Reproductive biology and feeding of Curimatella lepidura (Eigenmann & Eigenmann) (Pisces, Curimatidae) in Juramento reservoir, Minas Gerais, Brazil

Biologia reprodutiva e alimentação de Curimatella lepidura (Eigenmann & Eigenmann) (Pisces, Curimatidae) no reservatório de Juramento, Minas Gerais, Brasil

Reproductive biology and feeding of Curimatella lepidura (Eigenmann & Eigenmann) (Pisces, Curimatidae) in Juramento reservoir, Minas Gerais, Brazil

Biologia reprodutiva e alimentação de Curimatella lepidura (Eigenmann & Eigenmann) (Pisces, Curimatidae) no reservatório de Juramento, Minas Gerais, Brasil

Érika R. de Alvarenga^I; Nilo Bazzoli^{I, II}; Gilmar B. Santos^II; Elizete Rizzo^I,1

^IDepartamento de Morfologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais. Caixa Postal 486, 30161-970 Belo Horizonte, Minas Gerais, Brasil. E-mail: [e-mail]

^IIPrograma de Pós-Graduação em Zoologia de Vertebrados, Pontifícia Universidade Católica de Minas Gerais. 30535-610 Belo Horizonte, Minas Gerais, Brasil. E-mail: [e-mail]

ABSTRACT

Reproductive biology and feeding of Curimatella lepidura (Eigenmann & Eigenmann, 1889) were studied in Juramento reservoir, São Francisco River basin, Southeastern Brazil. Histological analyses and gonadosomatic indexes revealed females and males in reproductive activity from October to March and total spawning occurring from January to March coupled with the peak of spermiating males. In the dry season, the fishes accumulated energetic reserves for reproduction during a short rainy season. The species presented sexual dimorphism, being females larger than males and sexual maturation occurring close to 7.7 cm standard length for females and 7.1 cm for males. C. lepidura presented iliophagous feeding habit, ingesting mainly sediment/detritus and a small amount of acari, algae, Tricoptera insects and Ostracoda crustaceans, suggesting a probable role in nutrient recycling of the Juramento reservoir.

Key words: Diet; gonadal maturation; reproduction; São Francisco River; spawning.

RESUMO

A biologia reprodutiva e alimentação de Curimatella lepidura (Eigenmann & Eigenmann, 1889) foram estudadas no reservatório de Juramento, Bacia do rio São Francisco, Sudeste do Brasil. Análises histológicas e índices gonadosomáticos mostraram fêmeas e machos em atividade reprodutiva de outubro a março e desova total ocorrendo de janeiro a março coincidindo com pico de espermiação. Na estação seca, os peixes acumularam reservas energéticas para a reprodução durante curta estação chuvosa. A espécie apresentou dimorfismo sexual, sendo as fêmeas maiores do que os machos e, a maturação gonadal ocorreu em torno de 7,7 cm de comprimento padrão para as fêmeas e 7,1 cm para os machos. C. lepidura apresentou hábito alimentar iliófago, ingerindo predominantemente sedimento/detrito e, em menor proporção, ácaros, algas, insetos Tricoptera e crustáceos Ostracodas sugerindo provável papel na reciclagem de nutrientes do reservatório de Juramento.

Palavras-chave: Desova; dieta; maturação gonadal; reprodução; Rio São Francisco.

Curimatidae family has geographic distribution restricted to South America and Southeastern Central America with representatives in different aquatic environments (NELSON 1994). Curimatella lepidura, known popularly as manjuba or saguiru, prefers lentic environments and is abundant in marginal lagoons of the São Francisco River basin (GOMES & VERANI 2003).

Damming imposes changes in the natural course of a river and may affect the biological functions of the fishes as reproduction, feeding, migration and growth, usually leading to extinction of some species and to abundance increasing of others (ALBRECHT & P-CARAMASCHI 2003). Basic biological information as feeding and reproduction are required in fish population studies with the purpose of conservation of native species and also for fish culture (GURGEL et al. 1995). Since species conservation and abundance depends on the reproductive success, knowledge of fish reproductive cycle in reservoirs is fundamental as it allows assessing if the populations remain viable (SUZUKI & AGOSTINHO 1997). Studies on diet are important to understand the dynamic of the fish communities, reflecting the role of each species in the ecosystem (SABINO & CASTRO 1990).

