The Effect of Day Length and Lunar Phases on the Spawning Activity in the Nile Tilapia Oreochromis niloticus

  • Kwon, Joon-Yeong (Dept. of Aquatic Life Medical Sciences, Sunmoon University) ;
  • Kim, Jung-Hyun (Dept. of Aquatic Life Medical Sciences, Sunmoon University) ;
  • Kim, Bo-Kyong (Dept. of Aquatic Life Medical Sciences, Sunmoon University)
  • 투고 : 2009.02.03
  • 심사 : 2010.03.04
  • 발행 : 2010.03.31

초록

Nile tilapia (Oreochromis niloticus) are mouth-brooders so that the females holding eggs in their mouth sacrifice their somatic growth for reproduction. For this reason, artificial control of reproduction for the culture of this species has been of interest. Manipulation of photoperiod is an emerging technique for such purpose, but little information is available to establish appropriate photoperiod regime. To obtain necessary basic information, sexually mature females were individually accommodated to glass aquarium, and the spawning activity of these females were monitored for two years under natural photoperiod regime. Female tilapia spawned most frequently on March, April and May when the day length gradually increased from 11 hours to 14 hours and least frequently on September, October, November and December when the day length gradually decreased from 13 hours to less than 10 hours in the first year. The decrease of spawning frequency as day length decreased was also observed in the second year, although the increase of spawning frequency as day length increased was less clear. Spawning of female tilapia was less active when the night was dark due to the disappearance of moonlight (Dark Phase), compared to the Phase of Getting Lighter, Light Phase and Phase of Getting Darker. Results from this study suggest that long day length, particularly increasing phase, is favoured for active spawning of Nile tilapia, and that this species, as a tropical fish species, may utilize changing lunar phases as a secondary environmental cue for reproduction.

키워드

참고문헌

  1. Biswas AK, Morita T, Yoshizaki G, Maita M, Takeuchi T (2005) Control of reproduction in Nile tilapia Oreochromis niloticus (L.) by photoperiod manipulation. Aquaculture 243:229-239. https://doi.org/10.1016/j.aquaculture.2004.10.008
  2. Boeuf G, Le Bail PL (1999) Does light have an influence on fish growth? Aquaculture 177:129-152. https://doi.org/10.1016/S0044-8486(99)00074-5
  3. Bromage N, Porter M, Randall C (2001) Environmental regulation of maturation in farmed finfish with special reference to the role of photoperiod and melatonin. Aquaculture 197:63-69. https://doi.org/10.1016/S0044-8486(01)00583-X
  4. Campos-Mendoza A, McAndrew BJ, Coward K, Bromage N (2004) Reproductive response of Nile tilapia (Oreochromis niloticus) to photoperiod manipulation; effects on spawning periodicity, fecundity and egg size. Aquaculture 231: 299-313. https://doi.org/10.1016/j.aquaculture.2003.10.023
  5. Gines A, Afonso JM, Arguello A, Zamorano MJ, Lopez JL (2004) The effects of long-day photoperiod on growth, body composition and skin colour in immature gilthead sea bream (Sparus aurata L.). Aquaculture Research 35:1207-1212. https://doi.org/10.1111/j.1365-2109.2004.01126.x
  6. Kwon JY, Haghpanah V, Kogson-Hurtado LM, McAndrew BJ, Penman DJ (2000) Masculinization of genetic female Nile tilapia (Oreochromis niloticus) by dietary administration of an aromatase inhibitor during sexual differentiation. J Exp Zool 287:46-53. https://doi.org/10.1002/1097-010X(20000615)287:1<46::AID-JEZ6>3.0.CO;2-X
  7. Kwon JY, McAndrew BJ, Penman DJ (2002). Treatment with an aromatase inhibitor suppresses high-temperature feminization of genetic male (YY) Nile tilapia. J Fish Biol 60:625-636. https://doi.org/10.1111/j.1095-8649.2002.tb01689.x
  8. Longalong FM, Eknath AE, Bentsen HB (1999) Response to bidirectional selection for frequency of early maturing females in Nile tilapia (Oreochromis niloticus). Aquaculture 178:13-25. https://doi.org/10.1016/S0044-8486(99)00132-5
  9. Martinez-Chavez CC, Migaud H (2009) Retinal light input is required to sustain plasma melatonin rhythms in Nile tilapia Oreochromis niloticus niloticus. Brain Research 1269:61-67. https://doi.org/10.1016/j.brainres.2009.03.009
  10. McAndrew BJ (1993) Sex control in tilapiines. In: Muir JF, Robert RJ (eds.), Recent Advances in Aquaculture IV, Blackwell Science, New York, pp. 87-98.
  11. Oppedal F, Taranger GL, Juell JE, Hansen T (1999) Growth, osmoregulation and sexual maturation of under yearing Atlantic salmon (Salmo salar) exposed to different intensities of continuous light in sea cages. Aquaculture Research 30:491-499. https://doi.org/10.1046/j.1365-2109.1999.00362.x
  12. Rad F, Bozao?u S, G??ara SE, Karahan A, Kurt G (2006) Effects of different long-day photoperiods on somatic growth and gonadal development in Nile tilapia (Oreochromis niloticus L.). Aquaculture 255:292-300. https://doi.org/10.1016/j.aquaculture.2005.11.028
  13. Randall C, North B, Futter W, Porter M, Bromage N (2001) Photoperiod effects on reproduction and growth in rainbow trout. Trout News 32:12-16.
  14. Ridha MT, Cruz EM (2000) Effect of light intensity and photoperiod on Mile tilapia Oreochromis niloticus seed production. Aquaculture Research 31:609-617. https://doi.org/10.1046/j.1365-2109.2000.00481.x
  15. Ridha MT, Cruz EM, Al-Ameeri AA, Al-Ahmed AA (1998) Effects of controlling temperature and light duration on seed production in tilapia, Orechromis spilurus (Gunter). Aquaculture Research 29:403-410.
  16. Rodriguez L, Zanuy S, Carrillo M (2001) Influence of day length on the age at first maturity and somatic growth in male sea bass (Dicentrarchus labrax L.). Aquaculture 196:159-175. https://doi.org/10.1016/S0044-8486(00)00555-X
  17. Simensen LM, Jonassen TM, Imsland AK, Stefansson SO (2000) Photoperiod regulation of growth of juvenile Atlantic halibut (Hippoglossus hippoglossus). Aquaculture 190:119-128. https://doi.org/10.1016/S0044-8486(00)00397-5
  18. Takemura A, Rahman MR, Nakamura S, Park YJ, Takano K (2004) Lunar cycles and reproductive activity in reef fishes with particular attention to rabbitfishes. Fish and Fisheries 5:317-328. https://doi.org/10.1111/j.1467-2679.2004.00164.x
  19. Thresher, R.E. (1984) Reproduction in Reef Fishes. T.F.H. Publications, Neptune City, NJ.