Sex determination, mating behavior and spawning frequency of captive wild blueband goby broodstocks, Valenciennea strigata
Keywords:
Blueband goby, mating behavior, sex determination, spawning frequency, Valenciennea strigataAbstract
This research was to examine the sex determination, mating behavior, and spawning frequency of captive wild blueband goby broodstocks, Valenciennea strigata, under laboratory conditions. The experiment was conducted over a 12 months period in a hatchery at Bangsaen Institute of Marine Science for a period of Chon Buri province, Thailand. Eight pairs of blueband goby broodstocks, derived from Chatuchak Market, Bangkok, were maintained in a biological recirculating system with tanks measuring 15 x 24 x 15 inches (70 liters of seawater). They were fed pelleted feed twice a day and supplemented with adults Artemia once a day for the duration of the study.
Results revealed that the broodstocks had total weight ranging from 2.7 g to 19.4 g (average 5.8 ± 3.8 g) and total lengths between 7.1 and 13.8 cm (average 8.7 ± 1.5 cm) (n = 16). Sex determination showed that sex can be differentiated by the genital papilla: males have small sex polyps, and the females have rounded sex lobes, along with a more open anus compared to males. These secondary sexual characteristics may be helpful in sexing blueband goby.
Blueband gobies use external fertilization with breeding behaviour occurred in the evening after sunset and taking about 45 minutes to complete the laying process. The eggs were adhesive and oval-shaped, with sizes ranging from 1.0 to 1.1 mm in length and 0.3 mm in width. The spawning occurred every 10 to 12 days (10 ± 0.89 days) (n = 7), and the number of eggs ranged from 3,604 to 34,000 eggs (n = 5). The embryonic period lasted 56 hours and 30 minutes after fertilization. This study provided fundamental data that can serve as a guideline for raising blueband goby and other marine gobiidae.
References
Arakawa, T., Kanno, Y., Akiyama, N., Kitano, T., Nakatsuji, N., & Nakatsuji, T. (1999). Stages of embryonic development of the ice goby (Shiro-uo), Leucopsarion petersii. Zoological Science, 16, 761–773. https://doi.org/10.2108/zsj.16.761
Boulenger, G. A. (1916). Catalogue of the freshwater fishes of Africa (4th ed.). Trustees of the British Museum (Natural History).
Gill, T. N. (1860). Conspectus piscium in expeditione and Oceanum Pacifcum septemtrionalem. Sicydinae. Proceedings of the Pennsylvania Academy of Science, 12, 101–102.
Gopakumar, G., Maghu, K., Madhu, R., & Anil, M. K. (2011). Marine ornamental fish culture – Package of practices. Niseema Printers and Publishers.
Günther, A. C. L. G. (1880). Report on the shore fishes procured during the voyage of H.M.S. Challenger in the years 1873–1876. Biodiversity Heritage Library.
Harding, J. A., Almany, G. R., Houck, L. D., & Hixon, M. A. (2003). Experimental analysis of monogamy in the Caribbean cleaner goby, Gobiosoma evelynae. Animal Behavior, 64, 1–11. https://doi.org/10.1006/anbe.2003.2144
Kannan, K., Sureshkumar, K., Ranjith, L., Joshi, K. K., Madan, M. S., & John, S. (2013). First record of the two-stripe goby, Valenciennea helsdingenii (Gobiidae, Gobiiformes) from the southeast coast of India. ZooKeys, 323, 91–97. https://doi.org/10.3897/zookeys.323.5440
Lau, E. Y. K. (1973). Dimorphism and speciation in the Hawaiian freshwater goby genus Lentipes [Honors thesis, University of Hawaii].
Maciolek, J. A. (1977). Taxonomic status, biology, and distribution of Hawaiian Lentipes, a diadromous goby. Pacific Science, 31, 355–362.
Molina, L., & Segade, A. (2011). Aquaculture as a potential support of marine aquarium fish trade sustainability. WIT Transactions on Ecology and the Environment, 148, 15–25. https://doi.org/10.2495/RAV110021
Pouil, S., Tlusty, M. C., Rhyne, A. L., & Metian, M. (2020). Aquaculture of marine ornamental fish: Overview of the production trends and the role of academia in research progress. Aquaculture, 12, 1217–1230. https://doi.org/10.1111/raq.12381
Robert, H. R. (1997). The natural history of a monogamous coral-reef fish, Valenciennea strigata (Gobiidae): 2. Behavior, mate fidelity, and reproductive success. Journal of Environmental Biology of Fishes, 49(2), 247–257. https://doi.org/10.1023/A:1007320708862
Ruiz, J. M. C. (2012). Cryptocentrus cinctus. Practical experience in maintenance and reproduction. Retrieved from http://aquaticnotes.com/content/pub/EN/cryptocentrus.pdf
Suzuki, T. (2016). Valenciennea yanoi, a new gobiid fish from the Ryukyu Islands, Japan (Teleostei: Gobiidae). Ocean Science Foundation, 21, 1–9. https://doi.org/10.5281/zenodo.51211
Teskong, C., Khumserani, T., Khundee, P., & Lungoon, N. (2019). Trading data (species composition, volume, and value) of Gobiidae at marine ornamental shops in the area of Jatujak Weekend Market, Bangkok Province. Khon Kaen Agriculture Journal, 47(1), 1181–1186.
Wabnitz, C., Taylor, M., Green, E., & Razak, T. (2003). From ocean to aquarium: The global trade in marine ornamental species. UNEP-WCMC.
Downloads
Published
How to Cite
Issue
Section
License
Copyright (c) 2025 Food Agricultural Sciences and Technology

This work is licensed under a Creative Commons Attribution-NoDerivatives 4.0 International License.




