Modal and empirical lengths at sexual maturity for six deep-sea species in Ecuadorian oceanic waters

Authors

  • René Zambrano Instituto Superior Tecnológico “Luis Arboleda Martínez” Extensión Jaramijó, 132150 - Jaramijó, Ecuador - Manejo y Conservación de Recursos Naturales S. A. S., Alborada etapa XIII, 090509 - Guayaquil, Ecuador
  • Dialhy Coello Manejo y Conservación de Recursos Naturales S. A. S., Alborada etapa XIII, 090509 - Guayaquil, Ecuador - Departamento de Ciencias del Mar, Facultad de Ciencias Naturales, Universidad de Guayaquil, 090601 - Guayaquil, Ecuador
  • Marco Herrera Instituto Público de Investigación de Acuicultura y Pesca, 090308 - Guayaquil, Ecuador

DOI:

https://doi.org/10.47193/mafis.3722024010501

Keywords:

Dissostichus eleginoides, experimental fishery, kernel density, longline, mature individuals

Abstract

The objective of the present work was to establish modal lengths, empirical lengths at sexual maturity, and proportions of mature individuals of six deep-sea species from the bycatch of the experimental fishery for Patagonian toothfish (Dissostichus eleginoides). Fishing was conducted in Ecuadorian oceanic waters by only one vessel, between 2017 and 2021. Modal lengths were identified using frequency distributions. The length at sexual maturity (Lm) was estimated using the empirical equation: Ln Lm = -0.1189 + 0.9157 * Ln (Lmax). Modal lengths presented a little annual increment in Antimora rostrata and Coryphaenoides armatus while the values decreased for Centroscymnus owstonii, C. delsolari, and Hydrolagus melanophasma. Interannual lengths were similar for Etmopterus granulosus. Modal lengths were higher than the sexual maturity length for H. melanophasma, C. delsolari, C. owstonii and A. rostrata. Furthermore, Coryphaenoides armatus showed a similar value and E. granulosus a lower modal length. Empirical length at sexual maturity was between 56.35 and 66.26 cm TL for all species except for H. melanophasma, which was 100.53 cm TL. Antimora rostrata and C. armatus presented an increment of mature individuals while the annual percentage decreased for H. melanophasma, C. owstonii, and C. delsolari. Etmopterus granulosus showed a lower proportion of mature individuals.

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Author Biographies

René Zambrano, Instituto Superior Tecnológico “Luis Arboleda Martínez” Extensión Jaramijó, 132150 - Jaramijó, Ecuador - Manejo y Conservación de Recursos Naturales S. A. S., Alborada etapa XIII, 090509 - Guayaquil, Ecuador

Dialhy Coello, Manejo y Conservación de Recursos Naturales S. A. S., Alborada etapa XIII, 090509 - Guayaquil, Ecuador - Departamento de Ciencias del Mar, Facultad de Ciencias Naturales, Universidad de Guayaquil, 090601 - Guayaquil, Ecuador

References

Alfaro-Shigueto J, Ebert DA, Guidino C, Velez-Zuazo X, Romero J, Mangel JC. 2022. Deep-sea Chondrichthyans associated with the Patagonian toothfish Dissostichus eleginoides fishery off the coast of Peru. Rev Biol Mar Oceanogr. 57: 1-6. DOI: https://doi.org/10.22370/rbmo.2022.57.especial.3415

Aramayo V. 2016. Breve síntesis sobre el recurso bacalao de profundidad Dissostichus eleginoides en Perú. Rev Biol Mar Oceanogr. 51 (2): 229-239. DOI: https://doi.org/10.4067/s0718-19572016000200002

Araya JF, Reyes P, Hüne M. 2020. On the presence of the Eastern Pacific black ghostshark Hydrolagus melanophasma (Chondrichthyes: Chimaeridae) in northern Chile, with notes on its distribution in the eastern Pacific. Thalassas. 36 (2): 565-572. DOI: https://doi.org/10.1007/s41208-020-00209-9

Baldé BS, Fall M, Kantoussan J, Sow FN, Diouf M, Brehmer P. 2019. Fish-length based indicators for improved management of the sardinella fisheries in Senegal. Reg Stud Mar Sci. 31: 100801. DOI: https://doi.org/10.1016/j.rsma.2019.100801

Bergstad OA, Hunter RH, Cousins NJ, Bailey DM, Jørgensen T. 2021. Notes on age determination, size and age structure, longevity and growth of co-occurring macrourid fishes. J Fish Biol. 99 (3): 1032-1043. DOI: https://doi.org/10.1111/jfb.14801

Binohlan C, Froese R. 2009. Empirical equations for estimating maximum length from length at first maturity. J Appl Ichthyol. 25 (5): 611-613. DOI: https://doi.org/10.1111/j.1439-0426.2009.01317.x

Bustamante C, Flores H, Concha-Pérez Y, Vargas-Caro C, Lamilla J, Bennett M. 2012. First record of Hydrolagus melanophasa James, Ebert, Long & Didier, 2009 (Chondrichthyes, Chimaeriformes, Holocephali) from the southeastern Pacific Ocean. Lat Am J Aquat Res. 40 (1): 236-242. DOI: https://doi.org/10.3856/vol40-issue1-fulltext-23

Collins MA, Brickle P, Brown J, Belchier M. 2010. The Patagonian toothfish. Biology, ecology and fishery. In: Lesser M, editor. Advances in Marine Biology. Vol. 58. Burlington: Academic Press. p. 227-300.

