Evident sexual dimorphism in the shape of subadults of astyanax altiparanae (teleostei, characidae)

The fish species known as “lambari” inhabit small streams, lakes, and large rivers throughout the entire tropical environment of the New World; however, there is limited quantitative information regarding its morphological variations. Our investigation was aimed at studying the sexual dimorphism in...

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Autores:
Parés Casanova, Pere Miquel
Cala Delgado, Daniel Leonardo
Salamanca Carreño, Arcesio
Tipo de recurso:
Article of journal
Fecha de publicación:
2022
Institución:
Universidad Cooperativa de Colombia
Repositorio:
Repositorio UCC
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OAI Identifier:
oai:repository.ucc.edu.co:20.500.12494/45819
Acceso en línea:
https://hdl.handle.net/20.500.12494/45819
Palabra clave:
Especies de acuicultura
Estructura animal
Medición corporal
Morfometría geométrica
Plasticidad fenotípica
Aquaculture species
Animal structure
Body measuremen
Geometric morphometrics
Phenotypic plasticity
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openAccess
License
Atribución – No comercial – Sin Derivar
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repository_id_str
dc.title.spa.fl_str_mv Evident sexual dimorphism in the shape of subadults of astyanax altiparanae (teleostei, characidae)
title Evident sexual dimorphism in the shape of subadults of astyanax altiparanae (teleostei, characidae)
spellingShingle Evident sexual dimorphism in the shape of subadults of astyanax altiparanae (teleostei, characidae)
Especies de acuicultura
Estructura animal
Medición corporal
Morfometría geométrica
Plasticidad fenotípica
Aquaculture species
Animal structure
Body measuremen
Geometric morphometrics
Phenotypic plasticity
title_short Evident sexual dimorphism in the shape of subadults of astyanax altiparanae (teleostei, characidae)
title_full Evident sexual dimorphism in the shape of subadults of astyanax altiparanae (teleostei, characidae)
title_fullStr Evident sexual dimorphism in the shape of subadults of astyanax altiparanae (teleostei, characidae)
title_full_unstemmed Evident sexual dimorphism in the shape of subadults of astyanax altiparanae (teleostei, characidae)
title_sort Evident sexual dimorphism in the shape of subadults of astyanax altiparanae (teleostei, characidae)
dc.creator.fl_str_mv Parés Casanova, Pere Miquel
Cala Delgado, Daniel Leonardo
Salamanca Carreño, Arcesio
dc.contributor.author.none.fl_str_mv Parés Casanova, Pere Miquel
Cala Delgado, Daniel Leonardo
Salamanca Carreño, Arcesio
dc.subject.spa.fl_str_mv Especies de acuicultura
Estructura animal
Medición corporal
Morfometría geométrica
Plasticidad fenotípica
topic Especies de acuicultura
Estructura animal
Medición corporal
Morfometría geométrica
Plasticidad fenotípica
Aquaculture species
Animal structure
Body measuremen
Geometric morphometrics
Phenotypic plasticity
dc.subject.other.spa.fl_str_mv Aquaculture species
Animal structure
Body measuremen
Geometric morphometrics
Phenotypic plasticity
description The fish species known as “lambari” inhabit small streams, lakes, and large rivers throughout the entire tropical environment of the New World; however, there is limited quantitative information regarding its morphological variations. Our investigation was aimed at studying the sexual dimorphism in subadults of Astyanax altiparanae, using geometric morphometrics to compare sexes in terms of not only size (height and weight) but also shape. A total of 47 specimens (34 males and 13 females) was randomly collected. Photographs of the lateral plane were obtained without sacrificing the specimens, and eight landmarks were placed in the images. The results showed statistically significant differences between sexes. The length of the snout and thickness of the abdomen and caudal peduncle were greater in females, whereas males presented greater dorsal curvature. Females had tall and robust bodies, whereas males were longer and thinner. The difference in shape is probably associated with the species' defensive or survival strategies. However, whether there are ecological advantages or behavioral aspects in sexual dimorphism is still poorly understood, and further research is required to provide data that can explain the causes.