Although the dam of Juramento reservoir was concluded in 1981, studies on composition of its fish fauna (DABÉS et al. 2001) and reproductive biology (THOMÉ et al. 2005) are scarce. Studies on trophic ecology and reproduction of the main fish species have been carried out in Juramento reservoir since 2002. The present study is aimed at analysing the reproductive biology and diet of C. lepidura in this reservoir.

MATERIAL AND METHODS

The Juramento reservoir (16º45'-16º48'S; 43º41'-43º37'W) was built for supplying the Montes Claros city, Minas Gerais, Brazil. The reservoir has a flooded area of 7.6 Km², mean depth of 9.1 m and 45 x 10⁶ m³ of water, comprising the Canoas, Saracura and Juramento rivers from Verde Grande River, São Francisco River basin (DABÉS et al. 2001).

The reproductive biology of C. lepidura was studied with 161 females and 49 males quarterly captured in Juramento reservoir from April 2002 to March 2003, using gillnets with mesh sizes from 3 to 10 cm between opposite knots and soaking during 15 hours.

To preserve stomach contents and determine food resources ingested by C. lepidura, 50 specimens were captured in May, June, September and November 2002, using gillnets which were exposed during three hours only (5 to 8 PM).

Fishes caught were fixed in 10% formalin and later stocked in 70% alcohol. Standard length (SL) and body weight (BW) were obtained from each specimen. Fishes were dissected to obtaining the weights of the gonad (GW), stomach (SW), liver (LW) and coelomic fat (CFW). The following biological indexes were calculated for each specimen: gonadosomatic index (GSI = GW x 100/BW), hepatosomatic index (HSI = LW x 100/BW), stomach repletion index (SRI = SW x 100/BW), coelomic fat index (CFI = CFW x 100/BW) and Fulton condition factor (K = BW - GW x 100/SL³).

The specimens were grouped for classes of standard length and body weight and the relative frequencies were determined for each class. The length of the smallest male and female reproductively active was used to estimate the approximate size at first gonadal maturation (BAZZOLI 2003). Sexual ratio was determined for total sampling.

For histological analyses, gonad fragments were fixed in Bouin's fluid, embedded in paraffin, sectioned with 4-6 mm thick and stained with Hematoxylin-Eosin. Reproductive cycle stages were determined based on macro- and microscopic characteristics of the gonads and GSI values.

After specimens dissection, the degree of the stomach fullness was recorded as follows: empty (0); almost empty (1), half-full (2) and completely full (3). Uncoiled intestine length (IL) was obtained from 15 specimens to calculate the intestinal quotient (IQ = IL/SL) (BARBIERI et al. 1994).

In order to investigate the food resources consumed by C. lepidura, the gastric content from each specimen was analysed according to occurrence and volumetric methods under a stereomicroscope (HYSLOP 1980). Food items were identified up to the lowest possible taxonomic level and algae was identified under a light microscope. Food importance index (FI) was determined during rainy season (November) and dry season (May, June and September): FI = 100 OV. (S OV)^-1, where O = % occurrence and V = % volume (DELARIVA & AGOSTINHO 2001).

Temperature, pH, conductivity, water transparency and dissolved oxygen at water surface during the fish collections were supplied by COPASA (Companhia de Saneamento de Minas Gerais).

After performing the Kolmogorov-Smirnoff normality test, data were submitted to one-way ANOVA followed by a Tukey post-hoc test to compare means of biological indexes. Student's t test was used to analyse length and weight of males and females and sexual proportion was submitted to Chi-square test (c²). All tests were performed at significance level of 0.05.

