Skip to main content
Log in

Effects of varying densities on serum reproductive parameters in pen-reared juvenile female rainbow trout Oncorhynchus mykiss farms

  • Biology
  • Published:
Chinese Journal of Oceanology and Limnology Aims and scope Submit manuscript

An Erratum to this article was published on 07 March 2017

Abstract

The primary goal of this study was to assess the effect of varying densities on serum reproductive parameters of immature rainbow trout Oncorhynchus mykiss. Experimental trout were maintained in intensive, pen-reared farms for 300 days in fresh water reservoirs. Initial densities were 4.6, 6.6, and 8.6 kg/m3 (40, 60, 80 ind./m3), indicated as SD1, SD2, SD3, and final densities were 31.1, 40.6, 49.3 kg/m3, respectively. A summary of the ovarian stages were observed by histological examination. Serum E2 (estradiol), T (testosterone) were evaluated by radioimmunoassay and FSH (follicle-stimulating-hormone), LH (luteinizing-hormone), vitellogenin, 17α,20β-P (17α,20βdihydroxy4-pregnen-3-one) were measured by enzyme-linked immunosorbent assay. Our findings demonstrated that ovarian development were retarded (from stage III to stage IV) at highest rearing density (SD3) after 180 days of intensive culture (over 40.6 kg/m3). In addition, we observed an inverse relationship between serum reproductive parameters and rearing density. Furthermore, compared to serum reproductive parameters of SD1, E2, T, FSH, vitellogenin, 17α,20β-P, GSI and LH of two higher density groups decreased firstly and significantly at 60 (over 15.9 kg/m 3 ), 180 (over 31.7 kg/m 3 ), 180 (over 40.6 kg/m3), 240 (over 36 kg/m3), 240 (over 36 kg/m3), 240 (over 45 kg/m3) and 300 (over 49.3 kg/m3) days, respectively. Comparing serum reproductive parameters within the same ovarian development stage of rainbow trout from varying densities revealed that higher population density also led to significantly lower overall serum reproductive parameters. Overall, this study presents the reproductive, endocrinological parameters of juvenile female rainbow trout at high rearing densities and indicates the need for rainbow trout (114.44±5.21 g, 19.69±0.31 cm) that are initially stocked at 6.6 or 8.6 kg/m3 should be classified and subdivided into lower density after 180 days of farming (not over 31.7 kg/m3).

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Andersson E, Schulz R W, Male R et al. 2013. Pituitary gonadotropin and ovarian gonadotropin receptor transcript levels: seasonal and photoperiod-induced changes in the reproductive physiology of female Atlantic salmon (Salmo salar). General and Comparative Endocrinology, 191: 247–258.

    Article  Google Scholar 

  • Andrade T, Afonso A, érez-Jiménez A et al. 2015. Evaluation of different stocking densities in a Senegalese sole (Solea senegalensis) farm: implications for growth, humoral immune parameters and oxidative status. Aquaculture, 438: 6–11.

    Article  Google Scholar 

  • Atteke C, Vetillard A, Fostier A et al. 2003. effects of progesterone and estradiol on the reproductive axis in immature diploid and triploid rainbow trout. Comparative Biochemistry and Physiology Part A: Molecular & Integrative Physiology, 134 (4): 693–705.

    Article  Google Scholar 

  • Bekhit A E D A, Morton J D, Dawson C O, Zhao J H, Lee H Y Y. 2009. Impact of maturity on the physicochemical and biochemical properties of chinook salmon roe. Food Chemistry, 117 (2): 318–325.

    Article  Google Scholar 

  • Berg A J, Sigholt T, Seland A, Danielsberg A. 1996. effect of stocking density, oxygen level, light regime and swimming velocity on the incidence of sexual maturation in adult Atlantic salmon (Salmo salar). Aquaculture, 143 (1): 43–59.

    Article  Google Scholar 

  • Di Marco P, Priori A, Finoia M G et al. 2008. Physiological responses of European sea bass Dicentrarchus labrax to different stocking densities and acute stress challenge. Aquaculture, 275 (1-4): 319–328.