publishDate 2022
dc.date.accessioned.none.fl_str_mv 2022-07-21T17:36:36Z
dc.date.available.none.fl_str_mv 2022-07-21T17:36:36Z
dc.date.issued.none.fl_str_mv 2022-03-25
dc.type.none.fl_str_mv Artículo
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dc.identifier.bibliographicCitation.spa.fl_str_mv Parés-Casanova, Pere M; Cala, Daniel Leonardo y Salamanca Carreño, Arcesio. 2022. Evident Sexual Dimorphism in the Shape of Subadults of Astyanax altiparanae (Teleostei, Characidae). Int. J. Zoo. Animal Biol. 5(2): 000366
identifier_str_mv 2639-216X
Parés-Casanova, Pere M; Cala, Daniel Leonardo y Salamanca Carreño, Arcesio. 2022. Evident Sexual Dimorphism in the Shape of Subadults of Astyanax altiparanae (Teleostei, Characidae). Int. J. Zoo. Animal Biol. 5(2): 000366
url https://hdl.handle.net/20.500.12494/45819
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dc.relation.references.spa.fl_str_mv 1. Souza MA, Fagundes DC, Leal CG, Pompeu PS (2014) Ecomorphology of Astyanax Species in streams with different substrates. Zoología (Curitiba) 31(1): 42-50. 2. McCoy M, Bolker BM, Osenberg CW, Miner BG, Vonesh JR (2006) Size correction: comparing morphological traits among populations and environments. Oecología 148: 547-554. 3. Galvão GA (2011) Comparação morfométrica de machos e fêmeas de Astyanax bimaculatus (Linnaeus, 1758) capturados em dois açudes da Bacia do Rio Moxotó (PE) sob a influência do Projeto São Francisco. (Graduação em Medicina Veterinária). Universidade Federal do Vale do São Francisco, Campus de Ciências Agrárias. 4. Bookstein FL, Schäfer K, Prossinger H, Seidler H, Fieder M, et al. (1999) Comparing frontal cranial profiles in archaic and modern Homo by morphometric analysis. Anat Rec 257(6): 217-224. 5. Toro IM, Manriquez SG, Suazo GI (2010) Geometric Morphometry and the Study of Biological Forms: From Descriptive Morphology to Quantitative Morphology. International Journal of Morphology 28(4): 977-990. 6. Ruiz CR, Román Valencia C, Herrera MB, Peláez O, Ermakova AA (2011) Variación morfológica de las especies de Astyanax, subgénero Zygogaster (Teleostei, Characidae). Animal Biodiversity and Conservation 34(1): 47-66, 7. Bookstein FL (1992) Morphometric Tools for Landmark Data: Geometry and Biology. Cambridge University Press. 8. Rohlf F, Marcus LF (1993)A revolution in morphometrics. Trends in Ecology & Evolution 8(4): 129-132. 9. Prioli SM, Prioli AJ, Júlio HF, Pavanelli CS, Oliveira AV, et al. (2002) Identification of Astyanax altiparanae (Teleostei, Characidae) in the Iguaçu River, Brazil , Based on Mitochondrial DNA and RAPD Markers. Genet. Mol. Biol 25(4): 421-430. 10. Catilho Almeida RB (2007) Astyanax altiparanae (Pisces, Characiformes) como modelo biológico de espécie de peixe para exploração zootécnica e biomanipulação. Tese Doutorado, Universidade Estadual Paulista - UNESP, Brazil, pp: 1-119. 11. Almeida FS, Santana CA, Lima DM, Andrade LH, Súarez YR, et al. (2016) Discrimination of Astyanax altiparanae (Characiformes, Characidae) populations by applying Fourier transform-infrared photoacoustic spectroscopy in the fish scales. Infrared Physics & Technology 76: 303- 307. 12. Castro JP, Moura MO, Moreira-Filho O, Shibatta OA, Santos MH, (2014) Evidence of incipient speciation in Astyanax scabripinnis species complex (Teleostei: Characidae). Neotropical Ichthyology 12(2): 429-438. 13. Stevanato DJ, Ostrensky A (2018) Ontogenetic development of tetra Astyanax lacustris (Characiformes: Characidae). Neotrop Ichthyol 16(2): 1-10. 14. Rohlf FJ (2015) The tps series of software. Hystrix the Italic Jouyrnal of Mammalogy 26(1): 9-12. 15. Klingenberg CP (2011) MorphoJ: An integrated software package for geometric morphometrics. Mol Ecol Resour 11(2): 353-357. 16. Hammer Ø, Harper DA, Ryan PD (2001) PAST: Paleontological Statisticts Software Package for education and data analysis. Palaeontological Association 4(1): 1-229. 17. Ruíz RI, Cipriani R (2007) Geometric morphometry of Astyanax siape (Pisces:Characidae). Dahlia (Rev. Asoc. Colomb. Ictiol.) 9: 63-75.
