Journals / Acta Veterinaria Eurasia / 2020 / Cilt: 46 - Sayı: 3

Effect of Seasonality on Oocyte Growth, Oocyte Maturity Stages, and Reproductive Capacity in the Gilthead Sea Bream (Sparus aurata) in Relation with Depth

Pages
87–97
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Findings of this study provide a better understanding of S. aurata breeding pattern and may benefit the management of this highly commercial species.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:This study aimed to investigate the role of seasonal environmental variations in oocyte growth, oocyte maturity stages, and reproductive capacity of Sparus aurata.
📊
Key Findings & Data:To model this in the field, two groups of fish were placed for a 1-year period at two depths: 0-2 m and 10-12 m.
💡
Conclusion & Impact:Findings of this study provide a better understanding of S. aurata breeding pattern and may benefit the management of this highly commercial species.
🔬Design:Modeling & Simulation
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Özet

This study aimed to investigate the role of seasonal environmental variations in oocyte growth, oocyte maturity stages, and reproductive capacity of Sparus aurata. To model this in the field, two groups of fish were placed for a 1-year period at two depths: 0-2 m and 10-12 m. Environmental parameters such as temperature, salinity, pH, dissolved oxygen, and water transparency were monitored, and oocyte number was estimated using standard gravimetric techniques. Oocytes were categorized as primary, cortical alveoli, vitellogenic, hydrated, and atretic and were analyzed according to their shape and diameter. Oocyte maturation period was found to initiate in September and peak in November. During this process, the oocytes appeared to shift from more irregular to elliptical shape. Differences in the oocytes of the two groups, mainly concerning the higher vitellogenic and atretic oocyte number of the 10-12 m group compared with the 0-2 m, supported with gonadosomatic index and hepatosomatic index, might reflect the light intensity and temperature effects. Moreover, using the principal components analysis, we observed a possible link between the environmental temperature and light and the onset of spawning. Findings of this study provide a better understanding of S. aurata breeding pattern and may benefit the management of this highly commercial species.

🔖

Cite This Article

FEIDANTSIS, K., NTOKOU, A., MICHAELIDIS, B. (2020). Effect of Seasonality on Oocyte Growth, Oocyte Maturity Stages, and Reproductive Capacity in the Gilthead Sea Bream (Sparus aurata) in Relation with Depth. Acta Veterinaria Eurasia, Cilt: 46 - Sayı: 3, 87–97. https://ajindex.com/articles/144504

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (1)

  1. Alonso-Fernández, A., Vallejo, A.C., Saborido-Rey, F., Murua, H., Trippel, E.A., 2009. Fecundity estimation of Atlantic cod (Gadus morhua) and haddock (Melanogrammus aeglefinus) of Georges Bank: application of the autodiametric method. Fisheries Research 99, 47-54. [Crossref] Aristizabal, E.O., 2007. Energy investment in the annual reproduction cycle of female red porgy, Pagrus pagrus (L.). Marine Biology 152, 713-724. [Crossref] Bauchot, M.L., Hureau, J.C., Miguel, J.C., 1981. Sparidae. In: W. Fischer, G. Bianchi and W.B. Scott (eds.) FAO Species Identification Sheets For Fishery Purposes. Eastern Central Atlantic. (Fishing Areas 34, 47 (in part)). volume 4. [var. pag.] FAO, Rome. Bell, J.D., Lyle, J.M., Bulman, C.M., Graham, K.J., Newton, G.M., Smith, D.C., 1992. Spatial variation in reproduction, and occurrence of non-reproductive adults, in orange roughy, Hoplostethus atlanticus Collett (Trachichthyidae), from south-eastern Australia. Journal of Fish Biology 40, 107-122. [Crossref] Blazer, V.S., 2002. Histopathological assessment of gonadal tissue in wild fishes. Fish Physiology and Biochemistry 26, 85-101. [Crossref] Boulcott, P.D., Walton, K., Braithwaite, V.A., 2005. The role of ultraviolet wavelengths in the mate-choice decisions of female threespined sticklebacks. Journal of Experimental Biology 208, 1453- 1458. [Crossref] Bozinovic, F., Pörtner, H.O., 2015. Physiological ecology meets climate change. Ecology and Evolution 5, 1025-1030. [Crossref] Brown-Peterson, N.J., Wyanski, D.M., Saborido-Rey, F., Macewicz, B.J., Lowerre-Barbieri, S.K., 2011. A standardized terminology for describing reproductive development in fishes. Marine and Coastal Fisheries 3, 52-70. [Crossref] Brüning, A., Hölker, F., Franke, S., Kleiner, W., Kloas, K., 2016. Impact of different colours of artificial light at night on melatonin rhythm and gene expression of gonadotropins in European perch. Science of Total Environment 543, 214-222. [Crossref] Buxton, C.D., Garratt, P.A., 1990. Alternative reproductive styles in seabreams (Pisces: Sparidae). Environmental Biology of Fishes 28, 113-124. [Crossref] Callow, P., 1985. Adaptative Aspects of Energy allocation In: Tyler, P., Callow, P. (Eds.), Fish Energetics: New Perspectives. Croom Helm Ltd, Sydney, pp. 13-31. [Crossref] Colloca, F., Cerasi, S., 2005. Cultured Aquatic Species Information Programme-Sparus aurata. FAO Inland Water Resources and Aquaculture Service (FIRI). Fisheries and Aquaculture Department, Rome, Italy: FAO.