Acta Limnologica Brasiliensia
http://www.alb.periodikos.com.br/article/doi/10.1590/S2179-975X7725
Acta Limnologica Brasiliensia
Original Article

Reproductive biology traits of two invasive fish species in Rio Doce State Park, Minas Gerais, Brazil

Traços da biologia reprodutiva de duas espécies invasoras de peixe no Parque Estadual do Rio Doce, MG, Brasil

Ludmila Silva Brighenti; Gabriel Rossi Diniz Costa; Thaís Paula de Araújo; Lorena Torres Oporto; Hélio Batista dos Santos; Ralph Gruppi Thomé

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Abstract

Aim: This study aims to analyze the reproductive biology of two invasive fish species, tucunaré (Cichla kelberi) and red piranha (Pygocentrus nattereri), introduced into the middle Rio Doce Lake system (southeastern Brazil).

Methods: Quarterly samplings were carried out from 2018 to 2019 using gillnets and casting nets. For each individual, biometric data were recorded and the gonadal maturation stage was determined by macroscopic and histological analyses. Sex ratio, length–weight relationship, gonadosomatic index, and reproductive stages were analyzed to characterize reproductive patterns.

Results: A total of 132 red piranhas and 33 tucunarés were captured. Both species presented males and females at all reproductive stages throughout the year indicating asynchronous spawning and successful reproduction in the invaded environment. A higher frequency of spawned females occurred in July and September for tucunaré, corresponding to the dry season, and between December and March for red piranha, coinciding with the rainy season. The species exhibited distinct growth patterns: positive allometric growth for the tucunaré and negative for the red piranha. Histological analyses revealed typical gonadal development patterns for freshwater fish, with traits associated with parental care behavior.

Conclusions: The tucunaré showed reproductive activity toward the dry season, contrasting with the well-defined rainy season reproductive peak observed for the red piranha. This suggests a potential temporal partitioning of reproductive niches. The results reinforce that both species are successfully reproducing under local environmental conditions and highlight the ecological risks associated with their introduction into protected Atlantic Forest ecosystems.

Keywords

biological invasions; reproduction; Cichla kelberi; Pygocentrus nattereri; non-native species

Resumo

Objetivo: Este estudo teve como objetivo analisar a biologia reprodutiva de duas espécies de peixes invasoras, o tucunaré (Cichla kelberi) e a piranha-vermelha (Pygocentrus nattereri), introduzidas no sistema lacustre do Médio Rio Doce, sudeste do Brasil.

Métodos: Amostragens trimestrais foram realizadas entre 2018 e 2019 com redes de emalhar e de arrasto. Para cada indivíduo, registraram-se dados biométricos e o estágio de maturação gonadal foi determinado por análises macroscópicas e histológicas. A proporção sexual, a relação comprimento-peso, o índice gonadossomático e os estágios reprodutivos foram analisados para caracterizar os padrões reprodutivos.

Resultados: Foram capturados 132 indivíduos de piranha-vermelha e 33 de tucunaré. Ambas as espécies apresentaram machos e fêmeas em todos os estágios reprodutivos ao longo do ano, indicando desova assíncrona e reprodução bem-sucedida no ambiente invadido. Maior frequência de fêmeas desovadas ocorreu em julho e setembro para o tucunaré (não significativa) e entre dezembro e março para a piranha-vermelha (significativa). As espécies exibiram padrões de crescimento distintos, com alometria positiva para o tucunaré e negativa para a piranha-vermelha. Análises histológicas revelaram padrões típicos de desenvolvimento gonadal em peixes de água doce, com características associadas ao cuidado parental.

Conclusões: O tucunaré apresenta tendência reprodutiva associada à estação seca, enquanto a piranha-vermelha apresenta pico bem definido na estação chuvosa, sugerindo partição temporal dos nichos reprodutivos. Os resultados indicam que ambas as espécies se reproduzem com sucesso sob as condições locais e destacam riscos ecológicos associados à sua introdução em ecossistemas protegidos da Mata Atlântica, com potenciais impactos negativos adicionais relevantes.

