Cíclidos México

Una nueva especie de incubador bucal de Gymnogeophagus con labios hipertrofiados

Andréia Turcati1 

Wilson Sebastián Serra-Alanis2 

Luiz R. Malabarba1  

1Programa de Pós-Graduação em Biologia Animal, Departamento de Zoologia, Universidade Federal do Rio Grande do Sul, Av. Bento Gonçalves 9500, 91501-970 Porto Alegre, RS, Brazil, (AT) bioturcati@gmail.com, (LRM) malabarb@ufrgs.br, https://orcid.org/0000-0002-9607-3735 (corresponding author)

2Sección Ictiología, Dpto. de Zoología, Museo Nacional de Historia Natural, CC 399, Montevideo, Uruguay. Centro Universitario Regional del Este (CURE), Sede Rocha, Ruta 15 y Ruta 9, Rocha, Uruguay, serraelbicho@gmail.com


A new mouth breeder species of Gymnogeophagus is described from a tributary of the río Uruguay. It is distinguished from most species of the genus by the presence of hypertrophied lips, and from G. labiatus and G. pseudolabiatus by the color pattern. The presence of successive allopatric species of the Gymnogeophagus gymnogenys clade inhabiting the tributaries of the río Uruguay is discussed.

Keywords: Distribution; Endemism; Gymnogeophagus gymnogenys clade; New species; Río Uruguay


Una nueva especie incubadora bucal de Gymnogeophagus es descripta de un tributario del Río Uruguay. Se distingue de la mayoría de las especies del género por la presencia de labios hipertrofiados, y de G. labiatus y G. pseudolabiatus por su patrón de coloración. Se discute la presencia de sucesivas especies alopátricas del clado Gymnogeophagus gymnogenys habitando los tributarios del Río Uruguay.

Palabras Clave: Distribución; Endemismo; Clado Gymnogeophagus gymnogenys; Especie nueva; Río Uruguay


Cichlidae constitutes one of the major vertebrate families, with more than 1,700 species (Fricke et al., 2018). The genus Gymnogeophagus Ribeiro is included in the tribe Geophagini (López-Fernández et al., 2005a2005b2010) along with approximately 14 other genera of the Neotropical subfamily Cichlinae. Species belonging to Gymnogeophagus are easily recognized by sharing two synapomorphies (Reis, Malabarba, 1988): the absence of supraneurals, and the presence of a forward-directed spine in the first pterygio phore of the dorsal fin (Fig. 1). Gymnogeophagus includes one extinct species, G. eocenicus Malabarba, Malabarba & Del Papa, 2010, known from fossil records of the Eocene Lumbrera Formation in northwestern Argentina, and 18 extant species from Paraná, Paraguay and Uruguay basins and small coastal drainages of Uruguay and southern Brazil, with one species, G. balzanii, also occurring in the rio Guaporé, Amazon drainage (Malabarba et al., 2015Loureiro et al., 2016Casciotta et al., 2017a).

Fig. 1 Anterior portion of dorsal-fin skeleton of Gymnogeophagus peliochelynion (anterior towards left), UFRGS 8076, paratype, 74.2 mm SL. Arrow indicates the anterior spine in the first dorsal pterygiophore. Note the lack of supraneurals between supraoccipital and first dorsal pterygio phore.

