Hostname: page-component-78c5997874-ndw9j Total loading time: 0 Render date: 2024-11-05T04:55:00.473Z Has data issue: false hasContentIssue false

Influence of batch-specific biochemical egg characteristics on embryogenesis and hatching success in farmed pikeperch

Published online by Cambridge University Press:  04 December 2017

F. J. Schaefer*
Affiliation:
Department of Ecophysiology and Aquaculture, Leibniz-Institute of Freshwater Ecology and Inland Fisheries, Müggelseedamm 310, 12587 Berlin, Germany Albrecht Daniel Thaer-Institute of Agricultural and Horticultural Sciences, Faculty of Life Sciences, Humboldt University, Invalidenstraße, 42, 10115 Berlin, Germany
J. L. Overton
Affiliation:
AquaPri Denmark A/S, Egtved 6040, Denmark
A. Krüger
Affiliation:
Department of Chemical Analytics and Biogeochemistry, Leibniz-Institute of Freshwater Ecology and Inland Fisheries, Müggelseedamm 310, 12587 Berlin, Germany
W. Kloas
Affiliation:
Department of Ecophysiology and Aquaculture, Leibniz-Institute of Freshwater Ecology and Inland Fisheries, Müggelseedamm 310, 12587 Berlin, Germany Albrecht Daniel Thaer-Institute of Agricultural and Horticultural Sciences, Faculty of Life Sciences, Humboldt University, Invalidenstraße, 42, 10115 Berlin, Germany Department of Biology, Faculty of Life Sciences, Humboldt University Berlin, Invalidenstraße 110, 10115 Berlin, Germany
S. Wuertz
Affiliation:
Department of Ecophysiology and Aquaculture, Leibniz-Institute of Freshwater Ecology and Inland Fisheries, Müggelseedamm 310, 12587 Berlin, Germany Albrecht Daniel Thaer-Institute of Agricultural and Horticultural Sciences, Faculty of Life Sciences, Humboldt University, Invalidenstraße, 42, 10115 Berlin, Germany
*
Get access

Abstract

Low and variable egg quality remains a major issue in aquaculture impeding a reliable and continuous supply of larvae, particularly in emerging species, such as pikeperch, Sander lucioperca. We assessed the influence of batch-specific egg parameters (fatty acid (FA) profiles, cortisol content) on embryo life-stages until hatching (survival at 2, 24, 48, 72 h post fertilization (hpf), hatching rate) in an integrated study under commercial hatchery conditions (44 egg batches). Embryo mortality was elevated until 48 hpf (average 9.8% mortality between 2 and 48 hpf). Embryos surviving until 48 hpf were very likely (98.5%) to hatch successfully. The inherent egg FA composition was variable in-between batches. Total FA content ranged form 66.1 to 171.7 µg/mg (dry matter) total FA. Whereas specific FA ,18 : 0 and 20 : 5(n-3) (eicosapentaenoic acid) of the polar fraction and the ratio of 22 : 6(n-3) (docosahexaenoic acid) to 20 : 5(n-3) within the neutral fraction, were significantly correlated with early embryo development, contents of the respective FA did not differ between high (>90% hatching rate), mid (70% to 90% hatching rate) and low (<70% hatching rate) quality egg batches. Late embryo development and hatching were relatively independent of the FA profiles highlighting stage-dependent influences especially during early embryogenesis. Cortisol levels ranged from 22.7 to 293.2 ng/ml and did not directly explain for mortalities. However, high cortisol was associated with a lower content of specific FA, in particular highly unsaturated FA. These results demonstrate the magnitude of inter-individual differences in the batch-specific biochemical egg composition under stable hatchery conditions and suggest a stress-mediated lack of essential FA, which in turn affects early embryo survival. Surprisingly, embryos are able to cope well with a broad range of inherent egg parameters, which limits their predictive potential for egg quality in general. Still, specific FA profiles of high quality egg batches have potential for formulating species-specific broodstock diets and improving reproductive management in pikeperch.

