with 7 to 10 teeth, dentary 8 to 13 teeth; teeth robust, moderate in length, unicuspid, crown short and continuous to stalk (without notch between stalk and crown). Dentary rami straight and angled 82 to 94° from each other (n = 20 specimens; mean = 85.8°).

Fig. 3
Distribution of Hypostomus perdido. Red star symbol represents its type locality, the rio Perdido, rio Paraguai basin, Mato Grosso do Sul State, Brazil. Inset in the right upper corner highlights the area into a South American perspective.

Color in alcohol. Dorsal ground color of body and fins grayish brown. Trunk and fins densely covered by faint darker spots; spots smaller on head and larger on fins and posterior portions of body. All spines and unbranched-fin rays with spots. Dorsal, pectoral, and pelvic fins with one series of spots on each interradial membrane. Dorsal-fin spots usually larger than spots in remaining fins and usually aligned to form five to seven horizontal bands; spots mottled in some specimens. Anal-fin spots more faded than remaining fin spots. Abdominal region pale yellowish. Ventral surface of body and paired fins spotless.

Distribution. The new species is known from its type locality, the rio Perdido, tributary to the rio Apa, rio Paraguai basin, Mato Grosso do Sul State, Brazil (Fig. 03).

Ecological notes.The upper 50 km of the rio Perdido flows from elevations of 550 m to 350 m through the calcareous Bodoquena Plateau. It initially flows to the southeast, passes about 2 to 3 km as subterranean portion, then turns roughly southwards and bisects the Parque Nacional da Serra da Bodoquena, where the river flows confined in open folds of the Paraguai Fold Belt. Then the river turns to the southwest, descends the plateau escarpments and flows 250 km further before discharging in the rio Apa, at roughly 100 m altitude. In the plateau, the river is 10 to 12 m wide and is dammed by several calcareous tufa deposits, some of them forming waterfalls from one to five meters high. The dammed sections can be as deep as 12 m, with vertical rock banks and very slow flow; the substrate is a whitish calcareous clay on which lay many submerged logs, branches and even whole trees. The water is very clear throughout the dry season. However, transparency is significantly reduced in the rainy season, mainly due to suspended clay. Specimens of Hypostomus perdido were collected in stretches of sluggish to still waters.

Etymology. The specific name perdido alludes to the type locality rio Perdido. From the Portuguese "perdido", which means lost. An adjective nominative, masculine, and singular.

Discussion

The unusual teeth morphology of Hypostomus perdido distinguishes the new species not only from its congeners from the rio Paraguai basin, but from nearly all species of the genus. The only exception is H. fonchii, described from the west tributaries to the middle río Ucayali in Peru, which also has unicuspid teeth (Fig. 02b and 2d). Hypostomus fonchii (Fig. 04) also inhabits Bolivian streams flowing to the rio Mamoré. Despite the tooth similarity, H. perdido is more depressed than H. fonchii, has less dermal plates on the median series and less teeth on premaxilla and on dentary. Weber & Montoya-Burgos (2002)Weber, C. & J. I. Montoya-Burgos. 2002. Hypostomus fonchii sp. n. (Siluriformes: Loricariidae) from Peru, a key species suggesting the synonymy of Cochliodon with Hypostomus. Revue suisse de Zoologie, 109: 355-368. addressed H. fonchii to the H. cochliodon group due to its unicuspid tooth pattern. Armbruster (2003)Armbruster, J. W. 2003. The species of the Hypostomus cochliodon group (Siluriformes: Loricariidae). Zootaxa, 249: 1-60. noted that the species of H. cochliodon group did not possess unicuspid teeth but bicuspid teeth with lateral cusp usually fused to mesial cusp and rejected a close relationship with H. fonchii because the body morphology did not agree with the typical body shape of the members of the H. cochliodon group. Armbruster (2003)Armbruster, J. W. 2003. The species of the Hypostomus cochliodon group (Siluriformes: Loricariidae). Zootaxa, 249: 1-60. also commented that specimens of H. fonchii were not examined by him, in that work. Herein, we verified the tooth morphology of H. fonchii finding clearly unicuspid teeth, but it is anyway much slender than the teeth of H. perdido.