A brief review of the taxonomic and phylogenetic works dealing with Gymnogeophagus was given by Malabarba et al. (2015) and is not repeated here. Two major clades of Gymnogeophagus are recognized: one containing substrate breeder species, whose females deposit adhesive eggs on a surface and one or both parents guard and tend them, and another that includes mouth breeder species, where one or both parents brood orally the eggs and young (Reis, Malabarba, 1988Wimberger et al., 1998). The substrate breeder clade has been treated as the G. rhabdotus clade, G. rhabdotus species group or G. rhabdotus group (Malabarba et al., 2010Loureiro et al., 2016Říčanet al., 2018, respectively) and includes G. rhabdotus (Hensel, 1870), G. che Casciotta, Casciotta, Gómez & Toresanni, 2000, G. meridionalis Reis & Malabarba, 1988, G. setequedas Reis, Malabarba & Pavanelli, 1992, G. taroba Casciotta, Almirón, Piálek & Říčan, 2017, and G. terrapurpura Loureiro, Zarucki, Malabarba & González-Bergonzoni, 2016. The mouth breeder clade has been treated as the G. gymnogenys clade and G. gymnogenysgroup (Malabarba et al., 2010Říčan et al., 2018, respectively), and includes G. gymnogenys (Hensel, 1870), G. australis (Eigenmann, 1907), G. balzanii (Perugia 1891), G. caaguazuensis Staeck, 2006, G. constellatusMalabarba, Malabarba & Reis, 2015, G. labiatus (Hensel, 1870), G. lacustris Reis & Malabarba, 1988, G. lipokarenos Malabarba, Malabarba & Reis, 2015, G. mekinos Malabarba, Malabarba & Reis, 2015, G. missioneiroMalabarba, Malabarba & Reis, 2015, G. pseudolabiatus Malabarba, Malabarba & Reis, 2015, and G. tiraparaeGonzález-Bergonzoni, Loureiro & Oviedo, 2009. In this paper we describe a new species of the G. gymnogenysclade from a tributary of the lower río Uruguay, the río Arapey Grande.


Examined material of Gymnogeophagus belong to the fish collections of the Museu de Ciências e Tecnologia, Pontifícia Universidade Católica do Rio Grande do Sul, Porto Alegre (MCP), Museo Nacional de Historia Natural, Montevideo (MHNM), Universidade Federal do Rio Grande do Sul, Porto Alegre (UFRGS), and Facultad de Ciencias de la Universidad de la República, Montevideo (ZVC-P). Additional comparisons were done using data or specimens listed by Reis, Malabarba (1988), González-Bergonzoni et al. (2009), Malabarba et al. (2015) and Loureiro et al. (2016). Counts and measurements were taken according to Malabarba et al. (2015) and asterisks represents counts from the holotype. Specimens listed as non-types are referred for geographical distribution record, and were not counted or measured for species description. The localities of collection of specimens listed under Comparative material session are also given for distributional purposes.

Gymnogeophagus peliochelynion , new species

Figs. 15

Holotype. ZVC-P 12493, male, 101.9 mm SL, Uruguay, Salto, arroyo de las Tunas on Ruta 31, tributary to río Arapey Grande, 31°20’4.87”S 57°19’36.42”W, 8 Sep 2005, V. Bertaco, F. Cantera, J. Ferrer & L. R. Malabarba.

Paratypes. Uruguay, Departamento de Salto. Río Arapey drainage: MHNM 3711, 4, 1 male 79.9 mm SL, 3 females or juveniles 50.0-69.5 mm SL, río Arapey Chico on Ruta 4, 31°2’7.44”S 56°53’50.21”W, 22 Nov 2005, F. Teixeira, A. D’Anatro, I. González, S. Oviedo & M. Loureiro. UFRGS 8042, 7, 2 males 93.1-106.1 mm SL and 5 unsexed juveniles 19.7-64.1 mm SL, tributary stream to río Arapey Grande on Ruta 4, 31°07’44.0”S 56°59’57.0”W, 8 Sep 2005, V. Bertaco, F. Cantera, J. Ferrer & L. R. Malabarba. UFRGS 8076, 14, 3 males 99.7-100.1 mm SL (1 c&s 74.2 mm SL), 2 females 74.3-77.2 mm SL and 9 unsexed juveniles 51.2-67.1 mm SL (1 c&s 40.8 mm SL), collected with the holotype. UFRGS 8101, 1, female 70.3 mm SL, stream on Ruta 4, tributary of stream Valentin Grande, 31°16’32.0”S 57°09’22.0”W, 8 Sep 2005, L. R. Malabarba, V. Bertaco, J. Ferrer & F. Cantera. ZVC-P 13084, 4, 2 males, 76.4-79.7 mm SL, 2 females or juveniles 46.4-55.6 mm SL, Cañada de la Tapera, tributary of río Arapey, 31°09’02.15”S 56°13’25.18”W, 13 Dec 2014, M. Loureiro, A. Duarte, S. Serra, J. Bessonart & S. Paullier. ZVC-P 13210, 1 male 76.3 mm SL, río Arapey, Colonia Lavalleja, Paso Elías, 31°02’50.94”S 57°00’46.04”W, 17 Dec 2014, M. Loureiro, A. Duarte, S. Serra, J. Bessonart, S. Paullier.