Harford WJ, Amoroso R, Bell RJ, Caillaux M, Cope JM, Dougherty D, Dowling NA, Hurd F, Lomonico S, Nowlis J, et al. 2021. Multi-Indicator harvest strategies for data-limited fisheries: a practitioner guide to learning and design. Front Mar Sci. 8: 757877. DOI: https://doi.org/10.3389/fmars.2021.757877

Irvine SB, Laurenson LJB, Stevens JD. 2002. Hermaphroditism in the southern lantern shark, Etmopterus granulosus. In: International Congress on the Biology of Fish. Vancuver: University of British Columbia. p. 49-54.

Iwamoto T, Stein DL. 1974. A systematic review of the rattail fishes (Macrouridae: Gadiformes) from Oregon and adjacent waters. Occas Pap Calif Acad Sci. 111: 1-79. DOI: https://doi.org/10.5962/bhl.part.15932

Lappalainen A, Saks L, Šuštar M, Heikinheimo O, Jürgens K, Kokkonen E, Kurkilahti M, Verliin A, Vetemaa M. 2016. Length at maturity as a potential indicator of fishing pressure effects on coastal pikeperch (Sander lucioperca) stocks in the northern Baltic Sea. Fish Res. 174: 47-57. DOI: https://doi.org/10.1016/j.fishres.2015.08.013

Magnússon JV. 2001. Distribution and some other biological parameters of two morid species Lepidion eques (Gunther, 1887) and Antimora rostrata (Gunther, 1878) in Icelandic waters. Fish Res. 51: 267-281.

Middleton RW, Musick JA. 1986. The abundance and distribution of the Family Macrouridae (Pisces, Gadiformes) in the Norfolk Canyon Area. Fish Bull. 84 (1): 35-62. https://scholarworks.wm.edu/vimsarticles/623.

Palacios J, Barriga E, Salazar C, Rodriguez A, Romero M. 2009. Aspectos de la biologia de Coryphaenoides delsolari Chirichigno & Iwamoto, 1977 frente a la zona norte del Peru. Lat Am J Aquat Res. 37 (3): 455-462. DOI: https://doi.org/10.3856/vol37-issue3-fulltext-14

Rosenblatt M. 1956. Remarks on some nonparametric estimates of a density function. Ann Math Statist. 27 (3): 832-837. DOI: https://doi.org/10.1214/aoms/1177728190

Salgado-Ugarte IH. 2002. Suavización no paramétrica para análisis de datos. Ciudad de México: Facultad de Estudios Superiores Zaragoza, Universidad Nacional Autónoma de México.

Salgado-Ugarte IH, Saito-Quezada VM. 2020. Métodos cuantitativos computarizados para biología pesquera. Ciudad de México: Facultad de Estudios Superiores Zaragoza, Universidad Nacional Autónoma de México. 487 p.

Scott DW. 1992. Multivariate density estimation: theory, practice, and visualization. New York: John Wiley and Sons.

Sepa P, Coello D, Herrera M, Zambrano R. 2022. Length-weight relationship of four deep-sea chondrichthyans (Elasmobranchii & Holocephali) in Ecuadorian oceanic waters. Egypt J Aquat Res. 48: 397-399. DOI: https://doi.org/10.1016/j.ejar.2021.10.003

Shin YJ, Rochet MJ, Jennings S, Field JG, Gislason H. 2005. Using size-based indicators to evaluate the ecosystem effects of fishing. ICES J Mar Sci. 62 (3): 384-396. DOI: https://doi.org/10.1016/j.icesjms.2005.01.004

Silverman BW. 1986. Density estimation for statistics and data analysis. Monographs on Statistics and Applied Probability. Vol. 26. London: Chapman and Hall/CRC. 186 p.

Wetherbee BM. 1996. Distribution and reproduction of the southern lantern shark from New Zealand. J Fish Biol. 49 (6): 1186-1196. DOI: https://doi.org/10.1111/j.1095-8649.1996.tb01788.x

Yano K, Tanaka S. 1988. Size at maturity, reproductive cycle, fecundity, and depth segregation of the deep sea squaloid sharks Centroscymnus owstoni and C. coelolepis in Suruga Bay, Japan. Nippon Suisan Gakkaishi. 54 (2): 167-174.

Yeh J, Drazen JC. 2011. Baited-camera observations of deep-sea megafaunal scavenger ecology on the California slope. Mar Ecol Prog Ser. 424: 145-156. DOI: https://doi.org/10.3354/meps08972

Zambrano R, Galindo-Cortes G. 2019. Re-description of the growth pattern of four decapod species by information theory. Invertebr Reprod Dev. 63 (1): 51-59. DOI: https://doi.org/10.1080/07924259.2018.1532929

Zambrano R, Galindo-Cortes G, Aragón-Noriega AE. 2018. Comparison of growth pattern of male Ucides occidentalis (Ortmann, 1897) (Brachyura: Ocypodidae) based on a combination of commercial catches and non-commercial data. J Crustac Biol. 38 (4): 429-434. DOI: https://doi.org/10.1093/jcbiol/rux105

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Published

2023-11-16

How to Cite

Zambrano, R., Coello, D. and Herrera, M. (2023) “Modal and empirical lengths at sexual maturity for six deep-sea species in Ecuadorian oceanic waters”, Marine and Fishery Sciences (MAFIS), 37(2), pp. 353–358. doi: 10.47193/mafis.3722024010501.