Palavras-chave

invasões biológicas; reprodução; Cichla kelberi; Pygocentrus nattereri; espécies não-nativas

Referencias

Andrade, G.D.S., & Pelicice, F.M., 2022. Coexistence of endemic peacock basses (Cichla) in a Neotropical reservoir (Cichlidae: cichliformes). Neotrop. Ichthyol., 20(3), e220039. https://doi.org/10.1590/1982-0224-2022-0039.

Araújo, T.P., Brighenti, L.S., Dolabela, B.M., Ribeiro, S.P., dos Santos, H.B., & Thomé, R.G., 2022. Can the introduction of non-native fish induce variation in life-history traits of a native species in a neotropical lake? Mar. Freshw. Res., 73(5), 651-661. https://doi.org/10.1071/MF21138.

Azour, F., van Deurs, M., Behrens, J., Carl, H., Hüssy, K., Greisen, K., Ebert, R., & Møller, P.R., 2015. Invasion rate and population characteristics of the round goby Neogobius melanostomus: effects of density and invasion history. Aquat. Biol., 24(1), 41-52. https://doi.org/10.3354/ab00634.

Bezerra-Neto, J.F., & Pinto-Coelho, R.M., 2008. Morphometric study of Lake Dom Helvécio, Parque Estadual do Rio Doce (PERD), Minas Gerais, Brazil: A re-evaluation. Acta Limnol. Bras., 20(2), 117-130.

Bezerra-Neto, J.F., Brighenti, L.S., & Pinto-Coelho, R.M., 2010. A new morphometric study of Carioca Lake, Parque Estadual do Rio Doce (PERD), Minas Gerais State, Brazil. Acta Sci. Biol. Sci., 32(1), 49-54. https://doi.org/10.4025/actascibiolsci.v32i1.4990.

Blackburn, T.M., Pyšek, P., Bacher, S., Carlton, J.T., Duncan, R.P., Jarošík, V., Wilson, J.R.U., & Richardson, D.M., 2011. A proposed unified framework for biological invasions. Trends Ecol. Evol., 26(7), 333-339. PMid:21601306. https://doi.org/10.1016/j.tree.2011.03.023.

Bueno, M.L., Magalhães, A.L.B., Andrade Neto, F.R., Alves, C.B.M., Rosa, D.M., Junqueira, N.T., Pessali, T.C., Pompeu, P.S., & Zenni, R.D., 2021. Alien fish fauna of southeastern Brazil: species status, introduction pathways, distribution and impacts. Biol. Invasions 23(10), 3021-3034. https://doi.org/10.1007/s10530-021-02564-x.

Carvajal-Vallejos, F., Gallo-Cardozo, F., Careaga, M., & Campero, M., 2025. Weight–length relationships of piranhas Serrasalmus in Bolivia: relationships to molecular divergence and maximum size. Ecol. Evol., 15(1), e70970. PMid:41069873. https://doi.org/10.1002/ece3.70970.

Carvalho, I.F.S., Cantanhêde, L.G., Diniz, A.L.C., Carvalho-Neta, R.N.F., & Almeida, Z.S., 2021. Reproductive biology of seven fish species of commercial interest. Neotrop. Ichthyol., 19(1), e200067. https://doi.org/10.1590/1982-0224-2020-0067.

Carvalho, T., De Almeida Ferreira, E., Pelicice, F.M., & Fernandes, R., 2020. Comparative functional responses predict the predatory impact of the highly invasive fish Cichla kelberi. Hydrobiologia 848(9), 2203-2211. https://doi.org/10.1007/s10750-020-04440-6.

Chellappa, S., Câmara, M., & Chellappa, N., 2003. Ecology of Cichla monoculus (Osteichthyes: Cichlidae) from a reservoir in the semi-arid region of Brazil. Hydrobiologia 504(1-3), 267-273. https://doi.org/10.1023/B:HYDR.0000008526.83477.2f.

DeLorenzo, L., Mathews, D., Brandon, A., Joglekar, M., Baez, A., Moore, E., Ciccotto, P., Roberts, N., Roberts, R., & Powder, K.E., 2023. Genetic basis of ecologically relevant body shape variation among four genera of cichlid fishes. Mol. Ecol., 32(14), 3975-3988. PMid:37161914. https://doi.org/10.1111/mec.16977.