Non-types: Uruguay, Departamento de Salto. Río Arapey drainage: ZVC-P 7016, 16, 43.3-94.1 mm SL, Río Arapey Chico, Ruta 4, 31°02’07.44”S 56°53’50.21”W, 22 Nov 2005, F. Teixeira, A. D’Anatro, I. González, S. Oviedo & M. Loureiro. ZVC-P 12656, 3, 48.9-59.0 mm SL, Arroyo Sopas, Paso del Cementerio, 31°23’34.21”S 56°42’31.06”W, 13 Aug 2013, M. Loureiro, J. Bessonart, S. Serra & L. Montes de Oca. ZVC-P 12715, 4, 44.6-61.6 mm SL, Arroyo Sauce del Arapey, 31°19’27.25”S 56°37’24.55”W, 11 Aug 2013, M. Loureiro, J. Bessonart, S. Serra & L. Montes de Oca. ZVC-P 13013, 1, 51.7 mm SL, Arroyo Mataperros, 30°58’47.46”S 56°23’15.60”W, 15 Dec 2014, M. Loureiro, A. Duarte, S. Serra, J. Bessonart & S. Paullier. ZVC-P 13043, 4, 43.9-59.4 mm SL, Arroyo Arerunguá, Paso del Potrero, 31°27’07.02”S 56°50’37.01”W, 18 Dec 2014, M. Loureiro, A. Duarte & S. Serra. ZVC-P 13057, 2, 65.3-90.2 mm SL, Arroyo Sopas, Paso del Cementerio, 31°23’34.21”S 56°42’31.06”W, 18 Dec 2014, M. Loureiro, A. Duarte & S. Serra. ZVC-P 13079, 3, 57.6-77.1 mm SL, Arroyo Mataojo, Pueblo Fernandez, 31°10’37.01”S 56°21’56.54”W, 14 Dec 2014, M. Loureiro, A. Duarte, S. Serra, J. Bessonart & S. Paullier. ZVC-P 13118, 6, 56.3-77.2 mm SL, Río Arapey, Picada Sarandí, 31°03’52.47”S 56°22’44.84”W, 15 Dec 2014, M. Loureiro, A. Duarte, S. Serra, J. Bessonart & S. Paullier. ZVC-P 13139, 2, 52.7-57.7 mm SL, Arroyo Mataojo Grande, Paso de la Herrería, 31°11’45.40”S 56°36’11.65”W, 14 Dec 2014, M. Loureiro, A. Duarte, S. Serra, J. Bessonart & S. Paullier. ZVC-P 13178, 3, 51.2-55.9 mm SL, Río Arapey, Colonia Lavalleja, Paso Elías, 31°02’50.94”S 57°00’46.04”W, 16 Dec 2014, M. Loureiro, A. Duarte, S. Serra, J. Bessonart & S. Paullier.