RESULTS

Females of C. lepidura (6.9 to 13.2 cm SL and 12.2 to 77 g BW) were significantly larger than males (6.7 to 12.8 cm SL and 10 to 64 g BW). Most females had 11-12 cm SL and 50-60 g BW and most males had 10-11 cm SL and 30-40 g BW (Fig. 1). Sexual ratio of three females for each male was highly significant (c² test, with p < 0.001). The smallest female in advanced maturation had 7.7 cm SL and 17.6 g BW and the smallest male had 7.1 cm SL and 13.8 g BW.

In females, mean GSI was significantly higher while SRI and HSI were lower in October/November/December trimester (Tab. I). The same tendency was observed in GSI of males, although no significant difference had been detected between the trimesters. Females' CFI was higher from April to September decreasing to minimum at January/February/March trimester similar to males. Condition factor (K) presented some significant differences throughout the trimesters only for females.

Gonadal maturation was classified in four stages (Tab. II and Figs 2 to 9). Regarding the frequencies of reproductive cycle stages, resting stage was predominant from April to September (Fig. 10). Initial and advanced maturing stages were more frequent in October/November/December but also occurred in January/February/March trimester. Spawned females occurred in January/February/March only coupled with the peak of spermiated males. Brown-yellowish bodies constituted of cell aggregates storing pigments involved by a highly vascularised connective tissue were numerous during the ovarian recovery postspawning.

Higher dissolved oxygen and pH occurred at advanced maturation from October to December (Fig. 11). During spawning from January to March, water temperature and conductivity were higher and transparency was lower. The lowest pH, oxygen, temperature and conductivity were found at resting from April to June.

All sampled stomachs had some food, however the stomach repletion was higher in the dry season and, most stomachs were almost empty during the rainy season (Tab. III). Stomach contents included mainly sediment/detritus whereas Ostracoda (Crustacean), Tricoptera larvae (insect), algae Pleurotaenium ovatum (Nageli, 1849) (Desmidiaceae) and acari (Arachnida) were less found. Sediment/detritus was the most important food item (FI = 0.96 in the dry season and 0.99 in the rainy season), followed by Ostracoda (FI = 0.04 in the dry season and 0.01 in the rainy season). The other items presented volume less than 0.5 mm³ and then they were not used to calculate the FI. The IQ value for C. lepidura was 13.52 ± 4.24.

DISCUSSION

Size distribution indicated sexual dimorphism for C. lepidura, being females larger than males as also reported for other curimatids such as Steindachnerina elegans (Steindachner, 1875) in Tiête river (RODRIGUES et al. 1989) and Cyphocharax voga (Hensel, 1869) in Emboaba lagoon (HARTZ & BARBIERI 1994). Prevalence of females in sampling as also reported for S. elegans and C. voga (RODRIGUES et al. 1989, HARTZ & BARBIERI 1994) may be due to great probability of females being captured by the mesh size of the gillnets used during the fish collections. In the present study, immature fishes were not captured and, then the size of first gonadal maturation was not determined by L₅₀ method. However, the smallest specimen in advanced maturation (7.7 cm SL for females and 7.1 cm SL for males) may be an indicator of first gonadal maturation (BAZZOLI 2003). This parameter of the reproduction biology may avoid captures of the juveniles in order to conservation of the fish populations.

In the present work, GSI and reproductive cycle stages frequencies indicated gonadal maturation occurring mainly in October/November/December and spawning in January/February/March. Absence of partially spawned females and a short-term reproduction pattern indicated total spawning for C. lepidura. This non-migratory species with no parental care reproduces at Três Marias reservoir, exhibiting an extended reproductive period (SATO et al.2003). Other authors also reported that species of Curimatidae family are generally characterised by a long reproductive period (RODRIGUES et al. 1989, HARTZ & BARBIERI 1994, SCHIFINO et al. 1998). Probably due to the short rainy season, spawned females were captured at the Juramento reservoir during January/February/March only and, all females were found in resting in the following trimester.

Unlike the females, testicular maturation and spermiation were prolonged in C. lepidura, as also occur in other species of total spawning such as Leporinus reinhardti Lütken, 1874 (RIZZO et al. 1996) and Pseudoplatystoma corruscans (Spix & Agassiz, 1829) (BRITO & BAZZOLI 2003). Despite the males to be apt to reproduction for a longer period than the females, the spermiation peak is coupled with spawning.

