Cetopsidium soniae, Vari & Ferraris Jr, 2009

Vari, Richard P. & Ferraris Jr, Carl J., 2009, New species of Cetopsidium (Siluriformes: Cetopsidae: Cetopsinae) from the upper rio Branco system in Guyana, Neotropical Ichthyology 7 (3), pp. 289-293: 290-293

publication ID

http://doi.org/ 10.1590/S1679-62252009000300001

publication LSID

lsid:zoobank.org:pub:9F613227-0523-4C89-A9C0-341AA1EBA087

persistent identifier

http://treatment.plazi.org/id/B398FEE1-4D88-4A20-8BCB-99C6BA251E0A

taxon LSID

lsid:zoobank.org:act:B398FEE1-4D88-4A20-8BCB-99C6BA251E0A

treatment provided by

Carolina

scientific name

Cetopsidium soniae
status

new species

Cetopsidium soniae   , new species Fig. 1 View Fig

Holotype. CSBD F1665; formerly MHNG 2652.014 View Materials , in part, 30.9 mm, male, Guyana, Central Rupununi (Region 9), main channel of Manari River , Takutu River basin, along road between Lethem and Annai, near Lethem, 3°26.590’N 59°44.578’W, altitude 329 m, B. Allocock, G. King, J. I. Montoya-Burgos, R. Covain, A. Fort & R. Daniels, 29 Oct 2004. GoogleMaps  

Paratype. MHNG 2652.014 View Materials , 35.9 mm, female; collected with holotype GoogleMaps   .

Diagnosis. Cetopsidium soniae   differs from its congeners in the posterior extent of the pelvic fin (falling distinctly short of the vent versus extending beyond the vent and reaching to the origin of the anal fin in C. minutum (Eigenmann, 1912)   , and reaching to or slightly beyond the anterior limit of the vent in C. ferreirai Vari, Ferraris & de Pinna, 2005   , C. morenoi (Fernández-Yépez, 1972)   , C. orientale (Vari, Ferraris & Keith, 2003)   , and C. pemon Vari, Ferraris & de Pinna, 2005   , the position of the vent (proximate to the base of the anterior most anal-fin ray versus distinctly anterior to that location in C. roae Vari, Ferraris & de Pinna, 2005   ), the form of the first rays of the dorsal and pectoral fins (with distal filaments present in males versus without such sexually-dimorphic filaments in C. ferreirai   ), the orientation of the dorsal and ventral profiles of the postdorsal portion of the body (converging posteriorly versus running in parallel in C. orientale   ), the distribution of dark pigmentation on the body (with pigmentation distributed across dorsal and lateral surfaces of body versus limited to middorsal region in C. ferreirai   ), the degree of dark pigmentation on the ventral surface of the lower jaw (with limited or no pigmentation versus with broad band of pigmentation in C. orientale   ), the form of the pigmentation on the head and body (chromatophores large and stellate versus small and round in C. minutum   and C. pemon   ), the extent of the pigmentation on the dorsal fin (without any pigmentation or at most several small dark basal spots versus with distinct semicircular dark spot basally in C. morenoi   , C. orientale   , and C. pemon   ), the body depth (0.17-0.18 versus 0.14-0.15 of SL in C. roae   ), and the form of the head in lateral view (triangular overall but relatively deep posteriorly versus more acutely triangular in C. minutum   [see Vari et al., 2005, fig. 3]).

Description. Body moderately robust, somewhat compressed anteriorly and becomes progressively distinctly compressed posteriorly. Body depth at dorsal-fin origin approximately 0.17- 0.18 [0.17] of SL, and approximately equal to distance from anterior margin of eye to rear of head. Lateral line on body unbranched, midlateral, incomplete, and extends from vertical through pectoral-fin base posteriorly to point within region from above middle of anal-fin base to slightly anterior to vertical through base of posterior most anal-fin ray. Dorsal profile of body straight from nape to dorsal-fin origin, slightly posteroventrally-aligned along base of dorsal fin and then straight from base of last dorsal-fin ray to caudal-fin base. Ventral profile of body slightly convex along abdomen, approximately straight and slightly converging posteriorly towards dorsal profile of body along anal-fin base. Caudalpeduncle depth greater than caudal-peduncle length.

Head relatively deep posteriorly, with lateral profile triangular overall but with bluntly pointed snout. Dorsal profile of head in male straight to slightly convex anteriorly, then straight to vertical located one orbital diameter posterior of rear margin of orbit, and finally broadly convex from that point to nape. Ventral profile of head variably convex. Head profile of female paratype deformed during preservation. Margin of snout in dorsal view broadly rounded. Postorbital margin of head slightly convex from dorsal view. Enlarged jaw musculature very evident on dorsal and lateral surfaces of postorbital portion of head.