    Article  Google Scholar 

  • Ellis T, North B, Scott A P, Bromage N R, Porter M, Gadd D. 2002. The relationships between stocking density and welfare in farmed rainbow trout. Journal of Fish Biology, 61 (3): 493–531.

    Article  Google Scholar 

  • Jørgensen E H, Christiansen J S, Jobling M. 1993. effects of stocking density on food intake, growth performance and oxygen consumption in Arctic charr (Salvelinus alpinus). Aquaculture, 110 (2): 191–204.

    Article  Google Scholar 

  • Kagawa H, Takano K, Nagahama Y. 1981. Correlation of plasma estradiol-17ß and progesterone levels with ultrastructure and histochemistry of ovarian follicles in the white-spotted char, Salvelinus leucomaenis. Cell and Tissue Research, 218 (2): 315–329.

    Article  Google Scholar 

  • King H R, Pankhurst N W. 2003. Ovarian growth and plasma sex steroid and vitellogenin profiles during vitellogenesis in Tasmanian female Atlantic salmon (Salmo salar). Aquaculture, 219 (1-4): 797–813.

    Article  Google Scholar 

  • Larsen B K, Skov P V, McKenzie D J et al. 2012. The effects of stocking density and low level sustained exercise on the energetic efficiency of rainbow trout (Oncorhynchus mykiss) reared at 19°C. Aquaculture, 324-325: 226–233.

    Article  Google Scholar 

  • Laursen D C, Silva P I M, Larsen B K et al. 2013. High oxygen consumption rates and scale loss indicate elevated aggressive behaviour at low rearing density, while elevated brain serotonergic activity suggests chronic stress at high rearing densities in farmed rainbow trout. Physiology & Behavior, 122: 147–154.

    Article  Google Scholar 

  • Leatherland J F, Cho C Y. 1985. effect of rearing density on thyroid and interrenal gland activity and plasma hepatic metabolite levels in rainbow trout, Salmo gairdneri, Richardson. Journal of Fish Biology, 27 (5): 583–592.

    Article  Google Scholar 

  • Levavi-Sivan B, Bogerd J, Mañanós E L et al. 2010. Perspectives on fish gonadotropins and their receptors. General and Comparative Endocrinology, 165 (3): 412–437.

    Article  Google Scholar 

  • Luckenbach J A, Yamamoto Y, Guzmán J M et al. 2013. Identification of ovarian genes regulated by folliclestimulating hormone (Fsh) in vitro during early secondary oocyte growth in coho salmon. Molecular and Cellular Endocrinology, 366 (1): 38–52.

    Article  Google Scholar 

  • Morgan A L, Thompson K D, Auchinachie N A et al. 2008. The effect of seasonality on normal haematological and innate immune parameters of rainbow trout Oncorhynchus mykiss L. Fish & Shellfish Immunology, 25 (6): 791–799.

    Article  Google Scholar 

  • Nagahama Y, Yamashita M. 2008. Regulation of oocyte maturation in fish. Development, Growth & Differentiation, 50 (S1): S195–S219.

    Article  Google Scholar 

  • Nagahama Y. 1994. Endocrine regulation of gametogenesis in fish. International Journal of Developmental Biology, 38 (2): 217–229.

    Google Scholar 

  • Nagler J J, Cavileer T D, Verducci J S et al. 2012. Estrogen receptor mRNA expression patterns in the liver and ovary of female rainbow trout over a complete reproductive cycle. General and Comparative Endocrinology, 178 (3): 556–561.

    Article  Google Scholar 

  • Nelson E R, Habibi H R. 2010. Functional significance of nuclear estrogen receptor subtypes in the liver of goldfish. Endocrinology, 151 (4): 1668–1676.

    Article  Google Scholar 

  • Oppen-Berntsen D O, Olsen S O, Rong C J et al. 1994. Plasma levels of eggshell zr-proteins, estradiol-17ß, and gonadotropins during an annual reproductive cycle of Atlantic salmon (Salmo salar). Journal of Experimental Zoology, 268 (1): 59–70.