In the present study, GSI peak associated to decreasing of HSI at advanced maturation suggest liver participation in the vitellogenin synthesis and mobilisation of energetic reserves for reproduction since the feeding activity is reduced or interrupted during reproduction in accordance with other authors (HTUN-HAN 1978, AGOSTINHO et al. 1990, BAZZOLI & GODINHO 1991, TAVARES & GODINHO 1994, BENNEMANN et al. 1996). Higher CFI in resting period decreasing during the advanced maturation indicated energetic consume for concluding the reproductive activity, which was compensated by a greater feeding activity at resting similar to other Characiformes (NOGUEIRA et al. 1997, BARRETO et al. 1998, BRITO et al. 1999, HOJO et al. 2004). According to BARBIERI & VERANI (1987) high K values happen simultaneously to GSI peak in advanced maturation and low K coincided with low GSI and high frequency of females in resting stage. However, K values were few significant in C. lepidura due probably to its feeding habit.

In the present work, reproduction of C. lepidura occurred during the period of highest temperature as also reported for other Characiformes (HARTZ & BARBIERI 1994, BAZZOLI et al. 1998, NOGUEIRA et al. 1997, RICARDO et al. 1997). Temperature regulates the reproductive process acting in specific thermoreceptors or through effects on the metabolism and growth. Higher temperatures cause an increase in the pituitary response to the hypothalamic factor increasing gonadotrophin release, which, in its turn, induces gonadal recrudescence (QUINTANA et al. 2004). Rain may alter water parameters causing an increase in oxygen, pH and conductivity levels and a decrease in the transparency due to the allochthonous materials (PINTO et al. 2003). In accordance with BAZZOLI (2003), rainfall is the best stimulus to spawning, usually acting in fish reproduction due to a higher oxygenation at the water surface, where most of the eggs and newly-hatched larvae are found in suspension.

Regarding the feeding habit, C. lepidura was previously considered an iliophagous or detritivorous species (GOMES & VERANI 2003). However, according to HAHN et al. (1997), sediment and detritus are considered distinct categories and detritivorous fish present feeding composed usually of large particles along with dead arthropod and invertebrate exuviae. In the present study, C. lepidura presented an iliophagous feeding habit ingesting mainly sediment associated with a small amount of detritus. Species from this trophic category explore the bottom or the periphyton, ingesting a great quantity of sediment associated with unicellular algae and micro organisms and organic matter in fine particles (AGOSTINHO et al. 1997). Mechanisms employed by fish for its diet, represent adaptations, which make them able to use a specific kind of prey (LUNARDON-BRANCO & BRANCO 2003). As an adaptation to the iliophagous habit, the digestive tract of C. lepidura presents a mechanic stomach similar to gizzard and long-coiled intestine for a better utilisation of food and does not present teeth in the maxillary (Agostinho et al. 1997, Gomes & Verani 2003). Moreover, the long coiled intestine found in C. lepidura is characteristic of the detritivorous fish, being intestine length related directly to food digestibility and quantity of detritus (DELARIVA & AGOSTINHO 2001).

In present study, C. lepidura, has ingested Ostracoda during the dry season, but sediment/detritus was predominant along all year. Analysis of stomach repletion index has shown greater feeding activity in the dry season, coinciding with resting period, when fish accumulate energetic reserves for the reproductive activity. Differences in the abundance of food between dry and rainy seasons affect directly the tropical fish communities. As a response to these variations, opportunistic species change their diet according to the food availability (POMPEU 1999). However, the morphological adaptations of the digestive tract of some trophic categories like the iliophagous fishes including C. lepidura, make these species highly specialised and impose limits on diet changing (AGOSTINHO et al. 1997).

ACKNOWLEDGMENTS

This paper is result of a project financed by COPASA with support of the CNPq, FAPEMIG, and FIP-PUC Minas. The authors are grateful to: Mônica Ladeia (COPASA) and Maria B. Gomes (UNIMONTES), Guilherme R. Medeiros, André R. M. Silva, and Valdeir; Marcos Cabral de Melo by algae identification.

