Influence of maternal effects and temperature on fecundity of Sebastes fasciatus on the Flemish Cap

The conservation of a sufficient reproductive potential of an exploited stock is one of the goals of fisheries management, as it ensures sustainable productivity. However, there is evidence that spawning stock biomass (SSB) does not represent well the variation in stock reproductive potential, often...

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Published in:Scientia Marina
Main Authors: González-Carrión, Francisco, Saborido-Rey, Fran
Format: Article in Journal/Newspaper
Language:English
Published: Consejo Superior de Investigaciones Científicas 2022
Subjects:
Online Access:https://scientiamarina.revistas.csic.es/index.php/scientiamarina/article/view/1939
https://doi.org/10.3989/scimar.05305.050
id ftjscientiamarin:oai:scientiamarina.revistas.csic.es:article/1939
record_format openpolar
institution Open Polar
collection Scientia Marina (E-Journal)
op_collection_id ftjscientiamarin
language English
topic reproductive potential
fish condition
life history
autodiametric method
potencial reproductivo
condición
historia vital
método autodiamétrico
spellingShingle reproductive potential
fish condition
life history
autodiametric method
potencial reproductivo
condición
historia vital
método autodiamétrico
González-Carrión, Francisco
Saborido-Rey, Fran
Influence of maternal effects and temperature on fecundity of Sebastes fasciatus on the Flemish Cap
topic_facet reproductive potential
fish condition
life history
autodiametric method
potencial reproductivo
condición
historia vital
método autodiamétrico
description The conservation of a sufficient reproductive potential of an exploited stock is one of the goals of fisheries management, as it ensures sustainable productivity. However, there is evidence that spawning stock biomass (SSB) does not represent well the variation in stock reproductive potential, often leading to impaired stock-recruitment relationships. In this study we show that fecundity of Sebastes fasciatus on Flemish Cap is not proportional to SSB and shows temporal fluctuation influenced by maternal effects. Females were collected in 23 research surveys between 1996 and 2020. An autodiametric calibration model was developed for S. fasciatus for the first time to estimate fecundity. Mean potential fecundity was estimated as 36000 oocytes and mean relative fecundity as 79 oocytes g–1. Potential fecundity varied significantly with female length, age, condition index, gonadosomatic index and environmental variability. Mixed-effect linear models were fitted to assess the effect of maternal traits and bottom temperature on fecundity. Fecundity increased significantly with condition factor and sea bottom temperature. Relative fecundity also increased significantly with length, age and gonadosomatic index, indicating that older, larger and better-conditioned females produce more eggs per female gram. This suggests that SSB is not a good proxy to stock reproductive potential so it is unsuitable for use in stock assessment and scientific advice. Considering that S. fasciatus is a viviparous species, future research should focus on maternal effects on offspring and on building time series of reproductive potential indexes that take into account maternal effects. La conservación de un potencial reproductivo suficiente de una población explotada es uno de los objetivos de la gestión pesquera, ya que garantiza la consecución de una productividad sostenible. El establecimiento de relaciones fiables stock-reclutamiento es esencial para lograr este objetivo, pero la biomasa reproductora (SSB) se utiliza a menudo como ...
format Article in Journal/Newspaper
author González-Carrión, Francisco
Saborido-Rey, Fran
author_facet González-Carrión, Francisco
Saborido-Rey, Fran
author_sort González-Carrión, Francisco
title Influence of maternal effects and temperature on fecundity of Sebastes fasciatus on the Flemish Cap
title_short Influence of maternal effects and temperature on fecundity of Sebastes fasciatus on the Flemish Cap
title_full Influence of maternal effects and temperature on fecundity of Sebastes fasciatus on the Flemish Cap
title_fullStr Influence of maternal effects and temperature on fecundity of Sebastes fasciatus on the Flemish Cap
title_full_unstemmed Influence of maternal effects and temperature on fecundity of Sebastes fasciatus on the Flemish Cap
title_sort influence of maternal effects and temperature on fecundity of sebastes fasciatus on the flemish cap
publisher Consejo Superior de Investigaciones Científicas
publishDate 2022
url https://scientiamarina.revistas.csic.es/index.php/scientiamarina/article/view/1939
https://doi.org/10.3989/scimar.05305.050
genre Arctic
genre_facet Arctic
op_source Scientia Marina; Vol. 86 No. 4 (2022); e050
Scientia Marina; Vol. 86 Núm. 4 (2022); e050
1886-8134
0214-8358
10.3989/scimar.2022.86n4
op_relation https://scientiamarina.revistas.csic.es/index.php/scientiamarina/article/view/1939/2916
https://scientiamarina.revistas.csic.es/index.php/scientiamarina/article/view/1939/2917
https://scientiamarina.revistas.csic.es/index.php/scientiamarina/article/view/1939/2918
Alonso-Fernández, A., Vallejo, A. C., Saborido-Rey, F., et al. 2009. Fecundity estimation of Atlantic cod (Gadus morhua) and haddock (Melanogrammus aeglefinus) of Georges Bank: Application of the autodiametric method. Fish. Res. 99: 47-54.