    Article  Google Scholar 

  • Pramanick K, Kundu S, Paul S et al. 2013. Changes in plasma steroid levels during oocyte development in Indian shad, Tenualosa ilisha (Hamilton, 1822): role of gonadotropins on in vitro steroid production and development of oocyte maturational competence. Animal Reproduction Science, 141 (3-4): 177–188.

    Article  Google Scholar 

  • Richards J A S. 1994. Hormonal control of gene expression in the ovary. Endocrine Reviews, 15 (6): 725–751.

    Article  Google Scholar 

  • Rodrigo J, Ros G, Periago M, López C, Ortuño J. 1998. Proximate and mineral composition of dried salted roes of hake (Merluccius merluccius, L.) and ling (Molva molva, L.). Food Chemistry, 63 (2): 221–225.

    Article  Google Scholar 

  • Sahin K, Yazlak H, Orhan C et al. 2014. The effect of lycopene on antioxidant status in rainbow trout (Oncorhynchus mykiss) reared under high stocking density. Aquaculture, 418-419: 132–138.

    Article  Google Scholar 

  • Schubring R. 2004. Differential scanning calorimetric (DSC) measurements on the roe of rainbow trout (Oncorhynchus mykiss): influence of maturation and technological treatment. Thermochimica Acta, 415 (1-2): 89–98.

    Article  Google Scholar 

  • Sen U, Mukherjee D, Bhattacharyya S P et al. 2002. Seasonal changes in plasma steroid levels in Indian major carp Labeo rohita: influence of homologous pituitary extract on steroid production and development of oocyte maturational competence. General and Comparative Endocrinology, 128 (2): 123–134.

    Article  Google Scholar 

  • Siikavuopio S I, Dale T, Mortensen A. 2007. The effects of stocking density on gonad growth, survival and feed intake of adult green sea urchin (Strongylocentrotus droebachiensis). Aquaculture, 262 (1): 78–85.

    Article  Google Scholar 

  • Skov P V, Larsen B K, Frisk M et al. 2011. effects of rearing density and water current on the respiratory physiology and haematology in rainbow trout, Oncorhynchus mykiss at high temperature. Aquaculture, 319 (3-4): 446–452.

    Article  Google Scholar 

  • Sternin V, Dore I. 1993. Caviar: the Resource Book. Cultura, Stanwood, WA, US.

    Google Scholar 

  • Swanson P, Dickey J T, Campbell B. 2003. Biochemistry and physiology of fish gonadotropins. Fish Physiology and Biochemistry, 28 (1-4): 53–59.

    Article  Google Scholar 

  • Thomas P. 1994. Hormonal control of final oocyte maturation in sciaenid fishes. In: Davy K G ed. Perspectives in Comparative Endocrinology. National Research Council of Canada, Ottawa, p.619–625.

    Google Scholar 

  • Wen H S, Song H X, Yang L T et al. 2006. A study on the effects of exogenous hormone on the plasma testosterone and estradiol levels in cultured Japanese flounder. Acta Oceanologica Sinica, 28 (4): 115–120. (in Chinese with English abstract)

    Google Scholar 

  • Yoshikuni M, Shibata N, Nagahama Y. 1993. Specific binding of [3 H] 17a, 20ß-dihydroxy-4-pregnen-3-one to oocyte cortices of rainbow trout (Oncorhynchus mykiss). Fish Physiology and Biochemistry, 11 (1-6): 15–24.

    Article  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Haishen Wen  (温海深).

Additional information

Supported by the Special Fund for Agro-Scientific Research in the Public Interest (No. 201003055)

An erratum to this article is available at http://dx.doi.org/10.1007/s00343-017-7466-6.

Electronic supplementary material

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Hou, Z., Wen, H., Li, J. et al. Effects of varying densities on serum reproductive parameters in pen-reared juvenile female rainbow trout Oncorhynchus mykiss farms. Chin. J. Ocean. Limnol. 35, 98–108 (2017). https://doi.org/10.1007/s00343-016-5172-4

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00343-016-5172-4

Keywords

Navigation