Dias, J.O., Sant’Anna, I.R.A., Bezerra Neto, E.F.S., Sousa, R.G.C., & Dantas Filho, J.A.S., 2024. Population parameters of the red-bellied piranha Pygocentrus nattereri. Bol. Inst. Pesca 50, e853. https://doi.org/10.20950/1678-2305/bip.2024.50.e853.

Dikou, A., 2022. Weight–length relationship in fish populations reflects environmental regulation on growth. Hydrobiologia 850(2), 335-346. https://doi.org/10.1007/s10750-022-05072-8.

Dudgeon, D., & Strayer, D.L., 2024. Bending the curve of global freshwater biodiversity loss. Biol. Rev. Camb. Philos. Soc., 100(1), 205-226. PMid:39221642. https://doi.org/10.1111/brv.13137.

Duponchelle, F., Lino, F., Hubert, N., Panfili, J., Renno, J.F., Baras, E., Torrico, J.P., Dugué, R., & Nuñez, J., 2007. Environment-related life-history trait variations of Pygocentrus nattereri. J. Fish Biol., 71(4), 1113-1134. https://doi.org/10.1111/j.1095-8649.2007.01583.x.

Feldman, A.T., & Wolfe, D., 2014. Tissue processing and hematoxylin and eosin staining. Methods Mol. Biol., 1180, 31-43. PMid:25015141. https://doi.org/10.1007/978-1-4939-1050-2_3.

Fennell, J.M., Rosenthal, W.C., Wagner, C., Burckhardt, J., & Walters, A.W., 2022. Temporal segregation in spawning between native Yellowstone cutthroat trout and introduced rainbow trout. Ecol. Freshwat. Fish 32(1), 94-106. https://doi.org/10.1111/eff.12672.

Fragoso-Moura, E.N., Oporto, L.T., Maia-Barbosa, P.M., & Barbosa, F.A.R., 2016. Loss of biodiversity in a Neotropical lake: response of a planktonic community to fish introduction. Braz. J. Biol., 76(1), 18-27. PMid:26909619. https://doi.org/10.1590/1519-6984.07914.

Fráguas, P.S., de Carvalho, D.R., de Castro, C.C., Ferreira, F.F., Dergam, J.A., Sperber, C.F., & Pompeu, P.S., 2025. Temporal stability in fish assemblage isotopic niches. Environ. Biol. Fishes 108(5), 835-852. https://doi.org/10.1007/s10641-025-01688-6.

Fryxell, D.C., Arnett, H.A., Apgar, T.M., Kinnison, M.T., & Palkovacs, E.P., 2015. Sex ratio variation shapes the ecological effects of a globally introduced freshwater fish. Proc. Biol. Sci., 282(1817), 20151970. PMid:26490793. https://doi.org/10.1098/rspb.2015.1970.

Gaspar, M.R.C., Agostinho, A.A., Catelani, P.A., Fernandes, R., Franco, A.C.S., Novaes, J.L.C., Peretti, D., Petry, A.C., & Pelicice, F.M., 2025. Phenotypic and behavioral variation as invasion mechanisms in freshwater fishes. Hydrobiologia 852(8), 2133-2147. https://doi.org/10.1007/s10750-024-05663-7.

Giarrizzo, T., de Sena Oliveira, R.R., Costa Andrade, M., Pedrosa Gonçalves, A., Barbosa, T.A.P., Martins, A.R., & Melo de Sousa, L., 2015. Length–weight relationships for 102 fish species from Xingu River, Brazilian Amazon. J. Appl. Ichthyology 31(2), 415-424. https://doi.org/10.1111/jai.12677.

Google Maps, 2026. Google Maps: imagem de satélite da área de estudo [Lagoa Carioca]. Mountain View: Google [online]. Retrieved in 2026, June 4, from https://www.google.com/maps

Gross, M.R., 2005. The evolution of parental care. Q. Rev. Biol., 80(1), 37-45. PMid:15884734. https://doi.org/10.1086/431023.