Fig. 4
Lateral view of Hypostomus fonchii, UMSS 00360, 154.0 mm SL, río Chipiriri, río Mamoré basin, Bolivia.

Montoya-Burgos . (2002)Montoya-Burgos, J. I. , C. Weber & P-Y. Le Bail. 2002. Phylogenetic relationship within Hypostomus (Siluriformes: Loricariidae) and related genera based on mitochondrial D-loop sequences. Revue suisse de Zoologie, 109: 369-382.performed a phylogenetic analysis based on mitochondrial D-loop sequences data and recovered Hypostomus fonchii within the H. cochliodongroup of species, corroborating the initial proposition of Weber & Montoya-Burgos (2002)Weber, C. & J. I. Montoya-Burgos. 2002. Hypostomus fonchii sp. n. (Siluriformes: Loricariidae) from Peru, a key species suggesting the synonymy of Cochliodon with Hypostomus. Revue suisse de Zoologie, 109: 355-368.. The position of H. fonchii within the H. cochliodon group of species was also maintained in Montoya-Burgos (2003)Montoya-Burgos, J. I. 2003. Historical biogeography of the catfish genus Hypostomus (Siluriformes: Loricariidae), with implications on the diversification of Neotropical ichthyofauna. Molecular Ecology, 12: 1855-1867.. Therefore, we consider H. fonchii somewhat morphologically compatible with the H. cochliodon group species. Contrary to H. fonchii, H. perdido indeed does not resemble representatives of the H. cochliodon group of species, since it possesses slender body (vs. robust) and rounded snout (vs. triangular). In addition, the new species presents dentary rami angled to each other from 82 to 94° versus less than 80° in the species of the H. cochliodon group. To elucidate the phylogenetic relationships of the new species a cladistic analysis based on morphological and/or molecular data would be necessary. However, considering the aforementioned differences, it would be plausible that unicuspid teeth character had arisen independently.

Cytogenetic data are already available to Hypostomus perdido. The species was named as "Hypostomus sp 2-Rio Perdido NUP 4249" by Cereali . (2008)Cereali, S. S. , E. Pomini, R. Rosa, C. H. Zawadzki, O. Froehlich & L. Giuliano-Caetano. 2008. Karyotype description of two species of Hypostomus (Siluriformes, Loricariidae) of the Planalto da Bodoquena, Brazil. Genetics and Molecular Research, 7: 583-591.. Except H. perdido, the diploid number in Hypostomus ranges from 54 to 82 (Bueno ., 2012Bueno, V. S. , P. C. Venere, C. H. Zawadzki & V. P. Margarido. 2013. Karyotype diversification in Hypostomus Lacépède, 1803 (Osteichthyes, Loricariidae): biogeographical and phylogenetic perspectives. Reviews in Fish Biology and Fisheries, 23: 103-112.). Cereali . (2008)Cereali, S. S. , E. Pomini, R. Rosa, C. H. Zawadzki, O. Froehlich & L. Giuliano-Caetano. 2008. Karyotype description of two species of Hypostomus (Siluriformes, Loricariidae) of the Planalto da Bodoquena, Brazil. Genetics and Molecular Research, 7: 583-591. found H. perdido with 84 chromosomes (2n = 84), as the greatest diploid number known in Hypostomus (Martinez ., 2011Martinez, E. R. M. , C. H. Zawadzki, F. Foresti & C. Oliveira. 2011. Cytogenetic analysis of five Hypostomus species (Siluriformes, Loricariidae). Genetics and Molecular Biology, 34: 562-568.; Rubert ., 2011Rubert, M. , R. da Rosa, F. C. Jerep, L. A. C. Bertollo & L. Giuliano-Caetano. 2011. Cytogenetic characterization of four species of the genus Hypostomus Lacépède, 1803 (Siluriformes, Loricariidae) with comments on its chromosomal diversity. Comparative Cytogenetics, 5: 397-410.; Endo ., 2012Endo, K. S. , E. R. M. Martinez, C. H. Zawadzki, L. R. S. Paiva & H. F. JúlioJr. 2012. Karyotype description of possible new species of the Hypostomus ancistroides complex (Teleostei: Loricariidae) and other Hypostominae. Acta Scientiarum. Biological Sciences, 34: 181-189.; Bueno ., 2013Bueno, V. S. , C. H. Zawadzki & V. P. Margarido. 2012. Trends in chromosome evolution in the genus Hypostomus Lacépède, 1803 (Osteichthyes, Loricariidae): a new perspective about the correlation between diploid number and chromosomes types. Reviews in Fish Biology and Fisheries, 22: 241-250.).