Diagnosis. The new species can be distinguished from the species of the Gymnogeophagus rhabdotus group and from G. balzanii by the shape of the caudal peduncle longer than deep (vs. deeper than long). It is distinguished from all congeners, except G. labiatus and G. pseudolabiatus, by the possession of thick lips. It differs from G. labiatus and G. lacustris by the lack of an oblique bar from the eye to the dorsal-fin origin (vs. oblique bar present), and by the color pattern of the caudal, dorsal and anal fins with dots (vs. caudal fin and posterior portion of anal fin with longitudinal hyaline stripes). It differs from G. pseudolabiatus and G. mekinos by the hump entirely black in males (Fig. 2vs. yellow with black margin), and upper lip not folded dorsally over anterior margin of snout (vs. upper lip folded dorsally, usually with a well-developed medial lobe dorsally projected in G. pseudolabiatus).

Fig. 2 Head of Gymnogeophagus peliochelynion (first column), G. pseudolabiatus (second column) and G. mekinos (third column) showing the entirely black hump in males in G. peliochelynion (vs. yellow with black margin), and upper lip not folded dorsally over anterior margin of snout (vs. upper lip folded dorsally in G. pseudolabiatus and undeveloped in G. mekinos). G. peliochelynionfrom top to bottom, paratype, ZVC-P 13210, paratype, 76.3 mm SL; ZVC-P 7016, 89.9 mm SL; ZVC-P 13057, 90.2 mm SL. G. pseudolabiatus from top to bottom, paratype, UFRGS 7754, 102.0 mm SL; MHNM 4010, 88.8 mm SL; MHNM 4010, 95.3 mm SL. G. mekinos from top to bottom, MHNM 3511, 105.1 mm SL; MHNM 3511, 97.2 mm SL; MHNM 4009, 121.3 mm SL.

Description. Standard length of specimens examined 19.2 to 106.1 mm. Morphometric data summarized in Tab. 1. Body elongated, laterally compressed. Dorsal profile of head slightly convex between mouth and interorbital area in young and females, slightly straight in males; slightly convex from interorbital region to dorsal-fin origin. Reproductive males with adipose hump from interorbital region to dorsal-fin origin; dorsal-fin base gently convex. Caudal peduncle rectangular, longer than deep, with slightly concave dorsal and ventral profiles. Prepelvic contour straight to slightly convex; abdominal contour straight and base of anal fin straight to slightly convex.

Tab. 1 Morphometric data of Gymnogeophagus peliochelynion, new species. Standard length is expressed in mm. Range includes measurements of holotype and 22 paratypes, except individuals smaller than 45 mm SL.

Holotype Min Max Mean SD
Standard length (mm) 101.9 46.42 106.08 73.87
Percent of standard length
Head length 38.3 35.0 39.2 36.8 1.07
Body depth 38.5 33.8 39.9 37.7 1.44
Dorsal-fin base length 48.2 45.4 54.1 50.3 2.05
Pectoral-fin length 33.6 30.1 39.3 34.4 3.19
Caudal peduncle depth 13.2 11.9 14.2 13.3 0.52
Caudal peduncle length 15.1 14.0 18.1 15.3 1.10
Percent of head length
Eye diameter 21.3 20.2 32.3 25.1 3.27
Interorbital width 28.5 24.6 32.4 28.0 1.97
Upper jaw length 26.7 19.7 29.7 23.5 3.39
Pre-orbital length 33.4 26.9 36.6 30.7 2.83
Snout length 57.7 30.5 59.7 46.4 7.64

Head depth larger than head length. Snout triangular in lateral aspect; slightly rounded anteriorly, pointed in dorsal aspect. Eyes small, close to dorsal profile of head in juveniles and progressively farther from it in larger specimens (about eye diameter in specimens up to 80 mm); eyes near middle of head length. Interorbital area slightly convex in young and female, and deeply convex in large males; interorbital width larger than eye diameter, except in individuals smaller than 25 mm. Mouth terminal. Posterior tip of ma xilla not reaching vertical line across anterior margin of eyes. Upper jaw slightly longer than lower jaw; lips developed, lower lip thicker than upper lip; margin of lower lip convex, deeper in middle length of each dentary, deeply notched medially at symphysis. Snout longer than postorbital length, except in individuals up to 48 mm SL.