Anderson C.N.K., Hsieh C.H., Sandin S.A. et al. 2008. Why fishing magnifies fluctuations in fish abundance. Nature 452: 835-839.
Armstrong M.J, Witthames P.R. 2012. Developments in understanding of fecundity of fish stocks in relation to egg production methods for estimating spawning stock biomass. Fish. Res. 117/118: 35-47.
Berkeley S.A., Bobko S.J. 2004. Maturity, ovarian cycle, fecundity, and age-specific parturition of black rockfish (Sebastes melanops). Fish. Bull. 102: 418-429.
Beyer S.G., Sogard S.M., Harvey C. J., Field J.C. 2015. Variability in rockfish (Sebastes spp.) fecundity: species contrasts, maternal size effects, and spatial differences. Environ. Biol. Fish. 98: 81-100.
Blanchard J.L., Frank K.T., Simon J.E. 2003. Effects of condition on fecundity and total egg production of eastern Scotian Shelf haddock (Melanogrammus aeglefinus). Can. J. Fish. Aquat. Sci. 60: 321-332.
Brown-Peterson N.J., Wyanski D.M., Saborido-Rey F., et al. 2011. A standardized terminology for describing reproductive development in fishes. Mar. Coast. Fish. 3: 52-70.
Brooks M. E., Kristensen K., van Benthem K. J., et al. 2017. glmmTMB Balances Speed and Flexibility Among Packages for Zero-inflated Generalized Linear Mixed Modeling. The R Journal 9: 378-400.
Chang H. Y., Richards R. A., Chen Y. 2021. Effects of environmental factors on reproductive potential of the Gulf of Maine northern shrimp (Pandalus borealis). GECCO 30: e01774.
Cheung W. Lam W. L., Sarmiento V.W.Y., et al. 2009. Projecting global marine biodiversity impacts under climate Change scenarios. Fish Fish. 10: 235-251.
Colbourne E., Perez-Rodriguez A., Cabrero A., Gonzalez-Nuevo G. 2018. Ocean Climate Variability on the Flemish Cap in NAFO Subdivision 3M during 2017 June.
Dick E. J. 2009. University of California Santa Cruz modeling the reproductive potential of rockfishes, 299 pp.
Dominguez-Petit R., Rideout R.M., Garabana D., et al. 2018. Evaluating the use of the autodiametric method for estimating fecundity of Reinhardtius hippoglossoides, a species with an unusual oocyte development strategy. ICES J. Mar. Sci. 75: 831-839.
Fisher R, Sogard S.M, Berkeley S.A. 2007 Trade-offs between size and energy reserves reflect alternative strategies for optimizing larval survival potential in rockfish. Mar. Ecol. Prog. Ser. 344: 257-270.
Friedland K.D., Ama-Abasi D., Manning M., et al. 2005. Automated egg counting and sizing from scanned images: Rapid sample processing and large data volumes for fecundity estimates. J. Sea. Res. 54: 307-316.
Hsieh C.H, Reiss C.S, Hunter J.R, et al. 2006. Fishing elevates variability in the abundance of exploited species. Nature 443: 859-862.
González-Troncoso D., Garrido I. Rábade S., et al. 2022. Results from Bottom Trawl Survey on Flemish Cap of June-July 2021. NAFO SCR Doc. 22/004.