Guedes, G.H.S., Gomes, I.D., Nascimento, A.A., Aguiar, F.S., & Araújo, F.G., 2021. Reproductive strategy of Cichla kelberi (Perciformes: Cichlidae) in a Neotropical reservoir. J. Fish Biol., 98(3), 743-755. PMid:33206375. https://doi.org/10.1111/jfb.14618.

Jepsen, D.B., Winemiller, K.O., Taphorn, D.C., & Olarte, D.R., 1999. Age structure and growth of Cichla species from a Neotropical blackwater river. J. Fish Biol., 55(2), 433-450. https://doi.org/10.1111/j.1095-8649.1999.tb00689.x.

Langerhans, R.B., 2009. Trade-off between swimming modes in mosquitofish (Gambusia affinis). J. Evol. Biol., 22(5), 1057-1068. PMid:21462405. https://doi.org/10.1111/j.1420-9101.2009.01716.x.

Latini, A.O., & Petrere Junior, M., 2004. Reduction of native fish fauna in four natural lakes of Southeastern Brazil which were introduced with exotic species. Fish. Manag. Ecol., 11(2), 71-79. https://doi.org/10.1046/j.1365-2400.2003.00372.x.

Le Cren, E.D., 1951. The length-weight relationship and seasonal cycle in gonad weight and condition in the perch (Perca fluviatilis). J. Anim. Ecol., 20(2), 201-219. https://doi.org/10.2307/1540.

Lowe, A., Kolmann, M., & Paig-Tran, E.W.M., 2023. How to survive a piranha attack: functional morphology of armor in armored catfish (Callichthyidae). Integr. Org. Biol., 5(1), obad032. PMid:37818205. https://doi.org/10.1093/iob/obad032.

Lowerre‐Barbieri, S.K., Ganias, K., Saborido‐Rey, F., Murua, H., & Hunter, J.R., 2011. Reproductive timing in marine fishes: variability, temporal scales, and methods. Mar. Coast. Fish. 3(1), 71-91. https://doi.org/10.1080/19425120.2011.556932.

Mann, H.B., & Whitney, D.R., 1947. On a test of whether one of two random variables is stochastically larger than the other. Ann. Math. Stat., 18(1), 50-60. https://doi.org/10.1214/aoms/1177730491.

Marto, V.C.O., Akama, A., & Pelicice, F.M., 2015. Feeding and reproductive ecology of Pygocentrus nattereri Kner, 1858 in a Neotropical reservoir. Neotrop. Ichthyol., 13(3), 625-636. https://doi.org/10.1590/1982-0224-20140165.

Muñoz, H., Van Damme, P.A., & Duponchelle, F., 2006. Breeding behaviour of Pygocentrus nattereri, Serrasalmus spilopleura and S. humeralis (Characiformes: Characidae) in the Bolivian Amazon. J. Fish Biol., 69(4), 1018-1030. https://doi.org/10.1111/j.1095-8649.2006.01177.x.

Nakayama, S., Rose, K.A., & Fuiman, L.A., 2011. Batch spawning in a coastal fish: implications for reproductive success. Mar. Ecol. Prog. Ser., 441, 213-223. https://doi.org/10.3354/meps09382.

Normando, F.T., Arantes, F.P., Luz, R.K., Thomé, R.G., Rizzo, E., Sato, Y., & Bazzoli, N., 2009. Reproduction and fecundity of the piranha Pygocentrus nattereri Kner, 1858 in the São Francisco River, Southeastern Brazil. J. Appl. Ichthyology 25(3), 299-305. https://doi.org/10.1111/j.1439-0426.2008.01174.x.

Pelicice, F.M., & Agostinho, A.A., 2009. Fish fauna destruction after the introduction of a non-native apex predator (Cichla kelberi) in a Neotropical reservoir. Biol. Invasions 11(8), 1789-1801. https://doi.org/10.1007/s10530-008-9358-3.

MapBiomas, 2026. Coleção 10.1 da Série Anual de Mapas de Cobertura e Uso da Terra do Brasil. Mountain View: Google Earth Engine [online]. Retrieved in 2026, June 4, from https://plataforma.brasil.mapbiomas.org/

Queiroz, H.L., Sobanski, M.B., & Magurran, A.E., 2010. Reproductive strategies of piranhas (Serrasalmus spp.) in the Mamirauá Reserve, Brazilian Amazon. Environ. Biol. Fish., 89(1), 11-19. https://doi.org/10.1007/s10641-010-9658-1.