Body scales moderately large and ctenoid, smaller ctenoid scales in preventral area. Proximal third to half of caudal fin with small elongated cycloid scales in single series between contiguous rays. Dorsal fin without scales. Cheek naked. Small cycloid scales on opercle. Subopercular scales ctenoid in 1-2 irregular rows. Ctenoid scales on base of hump (in adult reproductive males only) to approximately vertical line passing on anterior margin of eye. Scales in longitudinal series 26*(5), 27(6), 28(3). Anterior lateral line 15(1), 17*(8), 18(5). Posterior lateral line 8*(4), 9 (6), 10(1), 11(2), 12(1). Scales between anterior lateral line and dorsal fin 6*(12), 7(2). Scales between anterior lateral line and anal fin 8*(11), 9(3).

Dorsal-fin spines 12(1), 13(2), 14*(11); dorsal-fin soft rays 9(1), 10*(11), 11(2). First dorsal-fin spine inserted right above vertical line across posterior bony margin of opercle. Soft dorsal fin slightly pointed in young and adult females, reaching or almost reaching caudal-fin base. Fourth or fifth dorsal-fin soft ray longest in mature males, reaching proxi mal two third to half of caudal-fin length. Three anal-fin spines; anal-fin soft rays 8*(11), 9(3); anal-fin profile rounded in young and females, reaching or almost reaching caudal-fin base; slightly pointed in reproductive males, surpassing caudal-fin base. Pectoral fin with pointed tip, reaching or almost reaching anal-fin origin in juveniles and females and surpassing anal-fin origin in reproductive males. Pelvic fin slightly pointed; second soft ray longest, reaching anal-fin base in mature males. Caudal-fin margin concave.

Jaw teeth small, conical, with recurved tips. Upper jaw with outer regular row of 16-26 teeth in each premaxilla (number increasing with specimen size) and two irregular internal rows of slightly smaller teeth. Lower jaw with 3-5 irregular rows of small conical teeth; outer hemiseries with 20-28 teeth. Lower limb of first gill arch with 6-10 gill rakers; upper limb lobed with 3-4 gill rakers in its margin. Lower pharyngeal tooth plate wide; teeth covering whole occlusion surface. Teeth on medial rows larger than remaining ones. Posterolateral teeth elongated; posteromedial teeth larger, cylindrical with medial, blunt cusps of molariform aspect (Fig. 3).

Fig. 3 Pharyngeal tooth plate of Gymnogeophagus peliochelynion, 74.2 mm SL, UFRGS 8076, paratype. Dorsal view; anterior to bottom.

Coloration after fixation in formalin. (Fig. 4) Mature males: ground color of body dark brown above longitudinal series of scales of posterior lateral line and light yellowish brown below. Series of double vertical bars clearly discernible along midventral lateral surface of flanks, distributed between pectoral-fin base and end of caudal peduncle, anterior to caudal-fin base. Number of vertical double dark bars 5-6. Midlateral spot without defined borders. Hump entirely black in males making dark band in front of dorsal-fin origin hardly detectable. Head dark brown with some black spots on cheek and near posterior margin of opercle; dark band covering cheek hardly distinct. Isthmus and branchiostegal membranes dark brown. Pectoral fin hyaline. Pelvic fin dark gray. Spinous dorsal fin dark brown; soft dorsal fin light brown with circular dots. Distal one third of anal-fin rays and spines dark brown, without additional marks. Two proximal thirds of anal-fin rays covered with small circular dots. Caudal fin covered with white dots, except near upper and lower borders.

Color in alcohol of preserved females and young not distinct from that described for males. Main differences are: isthmus and branchiostegal membrane yellow; clearly distinct dark band covering cheek, below eye; distinct dark band on dorsal-fin origin; and larger size of white spots on dorsal, anal, and caudal fins.