Received in 16.VI.2005; accepted in 28.III.2006.

• ¹
  ALBRECHT, M.P. & E. P.-CARAMASCHI. 2003. Feeding ecology of Leporinus taeniofasciatus (Characiformes: Anostomidae) before and after installation of a hydroelectric plant in the upper rio Tocantins, Brazil. Neotropical Ichthyology, Porto Alegre, 1 (1): 53-60.
• AGOSTINHO, A.A.; G. BARBIERI; J.R. VERANI & N.S. HAHN. 1990. Variação do fator de condição e do índice hepatossomático e suas relações com o ciclo reprodutivo em Rhinelepis aspera (Agassis, 1829) (Osteichthyes, Loricariidae) no rio Paranapanema, Porecatu, PR. Ciência e Cultura, São Paulo, 42 (9): 711-714.
• AGOSTINHO, A.A.; N.S. HAHN; L.C. GOMES & L.M. BINI. 1997. Estrutura trófica, p. 229-248. In: A.E.A.M. VAZZOLER; A.A. AGOSTINHO & N.S. HAHN (Eds). A planície de inundação do alto Rio Paraná: aspectos físicos, biológicos e socioeconômicos. Maringá, EDUEM, 460p.
• BARBIERI, G. & J.R. VERANI. 1987. O fator de condição como indicador do período de desova em Hypostomus aff. plecostomus (Linnaeus, 1758) (Osteichthyes, Loricariidae), na Represa do Monjolinho (São Carlos, SP). Ciência e Cultura, São Paulo, 39: 655-658.
• BARBIERI, G.; A.C. PERET & J.R. VERANI. 1994. Notas sobre adaptação do trato digestivo ao regime alimentar em espécies de peixes da região de São Carlos (SP). I. Quociente intestinal. Revista Brasileira de Biologia, Rio de Janeiro, 54 (1): 63-69.
• ⁶
  BARRETO, B.P.; T.F. RATTON; M.C.P. RICARDO; C.B.M. ALVES; V. VONO; F. VIEIRA; E. RIZZO, & N. BAZZOLI. 1998. Biologia reprodutiva do lambari Astyanax bimaculatus (Pisces, Characidae) no rio Carmo, bacia do rio Grande, São Paulo. Bios, Belo Horizonte, 6 (6): 121-130.
• BAZZOLI, N. 2003. Parâmetros reprodutivos de peixes de interesse comercial na região de Pirapora, p. 291-306. In: H.P. GODINHO & A.L. GODINHO (Eds). Águas, peixes e pescadores do São Francisco das Minas Gerais. Belo Horizonte, CNPq/PADCT, Editora PUC Minas, 468p.
• BAZZOLI, N. & H.P. GODINHO. 1991. Reproductive biology of Acestrorhynchus lacustis (Reinhardt, 1879) (Pisces: Characidae) from Três Marias Reservoir. Zoologischer Anzeiger, Jena, 226: 285-297.
• BAZZOLI, N.; T.L. MESQUITA & G.B. SANTOS. 1998. Análise comparativa da reprodução de Astyanax bimaculatus (Pisces: Characidae) nos reservatórios de Furnas, Marimbondo e Itumbiara. Bios, Belo Horizonte, 6 (6): 99-112.
• BENNEMANN, S.T.; M.L. ORSI & O. SHIBATTA. 1996. Atividade alimentar de espécies de peixes do rio Tibagi, relacionadas com o desenvolvimento de gordura e gônadas. Revista Brasileira de Zoologia, Curitiba, 13 (2): 501-512.
• BRITO, M.F.G. & N. BAZZOLI. 2003. Reproduction of the surubim catfish (Pisces, Pimelodidae) in the São Francisco river, Pirapora Region, Minas Gerais, Brazil. Arquivo Brasileiro de Medicina Veterinária e Zootecnia, Belo Horizonte, 55 (5): 624-633.
• BRITO, R.E.S.; G.B. SANTOS & N. BAZZOLI. 1999. Reprodução de Leporinus friderici (Pisces: Anostomidae) no reservatório de Itumbiara, GO. Bios, Belo Horizonte, 7 (7): 33-40.
