Development of a new ‘ultrametric’ method for assessing spawning progression in female teleost serial spawners

Abstract The collection and presentation of accurate reproductive data from wild fish has historically been somewhat problematic, especially for serially spawning species. Therefore, the aim of the current study was to develop a novel method of assessing female spawning status that is robust to vari...

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Autores principales: Kelli C. Anderson, Maud Alix, Katerina Charitonidou, Anders Thorsen, Grethe Thorsheim, Kostas Ganias, Thassya C. dos Santos Schmidt, Olav Sigurd Kjesbu
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Publicado: Nature Portfolio 2020
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Acceso en línea:https://doaj.org/article/a18968bde94842b5801b4029aa518d1b
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spelling oai:doaj.org-article:a18968bde94842b5801b4029aa518d1b2021-12-02T17:40:44ZDevelopment of a new ‘ultrametric’ method for assessing spawning progression in female teleost serial spawners10.1038/s41598-020-66601-w2045-2322https://doaj.org/article/a18968bde94842b5801b4029aa518d1b2020-06-01T00:00:00Zhttps://doi.org/10.1038/s41598-020-66601-whttps://doaj.org/toc/2045-2322Abstract The collection and presentation of accurate reproductive data from wild fish has historically been somewhat problematic, especially for serially spawning species. Therefore, the aim of the current study was to develop a novel method of assessing female spawning status that is robust to variation in oocyte dynamics between specimens. Atlantic cod (Barents Sea stock) were used to develop the new ‘ultrametric’ method, that is based on the progressive depletion of the vitellogenic oocyte pool relative to the rather constant previtellogenic oocyte (PVO) pool. Fish were subsequently partitioned into one of four categories that accurately reflected changes in their oocyte size frequency distribution characteristics and gonadosomatic index throughout spawning. The ultrametric method overcomes difficulties associated with presence of bimodal oocyte distributions, oocyte tails, lack of clear hiatus region, and presence of free ova, and can be implemented at a single sampling point. Much of the workflow is fully automated, and the technique may circumvent the need for histological analysis depending on the desired outcome. The ultrametric method differs from the traditional autodiametric method in that PVOs can be separated by ultrasonication and then enumerated, and ovarian homogeneity is not a mandatory requirement per se. The method is designed for determinate spawners but might be extended to include indeterminate spawners.Kelli C. AndersonMaud AlixKaterina CharitonidouAnders ThorsenGrethe ThorsheimKostas GaniasThassya C. dos Santos SchmidtOlav Sigurd KjesbuNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 10, Iss 1, Pp 1-13 (2020)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Kelli C. Anderson
Maud Alix
Katerina Charitonidou
Anders Thorsen
Grethe Thorsheim
Kostas Ganias
Thassya C. dos Santos Schmidt
Olav Sigurd Kjesbu
Development of a new ‘ultrametric’ method for assessing spawning progression in female teleost serial spawners
description Abstract The collection and presentation of accurate reproductive data from wild fish has historically been somewhat problematic, especially for serially spawning species. Therefore, the aim of the current study was to develop a novel method of assessing female spawning status that is robust to variation in oocyte dynamics between specimens. Atlantic cod (Barents Sea stock) were used to develop the new ‘ultrametric’ method, that is based on the progressive depletion of the vitellogenic oocyte pool relative to the rather constant previtellogenic oocyte (PVO) pool. Fish were subsequently partitioned into one of four categories that accurately reflected changes in their oocyte size frequency distribution characteristics and gonadosomatic index throughout spawning. The ultrametric method overcomes difficulties associated with presence of bimodal oocyte distributions, oocyte tails, lack of clear hiatus region, and presence of free ova, and can be implemented at a single sampling point. Much of the workflow is fully automated, and the technique may circumvent the need for histological analysis depending on the desired outcome. The ultrametric method differs from the traditional autodiametric method in that PVOs can be separated by ultrasonication and then enumerated, and ovarian homogeneity is not a mandatory requirement per se. The method is designed for determinate spawners but might be extended to include indeterminate spawners.
format article
author Kelli C. Anderson
Maud Alix
Katerina Charitonidou
Anders Thorsen
Grethe Thorsheim
Kostas Ganias
Thassya C. dos Santos Schmidt
Olav Sigurd Kjesbu
author_facet Kelli C. Anderson
Maud Alix
Katerina Charitonidou
Anders Thorsen
Grethe Thorsheim
Kostas Ganias
Thassya C. dos Santos Schmidt
Olav Sigurd Kjesbu
author_sort Kelli C. Anderson
title Development of a new ‘ultrametric’ method for assessing spawning progression in female teleost serial spawners
title_short Development of a new ‘ultrametric’ method for assessing spawning progression in female teleost serial spawners
title_full Development of a new ‘ultrametric’ method for assessing spawning progression in female teleost serial spawners
title_fullStr Development of a new ‘ultrametric’ method for assessing spawning progression in female teleost serial spawners
title_full_unstemmed Development of a new ‘ultrametric’ method for assessing spawning progression in female teleost serial spawners
title_sort development of a new ‘ultrametric’ method for assessing spawning progression in female teleost serial spawners
publisher Nature Portfolio
publishDate 2020
url https://doaj.org/article/a18968bde94842b5801b4029aa518d1b
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