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DETECTION OF THE EXTERNAL SEX SPECIFIC FEATURES IN THE STRUCTURE OF CORIUM DERIVATIVES OF LARVAE AND JUVENILES OF STERLET ACIPENSER RUTHENUS

Abstract

Only females are used in technology of caviar aquaculture, and the males shall be rejected as soon as possible. It is believed that sturgeons have no clearly defined external morphological sex character. Because of the dark color of most sturgeons, the external morphological character, the structure and form of which are sex-dependent, have not been noticed earlier. The aim of our work was to study the morphological structure of the derivatives of the corium (dorsal scutes) of different-age sterlet and to identify its sex-dependent structure. The object of this study was the broodstock of 3-year sterlet of the Volga population, with the gonads of the second stage of maturity, as well as the three-month larva and year-old juvenile sterlet. Cultivation was carried out in the re-circulating aquaculture system at an average water temperature of 16 ± 2  °C. Wintering was not used. We were the first in the practice of ichthyology and aquaculture who found that dorsal scutes of sterlet maturing had significant sex-dependent morphological differences. To assess the morphological structure of the dorsal scutes, it was proposed to define two groups of indicators characterizing the scutes shape, as well as the structure of the cusps of scutes. We found that dorsal scutes of males are more extended in width and have a flattened shape. Dorsal scutes of males have long and thin cusps, the number of which is larger than that of females. For the first time it was found that the established dependence on the structure of dorsal scutes of sterlet is saved as in juveniles with an average length of 24.8  ±   1.5 cm and larvae with an average length of 70.3  ± 3.6 mm. Our results form a methodological basis for global aquaculture practice in effort to develop systems of early and very early sex identification of all Acipenseridae, including the early stages of ontogeny.

About the Author

N. V. Barulin
Belarusian State Agricultural Academy
Belarus
Ph. D. (Agrarian), Assistant Professor, Head of the Department


References

1. Barulin N. V. Serum enzyme response of captive sturgeon brookstock Acipenser baerii Brandt 1869 females and two hybrids (bester = female Huso huso Linnaeus, 1758 × male Acipenser ruthenus Linneaus, 1758, and RsSs = A. gueldenstaedtii Brandt 1833 × A. baerii Brandt 1869) to hormonal stimulation for spawning induction. Journal of Applied Ichthyology, 2015, vol. 31, pp. 2–6. doi.org/10.1111/jai.12898.

2. Zhivotovsky  L. A., Kim  H. Y. Morphological markers of sex in pink salmon Oncorhynchus gorbuscha (Salmonidae). Journal of Ichthyology, 2015, vol. 55, no. 1, pp. 131–133. doi.org/10.1134/s003294521501021x.

3. Falahatkar B., Poursaeid S. Gender Identifification in Great Sturgeon (Huso huso) Using Morphology, Sex Steroids, Histology and Endoscopy. Anatomia, Histologia, Embryologia. 2014, vol. 43, no. 2, pp. 81–89. doi.org/10.1111/ahe.12049.

4. Chebanov M. S., Galich E. V. Sturgeon hatchery manual. FAO Fisheries and Aquaculture, 2010, Technical Paper no. 558, XXXII. 303 p.

5. Hurvitz A., Jackson K., Degani G., Levavi-Sivan B. Use of endoscopy for gender and ovarian stage determinations in Russian sturgeon (Acipenser gueldenstaedtii) grown in aquaculture. Aquaculture, 2007, vol. 270, pp. 158–166. doi.org/10.1016/j.aquaculture.2007.05.020.

6. Webb M. A. H., Feist G. W., Foster E. P., Schreck C. B., Fitzpatrick M. S. Potential classification of sex and stage of gonadal maturity of wild white sturgeon using blood plasma indicators. Transactions of the American fisheries society, 2002, vol. 131, no. 1, pp. 132–142. doi.org/10.1577/1548-8659(2002)131%3C0132:pcosas%3E2.0.co;2.

7. Hao Du, Xiaoyan Zhang, Xiaoqian Leng, Shuhuan Zhang, Jiang Luo, Zhigang Liu, Xingmei Qiao, Boyd Kynard, Qiwei Wei. Gender and gonadal maturity stage identification of captive Chinese sturgeon, Acipenser sinensis, using ultrasound imagery and sex steroids. General and Comparative Endocrinology, 2016. doi.org/10.1016/j.ygcen.2016.08.004.

8. Vizziano-Cantonnet D., Landro S., Lasalle A., Martínez A., Mazzoni T. S., Quagio-Grassiotto I. Identification of the Molecular Sex-Differentiation Period in the Siberian Sturgeon. Molecular Reproduction and Development, 2016, vol. 83, no. 1, pp. 19–36. doi.org/10.1002/mrd.22589.

9. Lu X.,   Webb M., Talbott M., Van Eenennaam J., Palumbo A., Linares-Casenave J., Doroshov S., Struffenegger P., Rasco B. Distinguishing ovarian maturity of farmed white sturgeon (Acipenser transmontanus) by Fourier transform infrared spectroscopy: a potential tool for caviar production management. Journal of Agricultural and  Food  Chemistry, 2010, vol. 58, no. 7, pp. 4056–4064. doi.org/10.1021/jf9038502.

10. The R Project for Statistical Computing. Vienna, Austria, 2016. Available at: https://www.R-project.org (accessed 21 November 2016).

11. Wuertz S., Reiser S., Gessner J., Kirschbaum F. Morphological Distinction Between Juvenile Stages of the European Sturgeon Acipenser sturio and the Atlantic Sturgeon Acipenser oxyrinchus. Biology and Conservation of the European Sturgeon Acipenser sturio L. 1758, 2011, pp. 53–64. doi.org/10.1007/978-3-642-20611-5_�4.

12. Thieren E., Wouters W., Van Neer W. Guide for the identification of archaeological sea sturgeon (Acipenser sturio and A. oxyrinchus) remains. Cybium, 2015, vol. 39, no. 3, pp. 175–192.

13. Chiotti J. A., Boase J. C., Hondorp D. W., Briggs A. S. Assigning Sex and Reproductive Stage to Adult Lake Sturgeon using Ultrasonography and Common Morphological Measurements. North American Journal of Fisheries Management, 2016, vol. 36, no. 1, pp. 21–29. doi.org/10.1080/02755947.2015.1103823.

14. Mal’tsev A. V., Merkulov Ya. G. A biometric method for determining the sex of acipenserids, including the Russian sturgeon Acipenser gueldenstaedtii (Acipenseridae) of the Azov Population. Journal of Ichthyology, 2016, vol. 46, no. 6, pp. 460–464. https://doi.org/10.1134/s0032945206060075.

15. Vecsei P., Litvak M. K., Noakes D. L. G., Rien T., Hochleithner M. A noninvasive technique for determining sex of live adult North American sturgeons. Environmental Biology of  Fishes, 2003, vol. 68, no. 4, pp. 333–338. doi.org/10.1023/b:ebfi.0000005732.98047.f3.


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ISSN 1561-8323 (Print)
ISSN 2524-2431 (Online)