• DABÉS, M.B.G.S.; G.B. SANTOS; T.E. RATTON & G.R. MEDEIROS. 2001. Estudo da ictiofauna na barragem do rio Juramento, Juramento/MG - Brasil. Unimontes Científica, Montes Claros, 1 (1): 105-118.
• DELARIVA, R.L.; Agostinho, A.A. 2001. Relationship between morphology and diets of six neotropical loricariids. Journal of Fish Biology, London, 58: 832-847.
• GOMES, J.H.C. & J.R. VERANI. 2003. Alimentação de espécies de peixes no reservatório de Três Marias, p. 195-227. In: H.P. GODINHO & A.L. GODINHO (Eds). Águas, peixes e pescadores do São Francisco das Minas Gerais. Belo Horizonte, CNPq/PADCT, Editora PUC Minas, 468p.
• GURGEL, H.C.B.; L.J.S. VIEIRA & G. BARBIERI. 1995. Análise quantitativa da reprodução de Metynnis cf. roosevelti Eigenmann, 1915 (Characidae, Myleinae), da lagoa Redonda, município de Nízia Floresta, Estado de Rio Grande do Norte, Brasil. Revista Brasileira de Biologia, Rio de Janeiro, 55 (4): 727-736.
• HAHN, N.S.; I.F. ANDRIAN; R. FUGI & V.L.L. ALMEIDA. 1997. Ecologia trófica, p. 209-227. In: A.E.A.M. VAZZOLER; A.A. AGOSTINHO & N.S. HAHN (Eds). A planície de inundação do alto Rio Paraná: aspectos físicos, biológicos e socioeconômicos. Maringá, Editora da Universidade de Maringá, 460p.
• HARTZ, S.M. & G. BARBIERI. 1994. Dinâmica da reprodução de Cyphocharax voga (Hensel, 1869) da lagoa Emboaba, RS, Brasil (Characiformes, Curimatidae). Revista Brasileira de Biologia, Rio de Janeiro, 54 (3): 459-468.
• HOJO, R.E.S.; G.B. SANTOS & N. BAZZOLI. 2004. Reproductive biology of Moenkhausia intermedia (Eigenmann) (Pisces, Characiformes) in Itumbiara Reservoir, Goiás, Brazil. Revista Brasileira de Zoologia, Curitiba, 21 (3): 519-524.
• HTUN-HAN, M. 1978. The reproductive biology of the dab Limanda limanda (L.) in North Sea: gonosomatic index, hepatosomatic index and condiction factor. Journal of Fish Biology, London, 13: 369-378.
• HYSLOP, E.J. 1980. Stomach contents analysis - a review of methods and their application. Journal of Fish Biology, London, 17: 411-429
• LUNARDON-BRANCO, M.J. & J.O. BRANCO. 2003. Alimentação natural de Etropus crossotus Jordan & Gilbert (Teleostei, Pleuronectiformes, Paralichthyidae), na Armação do Itapocoroy, Penha, Santa Catarina, Brasil. Revista Brasileira de Zoologia, Curitiba, 20 (4): 631-635.
• NELSON, J.S. 1994. Fishes of the worlds. New York, John Wiley & Sons, 602p.
• NOGUEIRA, B.P.; N. BAZZOLI; J.E. SANTOS & M.D.M. BARROS. 1997. Biologia reprodutiva do Bryconops cf. affinis = Creatochanes affinis (Gunther, 1864) (Teleostei: Characiformes) na lagoa do Pantaninho, Lagoa da Prata, Minas Gerais. Bios, Belo Horizonte, 5 (5): 43-51.
• PINTO, M.T.C.; L.-W. YU & F.A.R BARBOSA. 2003. Dinâmica mineral na interface terra-água no alto São Francisco, p. 51-69. In: H.P. GODINHO & A.L GODINHO (Eds). Águas, peixes e pescadores do São Francisco das Minas Gerais. Belo Horizonte, CNPq/PADCT, Editora PUC Minas, 468p.