Opercular membrane attached to isthmus only anterior of vertical through pectoral-fin insertion. Opercular opening moderately elongate; extends anteroventral of pectoral-fin insertion by distance approximately equal to one-third of head length and extends dorsal of pectoral-fin insertion by distance equal to horizontal extent of eye.

Eye situated on lateral surface of head; located dorsal to horizontal through pectoral-fin insertion; eye visible in dorsal view, but not in ventral view, of head. Middle of orbit at 0.36 [0.36] of HL. Eye diameter approximately one-third of length of snout. Interorbital width approximately equal to distance from tip of snout to point situated within region from middle of eye to posterior margin of orbit. Anterior narial opening circular, surrounded by short, anteriorly-directed, tubular rim of skin. Opening of anterior nares located slightly dorsal of horizontal that extends through maxillary-barbel origin and along horizontal that runs through ventral margin of orbit. Distance between anterior nares approximately equal to 1.5 orbital diameters. Posterior narial opening located on dorsal surface of head and situated dorsal to anterior one-third of orbit. Narial opening ovoid and bordered by flap of skin that nearly encircles aperture, but with small gap posteriorly; flap highest anterolaterally.

Mouth subterminal, very wide; its width 0.56 [0.56] of HL. Dorsal margin of lower jaw gently rounded, its posterior limit reaches to vertical through middle of orbit. Premaxillary tooth patch in form of gently arched band continuous across midline. Anterior margin of tooth patch convex and posterior margin concave and parallel to anterior margin. Teeth on premaxilla small, conical, sharply pointed, and uniform-sized across entire premaxilla, with three rows medially and two rows laterally. Palatal teeth in single arched row of 6 to 8 teeth, with distinct gap in series medially; gap approximately equal to one-half width of tooth patch on each side of palate. Palatal teeth conical, all of approximately uniform size, and with largest teeth approximately of same size as teeth on premaxilla. Dentary teeth comparable in shape to, and approximately same size as, premaxillary teeth, with three irregular rows medially that taper to one row laterally.

Maxillary barbel slender and extends posteriorly to point approximately one orbital diameter short of posterior margin of opercle. Barbel length approximately equal to length of postorbital portion of head, and approximately equal to twothirds of HL; barbel origin located ventral to anterior margin of orbit. Medial mental barbel slightly shorter than lateral mental barbel, with latter shorter than maxillary barbel. Medial mental-barbel origin located along vertical through rictus. Lateral mental-barbel origin situated slightly posterior of vertical through origin of medial mental barbel. Tips of adpressed mental barbels fall slightly short of, to barely beyond, opercular margin.

Dorsal-fin rays 6 [6]. Dorsal fin of moderate size, its base 0.35-0.36 [0.36] of HL. Longest branched dorsal-fin ray equal in length to slightly less than two-thirds of HL. Dorsal-fin spinelet present, first dorsal-fin ray spinous for basal onehalf of length and flexible more distally, with well-developed distal filament in mature male. Distal margin of dorsal fin slightly convex, with first branched ray longest. Dorsal-fin origin located at 0.33-0.35 [0.33] of SL and along vertical that extends through distal one-quarter of adpressed pectoral fin (leaving aside pectoral filament in male). Tip of adpressed dorsal fin in female reaches posteriorly to point slightly beyond tip of pelvic fin and slightly short of vertical through anterior margin of vent. Tip of distal filament of first ray in mature male reaches vertical through point approximately onethird length of anal-fin base from anal-fin origin. Last dorsal-fin ray with slight basal posterior membranous attachment to body.

Caudal fin deeply forked, symmetrical; tips of lobes rounded. Length of longest caudal-fin ray 2.25 [2.25] times length of middle rays.

Anal-fin rays 19-21 [21]. Anal-fin base moderately long. Anal-fin origin located distinctly posterior of middle of SL and approximately at middle of TL. Anal-fin margin nearly straight in female, but convex in mature male. Last anal-fin ray with slight membranous attachment to body.

Pelvic-fin rays i,5 [i,5]. Pelvic fin small; distal margin slightly convex with middle rays longest. Pelvic-fin insertion located anterior to middle of SL and slightly anterior of vertical through posterior limit of dorsal-fin base. Tip of adpressed pelvic fin extends to middle of SL but falls distinctly short of anterior margin of vent. Last pelvic-fin ray with membranous attachment to body along basal one-half of its length.

Pectoral-fin rays i,6 [i,6]. Pectoral fin moderately long, its length not including distal filament in male 0.53-0.54 [0.54] of HL. Pectoral-fin margin distinctly convex, with middle ray longest. First pectoral-fin ray spinous and slightly more than one-half length of first branched ray. Tip of first ray falling short of pelvic-fin origin in female, but prolonged as filament in mature male and reaching posteriorly to vertical running through point approximately at distal one-third of pelvic fin.