Comparative material. Hypostomus ancistroides . Brazil. São Paulo State. Rio Paraná basin. MZUSP 2131, 4, 95.6-165.1 mm SL, rio Tatuí. Hypostomus borellii. Bolivia. Rio Paraguai basin. BMNH 1897.1.27.19, 1, 153.1 mm SL, syntype, río Pilcomayo. Hypostomus boulengeri. Brazil. Mato Grosso State. Rio Paraguai basin. NUP 414, 3, 165.8-175.6 mm SL; NUP 3273, 8, 110.0-166.0 mm SL; NUP 8695, 1, 170.0 mm SL, rio Manso. NUP 1078, 2, 210.0-220.0 mm SL, rio Manso Reservoir. NUP 8692, 1, 190.0 mm SL, rio Quilombo. Hypostomus careopinnatus. Brazil. Mato Grosso State. Rio Paraguai basin. NUP 11257, 5, 30.2-53.8 mm SL, paratypes, tributary of rio Ariranha. Hypostomus cochliodon. Brazil. Mato Grosso State. Rio Paraguai basin. NUP 2274, 2, 42.2-200.4 mm SL; NUP 3602, 1, 153.8 mm SL; NUP 2274, 2, 42.2-200.4 mm SL, rio Manso. Hypostomus commersoni. Uruguay. Montevideo Department. Río de La Plata basin. MNHN A.9444, 1, 425.00 mm SL, holotype, río de la Plata. Hypostomus dlouhyi. Paraguay. Alto Paraná Department. Río Paraná basin. MHNG 2229.43, 1, 139.5 mm SL, holotype, río Yguazú. Hypostomus fonchii. Bolivia. Río Mamoré basin. UMSS 00360, 1, 154.0 mm SL, río Chipiriri. Peru. San Martin Department. Río Ucayali basin. MHNG 2613.066, 141.0 mm SL, holotype, Quebrada John, near mouth of río Pauya. Hypostomus laplatae. Argentina. Río de La Plata basin. BMNH 1908.8.29.17, 1, 207.3 mm SL, río de La Plata. Hypostomus latifrons. Brazil. Mato Grosso State. Rio Paraguai basin. NUP 1039, 3, 240.0-260.0 mm SL, rio Manso Reservoir. NUP 3405, 1, 270.0 mm SL, Sinhá Mariana bay. Paraguay. Presidente Hayes Department. Río Paraguai basin. MHNG 2256.67, 228.2 mm SL, holotype, río Araguay-guazú. Hypostomus latirostris. Brazil. Mato Grosso State. Rio Paraguai basin. BMNH 1892.4.20.26-27, 2, 137.2-159.3 mm SL, syntypes, rio Jangada. NUP 12203, 1, 113.0 mm SL, rio Casca. NUP 12204, 1, 55.0 mm SL, rio Manso. NUP 12205, 2, 75.0-120.0 mm SL, rio Cuiabá; NUP 12206, 1, 104.0 mm SL, rio Palmeiras; NUP 12323, 1, 109.0 mm SL, rio Cuiabazinho. Hypostomus microstomus. Paraguay. Itapua Department. Rio Paraná basin. MHNG 2367.90, 197.5 mm SL, holotype, río Paraná. Hypostomus mutucae. Brazil. Mato Grosso State. Rio Paraguai basin. MCP 28669, 67.7 mm SL, holotype, rio Mutuca. NUP 6641, 13, 52.4-109.2 mm SL; NUP 6642, 4, 62.1-98.1 mm SL, rio Claro. Hypostomus nigromaculatus. Brazil. São Paulo State. Rio Paraná basin. MZUSP 22674, 9, 43.8-75.9 mm SL, cachoeira de Emas, rio Mogi-Guaçu. Hypostomus paranensis. Argentina. Cordoba Department. Río Paraná basin. BMNH 1878.4.4.1, 178.3 mm SL, holotype of Plecostomus cordovae, río Paraná. MZUSP 23805, 6, 47.5-111.3 mm SL, río Segundo, Pilar, río Paraguay basin. Hypostomus peckoltoides. Brazil. Mato Grosso State. Rio Paraguai basin. NUP 5216, 2, 88.9-92.8 mm SL; NUP 5217, 3, 85.5-98.2 mm SL; MZUSP 105226, 110.7 mm SL, holotype, rio Cuiabá. Hypostomus piratatu. Paraguay. Paraguarí Department. Río Paraguay basin. MHNG 2265.03, 214.0 mm SL, holotype, río Paraguai. Hypostomus plecostomus. Suriname. RMNH 18240, 1, 121.4 mm SL, Suriname Rivier. Hypostomus regani. Brazil. Mato Grosso State. Rio Paraguai basin. NUP 1032, 3, 260.0-270.0 mm SL, Manso Reservoir. NUP 7917, 3, 92.0-107.0 mm SL, rio Ariranha. NUP 8325, 1, 130.0 mm SL, córrego Roncador. Mato Grosso do Sul State. Rio Paraguai basin. NUP 9820, 2, 129.5-37.7 mm SL, córrego da Onça. São Paulo State. Rio Paraná basin. BMNH 1905.6.7.3, 174.2 mm SL, holotype, rio Piracicaba. Hypostomus ternetzi. Brazil. Mato Grosso State. Rio Paraguai basin. BMNH 1895.5.17.64, 210.2 mm SL, holotype, rio Paraguai.