Kennedy J., Witthames P.R., Nash R.D.M. 2007. The concept of fecundity regulation in plaice (Pleuronectes platessa) tested on three Irish Sea spawning populations. Can. J. Fish. Aquat. Sci. 64: 587-601.
Kraus G., Müller A., Trella K., Köster F.W. 2000. Fecundity of Baltic cod: Temporal and spatial variation. J. Fish. Biol. 56: 1327-1341.
Kraus G., Tomkiewicz J., Köster F.W. 2002. Egg production of Baltic cod (Gadus morhua) in relation to variable sex ratio, maturity, and fecundity. Can. J. Fish. Aquat. Sci. 59:1908-1920.
Lambert Y. 2008). Why should we closely monitor fecundity in marine fish populations? J. Northwest. Atl. Fish. Soc: 41: 93-106.
Lambert Y., Yaragina N. A., Kraus G., et al. 2003. Using environmental and biological indices as proxies for egg and larval production of marine fish. J. Northwest. Atl. Fish. Soc. 33: 115-159.
Marteinsdottir G., Begg G. A. 2002. Essential relationships incorporating the influence of age, size and condition on variables required for estimation of reproductive potential in Atlantic cod Gadus morhua. Mar. Ecol. Prog. Ser. 235: 235-256.
Marteinsdottir G., Thorarinsson K. 1998. Improving the stock-recruitment relationship in Icelandic cod (Gadus morhua) by including age diversity of spawners. Can. J. Fish. Aquat. Sci. 55: 1372-1377.
McElroy W.D., Wuenschel M.J., Press Y.K., et al. 2013. Differences in female individual reproductive potential among three stocks of winter flounder, Pseudopleuronectes americanus. J. Sea. Res. 75: 52-61.
Mion M., Thorsen A., Vitale F., et al. 2018. Effect of fish length and nutritional condition on the fecundity of distressed Atlantic cod Gadus morhua from the Baltic Sea. J. Fish. Biol. 92: 1016-1034.
Murua H., Saborido-Rey F. 2003. Female Reproductive Strategies of Marine Fish Species of the North Atlantic. J. Northwest. Atl. Fish. Soc. 33: 23-31.
Nichol D.G., Acuna E.I. 2001. Annual and batch fecundities of yellow fin sole, Limanda aspera, in the Eastern Bering Sea. Fish. Bull. U.S. 99: 108-122.
R Core Team. 2020 R: A Language and Environment for Statistical Computing. R Foundation for Statistical Computing, Vienna, Austria.
Rideout R.M, Morgan M.J. 2010. Relationships between maternal body size, condition and potential fecundity of four northwest Atlantic demersal fishes. J. Fish. Biol. 76: 1379-1395.
Román S., Weidberg N., Muñiz C., et al. 2022. Mesoscale patterns in barnacle reproduction are mediated by upwelling-driven thermal variability. Mar. Ecol. Prog. Ser. 685: 153-170.
Saborido-Rey F., Domínguez-Petit R., Garabana D., Sigurðsson Þ. 2015. Fecundity of Sebastes mentella and Sebastes norvegicus in the Irminger Sea and Icelandic waters. Sci. Mar., 41: 107-124.
Saborido-Rey F., Trippel E.A. 2013. Fish reproduction and fisheries. Fish. Res. 138: 1-4.
Sogard S. M., Berkeley S.A., Fisher R. 2008. Maternal effects in rockfishes Sebastes spp.: A comparison among species. Mar. Ecol. Prog. Ser. 360: 227-236.
Stafford D.M., Sogard S.M., Berkeley S.A. 2014. Maternal influence on timing of parturition, fecundity, and larval quality in three shelf rockfishes (Sebastes spp.). Aquat. Biol. 21: 11-24.
Thorsen A., Kjesbu O.S. 2001. A rapid method for estimation of oocyte size and potential fecundity in Atlantic cod using a computer-aided particle analysis system. J. Sea. Res. 46: 295-308.
Thorsen A., Marshall C.T., Kjesbu O.S. 2006. Comparison of various potential fecundity models for north-east Arctic cod Gadus morhua, L. using oocyte diameter as a standardizing factor. J. Sea. Res. 69: 1709-1730.