Fig. 4 Gymnogeophagus peliochelynion: top, holotype, male, ZVC-P 12493, 101.9 SL; bottom, paratype, female, UFRGS 8076, 77.2 SL. Both from arroyo de las Tunas on road 31, tributary of río Arapey Grande, Salto, Uruguay. Photographs taken just after collection and fixation in formalin.

Coloration in life. (Fig. 5) Ground color of dorsal profile golden or dark olivaceous with longitudinal series of light blue spots. Well defined black, circular midlateral spot, covering scales 9-11 of the anterior lateral line, scales 10-12 of the scale row just below anterior lateral line and scales 8-10 of the next scale row below. Large dark bar below eye, usually not reaching midline of mouth in larger individuals. Numerous small bright blue spots usually present on cheeks. Red marks on cheeks usually present in mature males, concentrated on upper portion of opercle and preopercle, region behind eye and above pectoral fin. Usually grayish blue lips in reproductive males and gray in females and young. Adipose hump, when present, black. Ventral portion of body light olivaceous to yellow pale in mature males with longitudinal series of light blue spots. Spinous dorsal fin and base of soft dorsal fin yellowish brown; most soft dorsal fin red with relatively large and numerous hyaline dots. Distal tip of dorsal fin hyaline. Pectoral fin hyaline and pelvic fin dark orange to dark gray with light blue spots at base. Anal fin yellowish orange proximally with numerous clear spots and hyaline on half distal portion with dark gray margin. Caudal fin yellowish brown with numerous light spots, extending along middle of caudal fin; dorsal and ventral portions of fin hyaline.

Fig. 5 Gymnogeophagus peliochelynion: above, paratype, male, ZVC-P 13210, paratype, 76.3 mm SL, río Arapey, Colonia Lavalleja, Paso Elías, Salto, Uruguay; below, female, ZVC-P 13057, 65.3 mm SL, Arroyo Sopas, Paso del Cementerio, Salto, Uruguay. Photographs of live specimens.

Geographic distribution. This species is known from the río Arapey Grande drainage, a tributary of the lower río Uruguay basin, Uruguay (Fig. 6).

Fig. 6 Geographic distribution of Gymnogeophagus peliochelynion (yellow; star refers to type locality), G. cf. peliochelynion(orange) and other species of the Gymnogeophagus gymnogenys clade: G. lipokarenos (blue), G. constellatus (green), G. missioneiro (red), G. tiraparae (white), G. mekinos (black), G. pseudolabiatus (pink) in the río Uruguay basin. Records of Gymnogeophagus lipokarenos and Gymnogeophagus constellatus from Argentina (triangles) are based on Casciotta et al. (2017b) and Říčan et al. (2017), respectively.

Ecological notes. The new species was collected in rivers with clear water, usually with rocky or muddy bottom and little vegetation.

Etymology. The name peliochelynion is from the Greek pelios, meaning black and blue, and chelyne, meaning lip, in reference to the color of the lips of the new species. A name in apposition.

Conservation status. Gymnogeophagus peliochelynion is relatively frequent and abundant in the río Arapey Grande drainage. No specific threats were detected, and the species can be categorized as Least Concern (LC) according to IUCN criteria (IUCN, 2016).


Gymnogeophagus peliochelynion shares the two synapomorphies that diagnoses the genus (Reis, Malabarba, 1988): the lack of supraneurals and the presence of a forward-directed spine on anterodorsal margin of the first dorsal-fin pterygiophore (Fig. 1). The new species also belong to a clade that includes G. gymnogenys. Species in this clade are easily recognized by sharing two synapomorphies (more easily observed in females and juveniles; Fig. 5): the absence of an oblique bar between the dorsal border of the eye and the nape, and the possession of a black bar originating in the dorsal contour near the dorsal-fin origin and directed downward and backward on the dorsum (Reis, Malabarba, 1988Malabarba et al., 2015). The conspicuous secondary sexual dimorphism (including development of a nuchal hump in reproductive males), mouthbrooding reproductive strategy, and elongated caudal peduncle, longer than deep (Wimberger et al., 1998), which are not observed in the G. rhabdotus group, further support the inclusion of G. peliochelynion in the Ggymnogenys clade.

