Parotocinclus seridoensis, Ramos & Barros-Neto & Britski & Lima, 2013

Ramos, Telton Pedro A., Barros-Neto, Luciano F., Britski, Heraldo A. & Lima, Sergio M. Q., 2013, Parotocinclus seridoensis, a new hypoptopomatine catfish (Siluriformes: Loricariidae) from the upper rio Piranhas-Açu basin, northeastern Brazil, Neotropical Ichthyology 11 (4), pp. 787-796 : 788-793

publication ID

https://doi.org/ 10.1590/S1679-62252013000400006

persistent identifier

https://treatment.plazi.org/id/262087AB-8B2E-FFED-FF58-F997FA71EC7D

treatment provided by

Felipe

scientific name

Parotocinclus seridoensis
status

sp. nov.

Parotocinclus seridoensis View in CoL , new species Fig. 1 View Fig

Holotype. MZUSP 113422 View Materials , 37.7 mm SL (Female); Brazil, Rio Grande do Norte State, Caicó Municipality, rio Seridó, rio Piranhas-Açu basin, 6°27’28.4”S 37°05’10.7”W, 11 Jun 2012, S. Lima, W. Berbel, L. Neto, C. Neves, C. Alencar, D. Ferreira & F. Landim. GoogleMaps

Paratypes. All from Brazil, rio Piranhas-Açu basin . Rio Grande do Norte. MZUSP 113423 View Materials , 3 View Materials , 33.6-41.8 mm SL ; MNRJ 40715 View Materials , 1 View Materials , 31.6 mm SL ; UFRN 240 , 1 , 30.6 mm SL; same data as holotype GoogleMaps . MNRJ 40716 View Materials , 5 View Materials , 26.1-35.2 mm SL ; MZUSP 113424 View Materials , 6 View Materials , 26.9-36.9 mm SL ; UFPB 9218 View Materials , 5 View Materials , 28.1 View Materials - 39.7 View Materials ; UFRN 005 , 4 , 29.8 -37.0 mm SL (2 c&s); same locality as holotype, 04 May 2011, P. Medeiros & J. Medeiros GoogleMaps . UFRN 303 , 1 , 34.2 mm SL, Jardim de Piranhas Municipality, rio Piranhas , 6°22’40.3”S 37°21’19.3”W, 13 Jun 2012, S. Lima, W. Berbel, L. Neto, C. Neves, C. Alencar, D. Ferreira & F. Landim GoogleMaps . Paraíba. UFRN 1588 , 1 , 32.18 mm SL, Pombal Municipality, rio Piranhas , 6°43’12.1”S 37°47’11.6”W, 13 Apr 2013, M. Silva GoogleMaps ; MCP 31463 View Materials , 19 View Materials , 24.0- 34.5 mm SL (2c&s), rio Piranhas in BR-230 between Pombal and Souza , 5 Km of Pombal , 6°43’31.9”S 37°47’49.9”W, 20 Nov 2002, C. Lucena, E. Pereira & J. Pezzi GoogleMaps . UFRN 1590 , 1 c&s, 35.4 mm SL, Ibiara Municipality, rio Piancó , 7º28’33.7”S 38º21’10.3”W, 24 Apr 2013, T. Ramos, L. Neto, R. Paiva & M. Germano GoogleMaps .

Diagnosis. The new species differs from all its congeners, except Parotocinclus bidentatus Gauger & Buckup , P.muriaensis Gauger & Buckup and P. spilurus (Fowler) by presenting adipose fin rudimentary or absent. Parotocinclus seridoensis differs from P. bidentatus , P. muriaensis and P. spilurus by presenting abdomen almost naked, with a single row of elongate reduced plates on each side and a group of small rounded plates irregularly distributed on preanal region (vs. abdomen completely covered of dermal plates between the pectoral girdle and the anus), and also by presenting bright spots, usually about as large as the eye diameter or larger on sides of the body predominantly disposed in two rows (dorsally and ventrally) (vs. body without spots in P. bidentatus and P. muriaensis ; and with numerous small bright spots about as large as pupil diameter scattered on body and head in P. spilurus ). Parotocinclus seridoensis also differs from P. bidentatus and P. muriaensis , but not to P. spilurus by the presence of of pectoral girdle medially covered by skin and laterally exposed, supporting odontodes only laterally (vs. completely exposed). It also differs from P. spilurus by the presence of an area deprived of odontodes at the anterior border of the snout shaped as an inverted V or U (vs. anterior border of the snout covered by regular rows of odontodes).