Tomkiewicz J., Morgan M.J., Burnett J. Saborido-Rey F. 2003. Available information for estimating reproductive potential of northwest Atlantic groundfish stocks. J. Northwest. Atl. Fish. Soc. 33: 1-21
Witthames P.R., Thorsen A., Murua H., et al. 2009. Advances in methods for determining fecundity: application of the new methods to some marine fishes. Fish. Bull. 107: 148-164.
Yoneda M., Wright P.J. 2004. Temporal and spatial variation in reproductive investment of Atlantic cod Gadus morhua in the northern North Sea and Scottish west coast. Mar. Ecol. Prog. Ser. 276: 237-248.
Zuur A.F., Ieno E.N. 2013. Mixed effects Models and Extensions in Ecology with R. In Journal of Chemical Information and Modeling. 53(9).
https://scientiamarina.revistas.csic.es/index.php/scientiamarina/article/view/1939
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spelling ftjscientiamarin:oai:scientiamarina.revistas.csic.es:article/1939 2023-05-15T14:28:27+02:00 Influence of maternal effects and temperature on fecundity of Sebastes fasciatus on the Flemish Cap Influencia de los efectos maternales y la temperatura en la fecundidad de Sebastes fasciatus en Flemish Cap González-Carrión, Francisco Saborido-Rey, Fran 2022-12-14 text/html application/pdf text/xml https://scientiamarina.revistas.csic.es/index.php/scientiamarina/article/view/1939 https://doi.org/10.3989/scimar.05305.050 eng eng Consejo Superior de Investigaciones Científicas https://scientiamarina.revistas.csic.es/index.php/scientiamarina/article/view/1939/2916 https://scientiamarina.revistas.csic.es/index.php/scientiamarina/article/view/1939/2917 https://scientiamarina.revistas.csic.es/index.php/scientiamarina/article/view/1939/2918 Alonso-Fernández, A., Vallejo, A. C., Saborido-Rey, F., et al. 2009. Fecundity estimation of Atlantic cod (Gadus morhua) and haddock (Melanogrammus aeglefinus) of Georges Bank: Application of the autodiametric method. Fish. Res. 99: 47-54. Anderson C.N.K., Hsieh C.H., Sandin S.A. et al. 2008. Why fishing magnifies fluctuations in fish abundance. Nature 452: 835-839. Armstrong M.J, Witthames P.R. 2012. Developments in understanding of fecundity of fish stocks in relation to egg production methods for estimating spawning stock biomass. Fish. Res. 117/118: 35-47. Berkeley S.A., Bobko S.J. 2004. Maturity, ovarian cycle, fecundity, and age-specific parturition of black rockfish (Sebastes melanops). Fish. Bull. 102: 418-429. Beyer S.G., Sogard S.M., Harvey C. J., Field J.C. 2015. Variability in rockfish (Sebastes spp.) fecundity: species contrasts, maternal size effects, and spatial differences. Environ. Biol. Fish. 98: 81-100. Blanchard J.L., Frank K.T., Simon J.E. 2003. Effects of condition on fecundity and total egg production of eastern Scotian Shelf haddock (Melanogrammus aeglefinus). Can. J. Fish. Aquat. Sci. 60: 321-332. Brown-Peterson N.J., Wyanski D.M., Saborido-Rey F., et al. 2011. A standardized terminology for describing reproductive development in fishes. Mar. Coast. Fish. 3: 52-70. Brooks M. E., Kristensen K., van Benthem K. J., et al. 2017. glmmTMB Balances Speed and Flexibility Among Packages for Zero-inflated Generalized Linear Mixed Modeling. The R Journal 9: 378-400. Chang H. Y., Richards R. A., Chen Y. 2021. Effects of environmental factors on reproductive potential of the Gulf of Maine northern shrimp (Pandalus borealis). GECCO 30: e01774. Cheung W. Lam W. L., Sarmiento V.W.Y., et al. 2009. Projecting global marine biodiversity impacts under climate Change scenarios. Fish Fish. 10: 235-251. Colbourne E., Perez-Rodriguez A., Cabrero A., Gonzalez-Nuevo G. 2018. Ocean Climate Variability on the Flemish Cap in NAFO Subdivision 3M during 2017 June. Dick E. J. 2009. University of California Santa Cruz modeling the reproductive potential of rockfishes, 299 pp. Dominguez-Petit R., Rideout R.M., Garabana D., et al. 2018. Evaluating the use of the autodiametric method for estimating fecundity of Reinhardtius