Acknowledgments

We are grateful to Fernando Jerep (MZUEL), Héctor Vera-Alcaraz, and Richard Kleinhardt for their comments and suggestions for the manuscript; to Marcel Cavallaro, Ismael Escote and Emanuele Pomini for helping during scuba observations; to Maria José Vilela, Renata Vargas, Ottilie Forster and Nereida de Almeida for help during collecting trips. Thanks are also due to Mark Sabaj-Pérez (ANSP), Patrick Campbell (BMNH), Carlos Lucena and Margarete Lucena (MCP), Claude Weber and Sonia Fisch-Muller (MHNG), Patrice Pruvost (MNHN), Paulo Buckup and Marcelo Britto (MNRJ), Osvaldo Oyakawa (MZUSP), Dirk Neumann (ZSM) and Fernando Carvajal (UMSS) for loan of comparative material and hosting museum visits. Nupélia provided us with logistical support. Visits to museum collections by CHZ were funded by the All Catfish Species Inventory (DEB-0315963). CAPES (Coordenação de Aperfeiçoamento de Pessoal de Nível Superior) provided grants to LFCT. CNPq (Conselho Nacional de Desenvolvimento Científico e Tecnológico) provided a grant to CHZ (Proc. 310733/2013-8).

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Publication Dates

  • Publication in this collection
    Jan-Mar 2014

History

  • Received
    12 Aug 2012
  • Accepted
    27 Nov 2013
Sociedade Brasileira de Ictiologia Universidade Estadual de Maringá, Núcleo de Pesquisas em Limnologia, Ictiologia e Aquicultura/Coleção Ictiologia, Av. Colombo, 5790, 87020-900 Maringá, PR, Brasil, Tel.: (55 44)3011 4632 - Maringá - PR - Brazil
E-mail: neoichth@nupelia.uem.br