Coloration in alcohol. Overall ground coloration of head and body pale and overlain with rounded, large, brown chromatophores. Dark pigmentation on head well developed dorsally and in region posterior and posterodorsal to orbit. Scattered dark chromatophores present on lateral surface of snout, upper lip, and lower lip. Body distinctly darker dorsally, with expanded chromatophores in that region irregularly conjoined to form nearly uniform brown cast on portions of dorsal, dorsolateral and to varying degrees lateral surfaces of region posterior of vertical through insertion of anal fin. Dark pigmentation on body more pronounced in male. Ventral surface of body mostly pale other than for few scattered expanded chromatophores proximate to anal-fin origin.

Dorsal fin pale with some scattered dark chromatophores basally, but with that pigmentation not coalesced into distinct spot. Male with small flecks of dark pigmentation along length of spinous first ray; female with ray unpigmented. Anal fin pale with scattered dark chromatophores basally; chromatophores more numerous in male. Pelvic and pectoral fins pale. Caudal fin with dark chromatophores that form broad, posteriorly-convex band continuous with body pigmentation and overlying basal portions of caudal fin in male. Basal caudal-fin pigmentation less developed in female, with chromatophores in that specimen separated from each other and not extending as far distally onto fin rays.

Maxillary barbel with narrow, but distinct midlateral dark band on basal one-third to one-half and otherwise pale. Mental barbels pale overall, but with limited dark pigmentation basally in male.

Sexual dimorphism. The mature male of Cetopsidium soniae has an elongate filament extending from the tip of the first rays of the dorsal and pectoral fins. Such elaborations of these fins are characteristic of mature males of other species of Cetopsidium with the exception of C. ferreirai and occur in all adult males of all genera in the Cetopsinae other than for Denticetopsis Ferraris, 1996 (Vari et al., 2005). The male of Cetopsidium soniae has the anal-fin margin slightly convex rather than straight as in the female, another sexually dimorphic feature shared with mature males of the majority of species within the Cetopsinae with the exception of the members of Denticetopsis and some species of Cetopsis Spix & Agassiz, 1829 (Vari et al., 2005; de Pinna et al., 2007).

Distribution. Cetopsidium soniae   is known from the type locality in the Manari River, a tributary of the Takutu River in the western portions of the rio Branco system of the Amazon basin.

Habitat. At the time that the specimens were collected, the Manari River was approximately 1.5 m deep at the type locality with the substrate consisting of sand, gravel, and woody debris. Both the holotype and paratype were collected from holes in a large rock (S. Fisch-Muller, pers. comm.).

Etymology. The species name, soniae   , is in honor of Dr. Sonia Fisch-Muller of the Muséum d’histoire naturelle, Geneva, who brought the species to our attention, has been of invaluable assistance to both authors with a number of projects over the years, and has contributed in myriad ways to our knowledge of South American catfishes.

Barcodes. GenBank accession numbers for the nucleotide sequences are GQ141710 and GQ141711   .

Remarks. The combination of the presence of a dorsal fin retaining an ossified spinelet, the possession of pectoral and dorsal spines, and the termination of the lateral line posteriorly at a point above the base of the anal fin is unique to the species of Cetopsidium   within the Cetopsidae (Vari et al., 2005)   . All of these features are present in C. soniae   . Only one of these conditions, a lateral line that fails to extend past the vertical through the posterior terminus of the anal-fin base, was determined to be synapomorphic for the members of the genus under the phylogenetic hypothesis of relationships within the Cetopsidae   proposed by de Pinna et al. (2007). The remaining external features that serve in combination to diagnose Cetopsidium   (the presence of an ossified spinelet and possession of pectoral- and dorsal-fin spines) are symplesiomorphic within the Cetopsidae   according to the results of that analysis. The additional synapomorphies identified by de Pinna et al. (2007) for Cetopsidium   are internal features involving the first and third hypobranchials and the radials anterior to the anal-fin pterygiophores. The limited available sample of C. soniae   prevented confirmation of these osteological features in the species.

Cetopsidium roae   and C. pemon   also occur somewhat proximate to the type locality of C. soniae   in the upper rio Branco system. Cetopsidium roae   of the Rupununi River basin of the upper Essequibo River system of Guyana differs from C. soniae   in a number of features, most obviously in the

overall form of the head and body and pigmentation (compare

Fig. 1 View Fig with Vari et al., 2005, fig. 10). Vari et al. (2005) reported

Cetopsidium pemon   as a component of the ichthyofauna in

the Brazilian portions of the rio Branco basin and as such it is

the only member of the genus other than to C. soniae   known

from the rio Branco basin. As noted in the Diagnosis, C. soniae  

and C. pemon   differ in the posterior extent of the pelvic fin, the

form of the chromatophores on the head and body, and the

extent of dark pigmentation at the base of the dorsal fin.

Examination of a lot of Cetopsidium   from the Takutu River

system (ANSP 180959; Guyana, Rupununi (Region 9), Ireng

River, 04°01’10”N 59°36’06”W), revealed it to be C. pemon   .

This is the first record of the species from a location in Guyana.