hippoglossoides, a species with an unusual oocyte development strategy. ICES J. Mar. Sci. 75: 831-839. Fisher R, Sogard S.M, Berkeley S.A. 2007 Trade-offs between size and energy reserves reflect alternative strategies for optimizing larval survival potential in rockfish. Mar. Ecol. Prog. Ser. 344: 257-270. Friedland K.D., Ama-Abasi D., Manning M., et al. 2005. Automated egg counting and sizing from scanned images: Rapid sample processing and large data volumes for fecundity estimates. J. Sea. Res. 54: 307-316. Hsieh C.H, Reiss C.S, Hunter J.R, et al. 2006. Fishing elevates variability in the abundance of exploited species. Nature 443: 859-862. González-Troncoso D., Garrido I. Rábade S., et al. 2022. Results from Bottom Trawl Survey on Flemish Cap of June-July 2021. NAFO SCR Doc. 22/004. Kennedy J., Witthames P.R., Nash R.D.M. 2007. The concept of fecundity regulation in plaice (Pleuronectes platessa) tested on three Irish Sea spawning populations. Can. J. Fish. Aquat. Sci. 64: 587-601. Kraus G., Müller A., Trella K., Köster F.W. 2000. Fecundity of Baltic cod: Temporal and spatial variation. J. Fish. Biol. 56: 1327-1341. Kraus G., Tomkiewicz J., Köster F.W. 2002. Egg production of Baltic cod (Gadus morhua) in relation to variable sex ratio, maturity, and fecundity. Can. J. Fish. Aquat. Sci. 59:1908-1920. Lambert Y. 2008). Why should we closely monitor fecundity in marine fish populations? J. Northwest. Atl. Fish. Soc: 41: 93-106. Lambert Y., Yaragina N. A., Kraus G., et al. 2003. Using environmental and biological indices as proxies for egg and larval production of marine fish. J. Northwest. Atl. Fish. Soc. 33: 115-159. Marteinsdottir G., Begg G. A. 2002. Essential relationships incorporating the influence of age, size and condition on variables required for estimation of reproductive potential in Atlantic cod Gadus morhua. Mar. Ecol. Prog. Ser. 235: 235-256. Marteinsdottir G., Thorarinsson K. 1998. Improving the stock-recruitment relationship in Icelandic cod (Gadus morhua) by including age diversity of spawners. Can. J. Fish. Aquat. Sci. 55: 1372-1377. McElroy W.D., Wuenschel M.J., Press Y.K., et al. 2013. Differences in female individual reproductive potential among three stocks of winter flounder, Pseudopleuronectes americanus. J. Sea. Res. 75: 52-61. Mion M., Thorsen A., Vitale F., et al. 2018. Effect of fish length and nutritional condition on the fecundity of distressed Atlantic cod Gadus morhua from the Baltic Sea. J. Fish. Biol. 92: 1016-1034. Murua H., Saborido-Rey F. 2003. Female Reproductive Strategies of Marine Fish Species of the North Atlantic. J. Northwest. Atl. Fish. Soc. 33: 23-31. Nichol D.G., Acuna E.I. 2001. Annual and batch fecundities of yellow fin sole, Limanda aspera, in the Eastern Bering Sea. Fish. Bull. U.S. 99: 108-122. R Core Team. 2020 R: A Language and Environment for Statistical Computing. R Foundation for Statistical Computing, Vienna, Austria. Rideout R.M, Morgan M.J. 2010. Relationships between maternal body size, condition and potential fecundity of four northwest Atlantic demersal fishes. J. Fish. Biol. 76: 1379-1395. Román S., Weidberg N., Muñiz C., et al. 2022. Mesoscale patterns in barnacle reproduction are mediated by upwelling-driven thermal variability. Mar. Ecol. Prog. Ser. 685: 153-170. Saborido-Rey F., Domínguez-Petit R., Garabana D., Sigurðsson Þ. 2015. Fecundity of Sebastes mentella and Sebastes norvegicus in the Irminger Sea and Icelandic waters. Sci. Mar., 41: 107-124. Saborido-Rey F., Trippel E.A. 2013. Fish reproduction and fisheries. Fish. Res. 138: 1-4. Sogard S. M., Berkeley S.A., Fisher R. 2008. Maternal effects in rockfishes Sebastes spp.: A comparison among species. Mar. Ecol. Prog. Ser. 360: 227-236. Stafford D.M., Sogard S.M., Berkeley S.A. 2014. Maternal influence on timing of parturition, fecundity, and larval quality in three shelf rockfishes (Sebastes spp.). Aquat. Biol. 21: 11-24. Thorsen A., Kjesbu O.S. 2001. A rapid method