Type
Research Article
Copyright
© The Animal Consortium 2017 

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Abi-Ayad, S, Kestemont, P and Mélard, C 2000. Dynamics of total lipids and fatty acids during embryogenesis and larval development of Eurasian perch (Perca fluviatilis). Fish Physiology and Biochemistry 23, 233243.Google Scholar
Andersson, , Silva, PIM, Steffensen, JF and Höglund, E 2011. Effects of maternal stress coping style on offspring characteristics in rainbow trout (Oncorhynchus mykiss). Hormones and Behavior 60, 699705.Google Scholar
Bell, MV, Henderson, RJ and Sargent, JR 1986. The role of polyunsaturated fatty acids in fish. Comparative Biochemistry and Physiology 83, 711719.Google Scholar
Bobe, J and Labbé, C 2010. Egg and sperm quality in fish. General and Comparative Endocrinology 165, 535548.Google Scholar
Boëchat, IG, Krüger, A, Chaves, RC, Graeber, D and Gücker, B 2014. Land-use impacts on fatty acid profiles of suspended particulate organic matter along a larger tropical river. Science of the Total Environment 482, 6270.Google Scholar
Broach, JS, Ohs, CL and Breen, NE 2017. Protracted volitional spawning of pinfish Lagodon rhomboides and changes in egg quality and fatty-acid composition throughout the spawning season. Journal of Fish Biology, https://doi.org/10.1111/jfb.13381, Published online by The Fisheries Society of the British Isles 26 July 2017.Google Scholar
Brooks, S, Tyler, CR and Sumpter, JP 1997. Quality in fish: what makes a good egg? Reviews in Fish Biology and Fisheries 7, 387416.Google Scholar
Campbell, PM, Pottinger, TG and Sumpter, JP 1994. Preliminary evidence that chronic confinement stress reduces the quality of gametes produced by brown and rainbow trout. Aquaculture 120, 151169.Google Scholar
Czesny, S and Dabrowski, K 1998. The effect of egg fatty acid concentrations on embryo viability in wild and domesticated walleye (Stizostedion vitreum). Aquatic Living Resources 11, 371378.Google Scholar
Czesny, S, Rinchard, J and Dabrowski, K 2005. Intrapopulation variation in egg lipid and fatty acid composition and embryo viability in a naturally spawning walleye population from an inland reservoir. North American Journal of Fisheries Management 25, 122129.Google Scholar
Dabrowski, K, Rinchard, J, Czesny, S and Korzeniowska, M 2015. Effects of dietary levels of PUFA fed to adult yellow perch on the fatty acid composition of eggs and larvae characteristics: new research directions. In Biology and culture of percid fishes (ed. P Kestemont, K Dabrowski and RC Summerfelt), pp. 565586. Springer Verlag, Dordrecht, the Netherlands.Google Scholar
Fernández-Palacios, H, Izquierdo, MS, Robaina, L, Valencia, A, Salhi, M and Vergara, JM 1995. Effect of n-3 HUFA level in broodstock diets on egg quality of gilthead sea bream (Sparus aurata L.). Aquaculture 132, 325337.Google Scholar
Gunasekera, RM, De Silva, SS and Ingram, BA 1999. Early ontogeny-related changes of the fatty acid composition in the Percichthyid fishes trout cod, Maccullochellam acquariensis and Murray cod, M. peeliipeelii . Aquatic Living Resources 12, 219227.Google Scholar
Henrotte, E, Mandiki, RSNM, Prudencio, AT, Vandecan, M, Mélard, C and Kestemont, P 2010. Egg and larval quality, and egg fatty acid composition of Eurasian perch breeders (Perca fluviatilis) fed different dietary DHA/EPA/AA ratios. Aquaculture Research 41, 5361.Google Scholar
Hermelink, B, Wuertz, S, Trubiroha, A, Rennert, B, Kloas, W and Schulz, C 2011. Influence of temperature on puberty and maturation of pikeperch, Sander lucioperca . General and Comparative Endocrinology 172, 282292.Google Scholar
Hermelink, B, Wuertz, S, Rennert, B, Kloas, W and Schulz, C 2013. Temperature control of pikeperch (Sander lucioperca) maturation in recirculating aquaculture systems-induction of puberty and course of gametogenesis. Aquaculture 400, 3645.Google Scholar
Hwang, PP, Wu, SM, Lin, JH and Wu, LS 1992. Cortisol content of eggs and larvae of teleosts. General and Comparative Endocrinology 86, 189196.Google Scholar
Izquierdo, MS, Fernández-Palacios, H and Tacon, AGJ 2001. Effect of broodstock nutrition on reproductive performance of fish. Aquaculture 197, 2542.Google Scholar
Kestemont, P and Henrotte, E 2015. Nutritional requirements and feeding of broodstock and Early life stages of Eurasian perch and pikeperch. In Biology and culture of percid fishes (ed. P Kestemont, K Dabrowski and RC Summerfelt), pp. 539564. Springer Verlag, Dordrecht, the Netherlands.Google Scholar
Khemis, IB, Hamza, N, Messaoud, NB, Rached, SB and M’Hetli, M 2014. Comparative study of pikeperch Sander lucioperca (Percidae; Linnaeus, 1758) eggs and larvae from wild females or from captive females fed chopped marine fish. Fish Physiology and Biochemistry 40, 375384.Google Scholar