• POMPEU, P.S. 1999. Dieta da pirambeba Serrasalmus brandtii Reinhardt (Teleostei, Characidae) em quatro lagoas marginais do rio São Francisco, Brasil. Revista Brasileira de Zoologia, Curitiba, 16 (Supl. 2.): 19-26.
• QUINTANA, L.; A. SILVA; N. BEROIS & O. MACADAR. 2004. Temperature induces gonadal maturation and effects eletrophysiological sexual maturity indicators in Brachyhypopomus pinnicaudatus from temperate climate. The Journal of Experimental Biology, Cambridge, 207: 1843-1853.
• RICARDO, M.C.P.; G.B. SANTOS; E. RIZZO & N. BAZZOLI. 1997. Aspectos reprodutivos de Leporinus amblyrhynchus Garavello & Brutski, 1987 e Leporinus striatus Kner, 1859 (Pisces: Anostomidae) no reservatório de Furnas, MG. Bios, Belo Horizonte, 5 (5): 29-35.
• RIZZO, E.; Y. SATO; R.M.A. FERREIRA; H. CHIARINI-GARCIA & N. BAZZOLI. 1996. Reproduction of Leporinus reinhardti Lütken, 1874 (Pisces: Anostomidae) from the Três Marias Reservoir, São Francisco River, Minas Gerais, Brazil. Ciência e Cultura, São Paulo, 48 (3): 189-192.
• RODRIGUES, A.M.; J.D. RODRIGUES; A.E. FERREIRA & E.C. CAMPOS. 1989. Aspectos da estrutura populacional do Saguiru Curimata cf. elegans (Steindachner, 1875) (Osteichthyes, Curimatidae) e época de sua reprodução na represa de Bariri, rio Tiête, Estado de São Paulo, Brasil. Boletim do Instituto de Pesca, São Paulo, 16 (1): 57-65.
• SABINO, J. & R.M.C. CASTRO. 1990. Alimentação, período de atividade e distribuição dos peixes de um riacho da floresta Atlântica (sudeste do Brasil). Revista Brasileira de Biologia, Rio de Janeiro, 50 (1): 23-36.
• SATO, Y.; N. FENERICH-VERANI; A.P.O.N. NUNER; H.P. GODINHO & J.R. VERANI. 2003. Padrões reprodutivos de peixes da bacia do São Francisco, p. 229-274. In: H.P. GODINHO & A.L. GODINHO (Eds). Águas, peixes e pescadores do São Francisco das Minas Gerais, Belo Horizonte, CNPq/PADCT, Editora PUC Minas, 468p.
• SCHIFINO, L.C.; C.B. FIALHO & J.R. VERANI. 1998. Reproductive aspects of Cyphocharax voga (Hensel) from Custódias Lagoon, Rio Grande do Sul, Brazil (Characiformes, Curimatidae). Revista Brasileira de Zoologia, Curitiba, 15 (3): 757-766.
• SUZUKI, H.I. & A.A. AGOSTINHO. 1997. Reprodução de peixes do reservatório de Segredo, p. 163-182. In: A.A. AGOSTINHO & L.C GOMES (Eds). Reservatório de Segredo: bases ecológicas para o manejo. Maringá, EDUEM, 387p.
• TAVARES, E.F. & H.P. GODINHO. 1994. Ciclo reprodutivo do peixe piau-gordura (Leporinus piau Fowler, 1941) da Represa de Três Marias, rio São Francisco. Revista Ceres, Viçosa, 41 (233): 28-35.
• THOMÉ, R.G.; N. BAZZOLI; E. RIZZO; G.B. SANTOS & T.F. RATTON. 2005. Reproductive biology of Leporinus taeniatus Lütken (Pisces, Anostomidae) in Juramento Reservoir, São Francisco River basin, Minas Gerais, Southeastern Brazil. Revista Brasileira de Zoologia, Curitiba, 22 (3): 565-570.

1

Corresponding author

Publication Dates

• Publication in this collection
  20 July 2006
• Date of issue
  June 2006

History

• Accepted
  28 Mar 2006
• Received
  16 June 2005