for estimation of oocyte size and potential fecundity in Atlantic cod using a computer-aided particle analysis system. J. Sea. Res. 46: 295-308. Thorsen A., Marshall C.T., Kjesbu O.S. 2006. Comparison of various potential fecundity models for north-east Arctic cod Gadus morhua, L. using oocyte diameter as a standardizing factor. J. Sea. Res. 69: 1709-1730. Tomkiewicz J., Morgan M.J., Burnett J. Saborido-Rey F. 2003. Available information for estimating reproductive potential of northwest Atlantic groundfish stocks. J. Northwest. Atl. Fish. Soc. 33: 1-21 Witthames P.R., Thorsen A., Murua H., et al. 2009. Advances in methods for determining fecundity: application of the new methods to some marine fishes. Fish. Bull. 107: 148-164. Yoneda M., Wright P.J. 2004. Temporal and spatial variation in reproductive investment of Atlantic cod Gadus morhua in the northern North Sea and Scottish west coast. Mar. Ecol. Prog. Ser. 276: 237-248. Zuur A.F., Ieno E.N. 2013. Mixed effects Models and Extensions in Ecology with R. In Journal of Chemical Information and Modeling. 53(9). https://scientiamarina.revistas.csic.es/index.php/scientiamarina/article/view/1939 doi:10.3989/scimar.05305.050 Copyright (c) 2022 Consejo Superior de Investigaciones Científicas (CSIC) https://creativecommons.org/licenses/by/4.0 CC-BY Scientia Marina; Vol. 86 No. 4 (2022); e050 Scientia Marina; Vol. 86 Núm. 4 (2022); e050 1886-8134 0214-8358 10.3989/scimar.2022.86n4 reproductive potential fish condition life history autodiametric method potencial reproductivo condición historia vital método autodiamétrico info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion Peer-reviewed article Artículo revisado por pares 2022 ftjscientiamarin https://doi.org/10.3989/scimar.05305.050 https://doi.org/10.3989/scimar.2022.86n4 2022-12-21T00:40:41Z The conservation of a sufficient reproductive potential of an exploited stock is one of the goals of fisheries management, as it ensures sustainable productivity. However, there is evidence that spawning stock biomass (SSB) does not represent well the variation in stock reproductive potential, often leading to impaired stock-recruitment relationships. In this study we show that fecundity of Sebastes fasciatus on Flemish Cap is not proportional to SSB and shows temporal fluctuation influenced by maternal effects. Females were collected in 23 research surveys between 1996 and 2020. An autodiametric calibration model was developed for S. fasciatus for the first time to estimate fecundity. Mean potential fecundity was estimated as 36000 oocytes and mean relative fecundity as 79 oocytes g–1. Potential fecundity varied significantly with female length, age, condition index, gonadosomatic index and environmental variability. Mixed-effect linear models were fitted to assess the effect of maternal traits and bottom temperature on fecundity. Fecundity increased significantly with condition factor and sea bottom temperature. Relative fecundity also increased significantly with length, age and gonadosomatic index, indicating that older, larger and better-conditioned females produce more eggs per female gram. This suggests that SSB is not a good proxy to stock reproductive potential so it is unsuitable for use in stock assessment and scientific advice. Considering that S. fasciatus is a viviparous species, future research should focus on maternal effects on offspring and on building time series of reproductive potential indexes that take into account maternal effects. La conservación de un potencial reproductivo suficiente de una población explotada es uno de los objetivos de la gestión pesquera, ya que garantiza la consecución de una productividad sostenible. El establecimiento de relaciones fiables stock-reclutamiento es esencial para lograr este objetivo, pero la biomasa reproductora (SSB) se utiliza a menudo como ... Article in Journal/Newspaper Arctic Scientia Marina (E-Journal) Scientia Marina 86 4 e050