In addition to the adipose fin rudimentary or vestigial Parotocinclus seridoensis is further distinguished from congeners of northeastern Brazil, except P. arandai , P. cearensis , P. cesarpintoi , P. jumbo , P. minutus , and P. spilosoma , by having abdomen nearly naked, with only one or two row of plates on each side and median row of platelets irregularly distributed (vs. abdomen entirely covered by larges plates between the pectoral girdle and preanal region in P. cristatus , P. jimi , and P. haroldoi , and abdomen completely naked with only preanal platelets in P. bahiensis ). Parotocinclus seridoensis also shares with P. bahiensis , P. cearensis , and P. jumbo the pectoral girdle covered by skin medially and laterally exposed, and supporting odontodes only laterally (vs. scapular bridge completely exposed in P. arandai , P. cesarpintoi , P. cristatus , P. jimi , P. haroldoi , P. minutus , and P. spilosoma ).

Description. Morphometric and meristic data of holotype and paratypes are presented in Table 1 and 2. Body up to 42.6 mm SL. Body moderately short and somewhat depressed. Greatest body width at cleithrum, progressively tapering to end of caudal peduncle. Dorsal profile slightly convex from snout to parieto-supraoccipital tip; straight between parieto-supraoccipital and dorsal fin origin; descendent at dorsal-fin base; slightly concave from dorsal-fin end to rudimentary adipose fin (or azygous plate indicating its position); straight or slightly concave from this point to base of uppermost caudal-fin rays. Ventral body profile of head straight or slightly concave; ventral profile of trunk somewhat straight from pectoral girdle to posterior base of pelvic fin; somewhat concave at anus region, straight at anal-fin base and straight from anal-fin end to lowermost caudal-fin rays. Head depressed and round in dorsal view. Eyes moderately small, positioned midway between snout tip and pterotic-supracleithrum posterior margin; distance between orbit margin and ventral surface of head greater than orbital diameter. Dorsal iris diverticulum present. Interorbital space straight or slightly convex. Pectoral girdle exposed only laterally; median region covered by skin ( Fig. 3 View Fig ); coracoids laterally covered by odontodes; arrector fossae ellipsoid, small, extending laterally, almost meeting in at midline ( Fig. 4 View Fig ). Snout rounded in dorsal view. Greatest body depth at dorsal-fin origin. Individuals with two depressions on snout; inferior rostral margin of snout with posteriorly directed odontodes similar in size to those on dorsal portion of snout, sometimes with an area variable in extension deprived of odontodes at the anteroventral border of snout shaped as an inverted V or U. Odontodes on upper part of head, roughly arranged in rows. Mouth small. Oral disk approximately round, papillose; maxillary barbels slightly shorter than orbital diameter. All teeth slender and bifid. Accessory patch of uniscupid teeth absent. Head depressed and round in dorsal view. Eye moderately small and dorsolaterally positioned; distance between ventral margin of orbit and ventral surface of head greater than orbital diameter. Trunk depressed on insertion of dorsal and anal fin. Caudal peduncle rounded in cross section.

Dorsal fin i,7; its origin slightly posterior to pelvic-fin origin; dorsal fin when adpressed extending to vertical through beyond anal-fin base. Pectoral fin i,6; pectoral spine reaching one quarter to one third of length of unbranched pelvic-fin ray. Pelvic-fin rays i,5; unbranched ray curved, covered with small odontodes; pelvic fin reaching beyond anus, ending just anterior to anal-fin origin. Anal-fin rays i,5; origin of anal fin covering three plates. Caudal fin slightly notched, emarginate, with lower lobe slightly pointed and longer upper lobe; principal caudal-fin rays i,14,i. Lateral-line canal in median series complete, pore tube visible from pterotic-supracleithrum to caudal peduncle. Abdomen nearly naked; with only one or two row of small plates elongate and rounded on each side arranged near the pectoral girdle, and a group of small rounded plates irregularly distributed on preanal region ( Fig. 3 View Fig ); some young individuals with two or three platelets in the middle of abdomen. Dorsal-fin spine flexible, followed by seven branched rays. Dorsal-fin locking mechanism nonfunctional. Nuchal plate exposed, not covered by skin. Dorsal-fin spinelet present, V-shaped, wider than base of dorsal spine.Adipose fin rudimentary or vestigial. Total vertebrae 24 (2 c&s).

Coloration. Ground color in ethanol dark gray to dark brown. Dorsal and lateral portions of head uniform in color with a bright spot on pineal region; ventral area of head yellowish. Trunk with clear spots, usually uniform in size, diameter, form (usually rounded) and distribution, forming sometimes two alternate longitudinal series, dorsally and ventrally, extending from gill opening to caudal peduncle, ending in two conspicuous whitish yellow blotches vertically arranged. Abdomen yellowish white, anterior region (pectoral girdle to anus) with little dark chromatophores, posterior region with conspicuous dark chromatophores. Dorsal and caudal-fin rays with dark chromatophores, forming irregular set of stripes that alternates between dark gray and brownish yellow: three on dorsal fin and four on caudal fin; tip of caudal-fin lobes intensively pigmented with dark chromatophores. Pectoral, pelvic- and anal-fin rays with few and sparse chromatophores forming a set of inconspicuous stripes. Live coloration ( Fig. 2 View Fig ) with same pattern described above, only becoming clearer in fixed specimens.