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spelling Parés Casanova, Pere MiquelCala Delgado, Daniel Leonardo Salamanca Carreño, Arcesio5(2)2022-07-21T17:36:36Z2022-07-21T17:36:36Z2022-03-252639-216Xhttps://hdl.handle.net/20.500.12494/45819Parés-Casanova, Pere M; Cala, Daniel Leonardo y Salamanca Carreño, Arcesio. 2022. Evident Sexual Dimorphism in the Shape of Subadults of Astyanax altiparanae (Teleostei, Characidae). Int. J. Zoo. Animal Biol. 5(2): 000366The fish species known as “lambari” inhabit small streams, lakes, and large rivers throughout the entire tropical environment of the New World; however, there is limited quantitative information regarding its morphological variations. Our investigation was aimed at studying the sexual dimorphism in subadults of Astyanax altiparanae, using geometric morphometrics to compare sexes in terms of not only size (height and weight) but also shape. A total of 47 specimens (34 males and 13 females) was randomly collected. Photographs of the lateral plane were obtained without sacrificing the specimens, and eight landmarks were placed in the images. The results showed statistically significant differences between sexes. The length of the snout and thickness of the abdomen and caudal peduncle were greater in females, whereas males presented greater dorsal curvature. Females had tall and robust bodies, whereas males were longer and thinner. The difference in shape is probably associated with the species' defensive or survival strategies. However, whether there are ecological advantages or behavioral aspects in sexual dimorphism is still poorly understood, and further research is required to provide data that can explain the causes.https://scienti.minciencias.gov.co/cvlac/visualizador/generarCurriculoCv.do?cod_rh=0001022903https://orcid.org/0000-0002-5416-5906https://orcid.org/0000-0003-1440-6418https://orcid.org/0000-0003-4639-5952https://scienti.minciencias.gov.co/gruplac/jsp/visualiza/visualizagr.jsp?nro=00000000009387pmpares@gencat.catdaniel.cala@campusucc.edu.coasaca_65@yahoo.esarcesio.salamanca@campusucc.edu.cohttps://scholar.google.com/citations?hl=es&user=EqGLQZUAAAAJ1-5 p. Facultad de Medicina Veterinaria y Zootecnia. Universidad Cooperativa de ColombiaMedicina veterinaria y zootecniaVillavicenciohttps://medwinpublishers.com/IZAB/evident-sexual-dimorphism-in-the-shape-of-subadults-of-astyanax-altiparanae-teleostei-characidae.pdfhttps://medwinpublishers.com/IZAB/volume.php?volumeId=434&issueId=13421. Souza MA, Fagundes DC, Leal CG, Pompeu PS (2014) Ecomorphology of Astyanax Species in streams with different substrates. Zoología (Curitiba) 31(1): 42-50. 2. McCoy M, Bolker BM, Osenberg CW, Miner BG, Vonesh JR (2006) Size correction: comparing morphological traits among populations and environments. Oecología 148: 547-554. 3. Galvão GA (2011) Comparação morfométrica de machos e fêmeas de Astyanax bimaculatus (Linnaeus, 1758) capturados em dois açudes da Bacia do Rio Moxotó (PE) sob a influência do Projeto São Francisco. (Graduação em Medicina Veterinária). Universidade Federal do Vale do São Francisco, Campus de Ciências Agrárias. 4. Bookstein FL, Schäfer K, Prossinger H, Seidler H, Fieder M, et al. (1999) Comparing frontal cranial profiles in archaic and modern Homo by morphometric analysis. Anat Rec 257(6): 217-224. 5. Toro IM, Manriquez SG, Suazo GI (2010) Geometric Morphometry and the Study of Biological Forms: From Descriptive Morphology to Quantitative Morphology. International Journal of Morphology 28(4): 977-990. 6. Ruiz CR, Román Valencia C, Herrera MB, Peláez O, Ermakova AA (2011) Variación morfológica de las especies de Astyanax, subgénero Zygogaster (Teleostei, Characidae). Animal Biodiversity and Conservation 34(1): 47-66, 7. Bookstein FL (1992) Morphometric Tools for Landmark Data: Geometry and Biology. Cambridge University Press. 8. Rohlf F, Marcus LF (1993)A revolution in morphometrics. Trends in Ecology & Evolution 8(4): 129-132. 9. Prioli SM, Prioli AJ, Júlio HF, Pavanelli CS, Oliveira AV, et al. (2002) Identification of Astyanax altiparanae (Teleostei, Characidae) in the Iguaçu River, Brazil , Based on Mitochondrial DNA and RAPD Markers. Genet. Mol. Biol 25(4): 421-430. 10. Catilho Almeida RB (2007) Astyanax altiparanae (Pisces, Characiformes) como modelo biológico de espécie de peixe para exploração zootécnica e biomanipulação. Tese Doutorado, Universidade Estadual Paulista - UNESP, Brazil, pp: 1-119. 11. Almeida FS, Santana CA, Lima DM, Andrade LH, Súarez YR, et al. (2016) Discrimination of Astyanax altiparanae (Characiformes, Characidae) populations by applying Fourier transform-infrared photoacoustic spectroscopy in the fish scales. Infrared Physics & Technology 76: 303- 307. 12. Castro JP, Moura MO, Moreira-Filho O, Shibatta OA, Santos MH, (2014) Evidence of incipient speciation in Astyanax scabripinnis species complex (Teleostei: Characidae). Neotropical Ichthyology 12(2): 429-438. 13. Stevanato DJ, Ostrensky A (2018) Ontogenetic development of tetra Astyanax lacustris (Characiformes: Characidae). Neotrop Ichthyol 16(2): 1-10. 14. Rohlf FJ (2015) The tps series of software. Hystrix the Italic Jouyrnal of Mammalogy 26(1): 9-12. 15. Klingenberg CP (2011) MorphoJ: An integrated software package for geometric morphometrics. Mol Ecol Resour 11(2): 353-357. 16. Hammer Ø, Harper DA, Ryan PD (2001) PAST: Paleontological Statisticts Software Package for education and data analysis. Palaeontological Association 4(1): 1-229. 17. Ruíz RI, Cipriani R (2007) Geometric morphometry of Astyanax siape (Pisces:Characidae). Dahlia (Rev. Asoc. Colomb. 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