Species of the Gymnogeophagus gymnogenys clade have an allopatric distribution (Fig. 6) along several tributaries of the río Uruguay (Malabarba et al., 2015Casciotta et al., 2017bŘíčan et al., 2017). Gymnogeophagus lipokarenos is endemic to the upper portion of the río Uruguay, upstream to San Javier (Argentina)/Porto Xavier (Brazil). Gymnogeophagus constellatus and Gmissioneiro occur in tributaries immediately downstream of San Javier and Porto Xavier , the first occurring mainly in the rio Ijuí (Brazil), arroyo Itacaruaré and arroyo Chimiray-Miní (Misiones) drainages, and the second occurring in rio Piratini (Brazil) drainage, all draining a basaltic rock bed of the Serra Geral Formation (Batezelli et al., 2005). The next main tributary of the Río Uruguay, in a downstream direction, is the rio Ibicuí, with a fine grain sedimentary substrate, corresponding to the unique tributary of the middle Río Uruguay where G. tirapa rae and G. mekinos are found. These two species are present too in lower tributaries of Uruguay and La Plata river basins in Uruguay and Brazil. In the next downstream drainage, the rio Quaraí, with basaltic rock bed, we find Gpseudola biatus. The next downstream tributary, the río Arapey, is occupied by the new species described herein, G. peliochelynion. This successive substitution of allopatric species of the Gymnogeophagus gymnogenys clade along río Uruguay tributaries suggests the main channel act as a physical or ecological barrier to dispersal of these species, all of which are adapted to small affluents. Similar patterns have been observed in the tributaries of the rio Amazonas for other groups of fish (Junk et al., 2001Hubert, Renno 2006) and for Atlantic coastal rivers connected though freshwater lakes (Hirschmann et al., 2015).

Populations from río Queguay and río Dayman located downstream from the río Arapey are tentatively identified herein as G. cf. peliochelynion. Although they do not show hypertrophied lips, they show similar color pattern to that described for G. peliochelynion. Further investigation is needed in order to determine whether these populations cons titute a separate species.