Sexual dimorphism. Males possess urogenital papilla positioned just behind the anal opening and a low fleshy flap along the dorsal margin of the first pelvic-fin ray, that is absent in females.

Distribution. Parotocinclus seridoensis is only known from four localities in the upper rio Piranhas-Açu basin, which is formed by two main tributaries, the rio Piranhas itself in the west, and the rio Seridó in the east, in the boundaries of Rio Grande do Norte and Paraíba States. Individuals of the new species were mainly found in rio Seridó, in Caicó Municipality, and in rio Piranhas main channel at Pombal Municipality, while a single specimen was caught in rio Piranhas, Jardim de Piranhas Municipality, upstream the confluence with the rio Seridó, and another in the rio Piancó, Ibiara Municipality, the southernmost record of the species, suggesting a restricted geographic distribution ( Fig. 5 View Fig ).

Etymology. The species epithet seridoensis refers the semi-arid Caatinga region, popularly known as “Sertão do Seridó”, which encompasses the upper rio Piranhas-Açu basin region in Rio Grande do Norte and Paraíba States, one of the most arid regions in northeastern Brazil, with mean annual rainfall of about 500 mm ( Silva et al., 2006). The etymology of the word “Seridó” is probably derived from the native Indian language expression “ceri-toh”. In Tapuia language it means “little foliage and little shade”, referring to the characteristic Caatinga vegetation, mainly composed by xeric shrub lands and thorn forest, that consists in small, thorny trees that shed their leaves in the dry periods.

Ecological notes. Specimens were caught in rio Seridó, type locality of the species ( Fig. 6 View Fig ), and in the rio Piranhas, both tributaries of the upper rio Piranhas-Açu basin. The “Sertão do Seridó” region is characterized by temporary rivers, due to small precipitation concentrated in few months of the year and high temperatures and evaporation ( Rosa et al., 2003). Parotocinclus seridoensis was usually found under large rocks in streams of moderate current flow and clear water ( Fig. 6 View Fig ). In these, Parotocinclus jumbo , was found in sympatry, however, inhabiting shallow and narrow streams with laminar flow, sand and gravel substrate, in the rio Seridó, while in the rio Piranhas this microhabitat was found only at the right margin, where P. jumbo was observed forming small shoals, behavior already registered by Britski & Garavello (2002).

Other species collected together with the P. seridoensis in rio Seridó were: Astyanax aff. bimaculatus , Hemigrammus marginatus Ellis , Moenkhausia sp. , Characidium bimaculatum Fowler , Hoplias malabaricus (Bloch) , Prochilodus brevis Steindachner.

Hypostomus pusarum (Starks) , Pseudancistrus papariae Fowler , Poecilia vivipara Bloch & Schneider , Cichlasoma orientale Kullander , Crenicichla menezesi Ploeg , and Oreochromis niloticus (Linnaeus) , the last one a widespread introduced species in northeastern Brazil ( Medeiros et al., 2010). In addition to these species, in rio Piranhas were also collected: Serrasalmus rhombeus (Linnaeus) , Triportheus signatus (Garman) and Trachelyopterus galeatus (Linnaeus) .

During ichthyological surveys in the upper rio Piranhas-Açu , some of the above mentioned species were only found in fast-flowing rivers, just as the rio Piranhas at Jardim de Piranhas , and the rio Seridó at Caicó, both temporary rivers made perennial by water release from Açude de Coremas and Passagem das Traíras dams, respectively. With the river disconnection by weirs and dams constructions, it is possible that these artificially perennial river stretches could represent important role in maintaining populations of rheophilic species that couldn’t reach the headwaters upstream during dry periods. Gastrointestinal contents of two specimens of P. seridoensis was mainly composed by benthic invertebrates ( Chironomidae and Coleoptera larvae) in one specimen ( UFRN 005 , 30.7 mm SL), while the other presented the tract filled with silt ( UFRN 1590 , 35.4 mm SL) .

Conservation remarks. The rio Piranhas-Açu basin is one of the largest temporary rivers of the semi-arid northeastern Brazilian area, constantly affected by drought, that will receive water from the controversial project of the artificial watershed transposition of the perennial rio São Francisco ( Lima, 2005). Although it could ensure water supply to rural and urban local people, diverting water from the rio São Francisco basin can cause many harmful environmental impacts to the aquatic biota of the river basins of the Mid-Northeastern Caatinga region, which encompasses the basins east to rio Parnaíba and north to rio São Francisco ( Rosa, 2004; Abell et al., 2008). Among these potential impacts to the aquatic organisms are: the intake of several species in the receiving basins, changes in the structure and composition of aquatic communities, species hybridization, loss of local adaptations, and local extirpation or extinction of endemic species ( Langeani et al., 2009), just as P. seridoensis .

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