R Core Team, 2024. R: A language and environment for statistical computing [online]. Vienna: R Foundation for Statistical Computing. Retrieved in 2026, June 4, from https://www.R-project.org/

Reid, A.J., Carlson, A.K., Creed, I.F., Eliason, E.J., Gell, P.A., Johnson, P.T.J., Kidd, K.A., MacCormack, T.J., Olden, J.D., Ormerod, S.J., Smol, J.P., Taylor, W.W., Tockner, K., Vermaire, J.C., Dudgeon, D., & Cooke, S.J., 2018. Emerging threats and persistent conservation challenges for freshwater biodiversity. Biol. Rev. Camb. Philos. Soc., 94(3), 849-873. PMid:30467930. https://doi.org/10.1111/brv.12480.

Rizzo, E., & Bazzoli, N., 2020. Reproduction and embryogenesis. In: Baldisserotto, B., Urbinati, E.C., & Cyrino, J.E.P., eds. Biology and physiology of freshwater neotropical fish. Amsterdam: Academic Press, 287-313. https://doi.org/10.1016/B978-0-12-815872-2.00013-0.

Russo, T., Costa, C., & Cataudella, S., 2007. Correspondence between shape and feeding habit in Neotropical cichlids. J. Fish Biol., 71(3), 629-656. https://doi.org/10.1111/j.1095-8649.2007.01528.x.

Santos, A.C.A., Santos, L.S., & Araújo, F.G., 2010. Digestive tract morphology and feeding habits of Cichla kelberi. Rev. Biol. Trop., 58(4), 1245-1255. https://doi.org/10.15517/rbt.v58i4.5411.

Sharpe, D., 2015. Chi-square test is statistically significant: now what? Pract. Assess. Res. Eval., 20(1), 8. https://doi.org/10.7275/tbfa-x148.

Souza, C.S., Rodrigues-Filho, C.A.O., Barbosa, F.A.R., & Leitão, R.P., 2021. Drastic reduction of the functional diversity of native ichthyofauna. Neotrop. Ichthyol., 19(4), e210033. https://doi.org/10.1590/1982-0224-2021-0033.

Souza, J.E.D., Fragoso-Moura, E.N., Fenerich-Verani, N., Rocha, O., & Verani, J.R., 2008. Population structure and reproductive biology of Cichla kelberi (Perciformes, Cichlidae) in Lobo Reservoir, Brazil. Neotrop. Ichthyol., 6(2), 201-210. https://doi.org/10.1590/S1679-62252008000200007.

Suzuki, H.I., Agostinho, A.A., & Winemiller, K.O., 2000. Oocyte morphology and reproductive strategy in Neotropical freshwater fishes. J. Fish Biol., 57(3), 791-807. https://doi.org/10.1111/j.1095-8649.2000.tb00275.x.

Tozato, H.C., 2017. Gestão de áreas protegidas. Rev. Gest. Polit. Publicas 7(2), 147-169. https://doi.org/10.11606/issn.2237-1095.v7p147-169.

Tundisi, J.G., & Saijo, Y., 1997. Limnological studies on the Rio Doce valley lakes, Brazil. São Carlos: Brazilian Academy of Sciences, University of São Paulo.

Vicentin, W., dos Santos Costa, F.E., & Súarez, Y.R., 2013. Population ecology of piranha Pygocentrus nattereri (Characiformes, Characidae) in the Negro River basin, Pantanal, Brazil. Environ. Biol. Fishes 96(1), 57-66. https://doi.org/10.1007/s10641-012-0022-5.

Zeyl, J.N., Love, O.P., & Higgs, D.M., 2014. Gonadosomatic index evaluation in freshwater fishes. J. Great Lakes Res., 40(1), 164-171. https://doi.org/10.1016/j.jglr.2013.12.004.
 


Submitted date:
03/11/2025

Accepted date:
04/08/2026

Publication date:
04/09/2026

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