Leroy, J, Vanholder, T, Mateusen, B, Christophe, A, Opsomer, G, de Kruif, A, Genicot, G and Van Soom, A 2005. Non-esterified fatty acids in follicular fluid of dairy cows and their effect on developmental capacity of bovine oocytes in vitro. Reproduction 130, 485495.Google Scholar
Lund, I and Steenfeldt, SJ 2011. The effects of dietary long-chain essential fatty acids on growth and stress tolerance in pikeperch larvae (Sander lucioperca L.). Aquaculture Nutrition 17, 191199.Google Scholar
Lund, I, Skov, PV and Hansen, BW 2012. Dietary supplementation of essential fatty acids in larval pikeperch (Sander lucioperca); short and long term effects on stress tolerance and metabolic physiology. Comparative Biochemistry and Physiology 162, 340348.Google Scholar
Mejri, S, Audet, C, Vandenberg, GW, Parrish, CC and Tremblay, R 2014. Biochemical egg quality in a captive walleye (Sander vitreus) broodstock population relative to ovulation timing following hormonal treatment. Aquaculture 431, 99106.Google Scholar
Migaud, H, Bell, G, Cabrita, E, McAndrew, B, Davie, A, Bobe, J, Herraez, MP and Carrillo, M 2013. Gamete quality and broodstock management in temperate fish. Reviews in Aquaculture 5, 194223.Google Scholar
Milla, S, Wang, N, Mandiki, SNM and Kestemont, P 2009. Corticosteroids: friends or foes of teleost fish reproduction? Comparative Biochemistry and Physiology 153, 242251.Google Scholar
Moodie, GEE, Loadman, NL, Wiegand, MD and Mathias, JA 1989. Influence of egg characteristics on survival, growth and feeding in larval walleye (Stizostedion vitreum). Journal of Fisheries and Aquatic Sciences 46, 516521.Google Scholar
Sarameh, SP, Falahatkar, B, Takami, GA and Efatpanah, I 2013. Physiological changes in male and female pikeperch Sander lucioperca (Linnaeus, 1758) subjected to different photoperiods and handling stress during the reproductive season. Fish Physiology and Biochemistry 39, 12531266.Google Scholar
Sargent, JR, Tocher, DR and Bell, JG 2002. The lipids. In Fish nutrition (ed. JE Halver and RW Hardy), pp. 181257. Academic press, San Diego, CA, USA.Google Scholar
Schaefer, FJ, Overton, JL and Wuertz, S 2016. Pikeperch Sander lucioperca egg quality cannot be predicted by total antioxidant capacity and mtDNA fragmentation. Animal Reproduction Science 167, 117124.Google Scholar
Schaefer, FJ 2016. Reproductive management and gamete quality in pikeperch (Sander lucioperca). PhD thesis, Humboldt Universität zu Berlin, Berlin, Germany.Google Scholar
Schaerlinger, B and Żarski, D 2015. Evaluation and improvements of egg and larval QUALITY in percid fishes. In Biology and culture of percid fishes (ed. P Kestemont, K Dabrowski and RC Summerfelt), pp. 193226. Springer Verlag, Dordrecht, the Netherlands.Google Scholar
Schreck, CB, Contreras-Sanchez, W and Fitzpatrick, MS 2001. Effects of stress on fish reproduction, gamete quality, and progeny. Aquaculture 197, 324.Google Scholar
Strand, Å, Magnhagen, C and Alanärä, A 2007. Effects of repeated disturbances on feed intake, growth rates and energy expenditures of juvenile perch, Perca fluviatilis. Aquaculture 265, 163168.Google Scholar
Stratholt, ML, Donaldson, EM and Liley, NR 1997. Stress induced elevation of plasma cortisol in adult female coho salmon (Oncorhynchus kisutch), is reflected in egg cortisol content, but does not appear to affect early development. Aquaculture 158, 141153.Google Scholar
Tocher, DR 2003. Metabolism and functions of lipids and fatty acids in teleost fish. Reviews in Fisheries Science 11, 107184.Google Scholar
Valdebenito, II, Gallegos, PC and Effer, BR 2015. Gamete quality in fish: evaluation parameters and determining factors. Zygote 23, 177197.Google Scholar
Van Anholt, RD, Spanings, EAT, Koven, WM, Nixon, O and Bonga, SEW 2004. Arachidonic acid reduces the stress response of gilthead seabream Sparus aurata L. Journal of Experimental Biology 207, 34193430.Google Scholar
Watanabe, T, Takeuchi, T, Saito, M and Nishimura, K 1984. Effect of low protein-high calory or essential fatty acid deficiency diet on reproduction of rainbow trout. Bulletin of the Japanese Society for the Science of Fish 50, 12071215.Google Scholar
Wiegand, MD 1996. Composition, accumulation and utilization of yolk lipids in teleost fish. Reviews in Fish Biology and Fisheries 6, 259286.Google Scholar
Yang, Q, Zheng, P, Ma, Z, Li, T, Jiang, S and Qin, JG 2015. Molecular cloning and expression analysis of the retinoid X receptor (RXR) gene in golden pompano Trachinotus ovatus fed Artemia nauplii with different enrichments. Fish Physiology and Biochemistry 41, 14491461.Google Scholar
Żarski, D, Horváth, Á, Held, JA and Kucharczyk, D 2015. Artificial reproduction of percid fishes. In Biology and culture of percid fishes (ed. P Kestemont, K Dabrowski and RC Summerfelt), pp. 123162. Springer Verlag, Dordrecht, the Netherlands.Google Scholar