Comparative material examined (In addition to those listed by Malabarba et al., 2015). Gymnogeophagus cf. peliochelynion. Uruguay, Departamento de Salto. Río Dayman drainage: ZVC-P 6686, 1, 57.7 mm SL, río Dayman, Ruta 4, 31°47’15.45”S 57°02’12.24”W, 21 Nov 2005, M. Loureiro, F. Teixeira, S. Oviedo, A. D’Anatro & I. González. ZVC-P 13242, 1, 54.2 mm SL, Río Dayman, Paso Morales, 31°28’40.92”S 57°49’40.14”W, 17 Dec 2014, M. Loureiro, S. Serra & A. Duarte. Departamento de Paysandú. Río Queguay drainage: ZVC-P 13299, 1, 53.7 mm SL, Río Queguay, Paso del Sauce, 32°16’55.46”S 56°45’17.24”W, 19 Dec 2014, A. Duarte, S. Serra & M. Loureiro. ZVC-P 13306, 1, 70.5 mm SL, Arroyo Corrales, Paso Castillo, 31°56’29.54”S 56°37’12.40”W, 19 Dec 2014, A. Duarte, S. Serra & M. Loureiro. ZVC-P 13348, 1, 48.5 mm SL, Río Queguay, Cerro del Inglés, 32°10’31.73”S 57°44’00.01”W, 19 Apr 2015, S. Paullier, J. Cabrera, M. Trillo, M. Loureiro & J. Bessonart. ZVC-P 13367, 1, 108.3 mm SL, Arroyo Ñacurutú Grande, 32°18’39.78”S 57°24’20.88”W, 21 Apr 2015, S. Paullier, J. Cabrera, M. Trillo, M. Loureiro & J. Bessonart. ZVC-P 13387, 1, 65.8 mm SL, Río Queguay Chico, Paso del Parque, 32°٠2’27.76”S 56°59’26.24”W, Apr 2015, S. Paullier, J. Cabrera, M. Trillo, M. Loureiro & J. Bessonart. ZVC-P 13439, 1, 67.7 mm SL, Arroyo Bacacuá Grande, 32°19’12.30”S 57°36’16.66”W, 21 Apr 2015, S. Paullier, J. Cabrera, M. Trillo, M. Loureiro & J. Bessonart. Gymnogeophagus gymnogenys. Brazil, Rio Grande do Sul State (all from laguna dos Patos draina ge): UFRGS 4242, 10, 47.3-65.4 mm SL, arroio Velhaco; UFRGS 13697, 1, 106.3 mm SL, arroio Forquetinha; UFRGS 14213, 8, 39.9-94.8 mm SL, arroio Forquetinha; UFRGS 16135, 1, 88.1 mm SL, lago Guaíba; UFRGS 16136, 1, 92.4 mm SL, lago Guaíba. Gymnogeophagus mekinos. Uruguay, Departamento de Florida. MHNM 3511, 2, 97.2-105.1 mm SL, Paso de la Arena, Río Santa Lucía Chico, 34°01’51.24”S 56°09’45.75”W, 11 Jan 2014, W.S. Serra & M. Pérez. Departamento de Rocha. MHNM 4009, 4, 49.9-121.3 mm SL, Arroyo Rocha, Parque La Estiva, Ciudad de Rocha, 34°29’38.43”S 54°20’43.58”W, 22 Jan 2018, W.S. Serra. Gymnogeophagus pseudolabiatus. Uruguay, Departamento de Artigas. MHNM 4010, 7, 55.3-95.3 mm SL, Arroyo Pintado y Ruta 30, 30°26’16.70”S 56°26’59.23”W, 2 Dec 2017, W.S. Serra & N. Ríos; ZVC-P 9893, 5, 34.9-88.2 mm SL, Cañada Mataojo, 30°47’46.93”S 56°56’52.66”W, Aug 2006, M. Loureiro, F. Teixeira, I. González & F. Quintans; ZVC-P 10011, 11, 24.8-87.4 mm SL, Cañada Honda, 30°27’46.98”S 56°51’24.82”W, Aug 2006, M. Loureiro, F. Teixeira, I. González & F. Quintans; ZVC-P 10057, 27, 28.1-80.9 mm SL, Cañada Honda, 30°27’33.47”S 56°49’51.29”W, Aug 2006, M. Loureiro, F. Teixeira, I. González & F. Quintans; ZVC-P 12616, 7, 46.6-93.2 mm SL, Cuareim River, Laguna Salamanca, 30°46’36.21”S 56°02’16.71”W, Dec 2012, A. Duarte, W.S. Serra, M. Loureiro & L. Ziegler; ZVC-P 12684, 2, 98.2-101.6 mm SL, Cuaró Grande stream, Ruta 4, 30°46’57.96”S 56°47’05.08”W, Aug 2013, M. Loureiro, J. Bessonart, W.S. Serra & L. Montes de Oca.


We are grateful to the following colleagues and their institutions for the loan of specimens: Carlos A. S Lucena (MCP) and Marcelo Loureiro (ZVC-P). We are grateful to Néstor Ríos, Cristhian Clavijo, Alejandro Duarte, Marcelo Loureiro, Sofía Paulier, Mauricio Pérez, Juliano Ferrer, Vinícius Bertaco, and Felipe Cantera for their assistance with fieldwork and to Mayara Neves for the photo of Fig. 3. LRM is partially financed by CNPq (307890/2016-3; 401204/2016-2).


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