Research Article
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Year 2021, , 87 - 92, 31.12.2021
https://doi.org/10.51756/marlife.1013282

Abstract

References

  • Aktaş, M., Eroldoğan, O. T. & Kumlu, M. (2004). Combined effects of temperature and salinity on egg hatching rate and incubation time of Penaeus semisulcatus (Decapoda: Penaeidae). Israeli Journal of Aquaculture-Bamidgeh, 56(2): 124-128.
  • Aktaş, M. & Çavdar, N. (2012). The combined effects of salinity and temperature on the egg hatching rate, incubation time, and survival until protozoal stages of Metapenaeus monoceros (Fabricius) (Decapoda: Penaeidae). Turkish Journal of Zoology, 36(2): 249-253.
  • Courties, C. (1976). Description des premiers stades larvaires de trios crevettes peneides pechees a Madagascar: Penaeus indicus H. Milne Edwards, Penaeus semisulcatus de Haan, Metapenaeus monoceros (Fabricius). Cahiers Orstom series Oceanographie, 14: 49-70.
  • Deval, M. C., Kaya, Y., Güven, O., Gökoğlu, M. & Froglia, C. (2010). An unexpected find of the western Atlantic shrimp, Farfantepenaeus aztecus (Ives, 1891) (Decapoda, Penaeidae) in Antalya Bay, eastern Mediterranean Sea. Crustaceana, 83: 1531-1537.
  • FAO, (2020). The state of world fisheries and aquaculture 2020: Sustainability in action. Rome. 244 p.
  • Gandy, R. L. (2004). Investigations into the reproductive performance and larval rearing of the Brown shrimp, Farfantepenaeus aztecus, using closed recirculating systems. Doctoral dissertation, Texas A&M University.
  • Gökoğlu, M. & Özvarol, Y. (2013). New Mediterranean marine biodiversity records Biogeographic expansion of Farfantepenaeus aztecus (Ives, 1891) (Decapoda: Penaeidae) in the Eastern Mediterranean Sea. Mediterranean Marine Science, 14: 475-476.
  • Kapiris, K., Apostolidis, C., Baldacconi, R., Başusta, N., Bilecenoğlu, M., Bitar, G., Bobori, D.C., Boyaci. Y.Ö., Dimitriadis, C., Djurović, M., Dulcic, J., Durucan, F., Gerovasileiou, V., Gökoğlu, M., Koutsoubas, D., Lefkaditou, E., Lipej, L., Marković, O., Mavrič, B., Özvarol, Y., Pesic, V., Petriki, O., Siapatis, A., Sini, M., Tibullo, D. & Tiralongo, F. (2014). New Mediterranean marine biodiversity records. Mediterranean Marine Science, 15: 198-212.
  • Kjøsrvik, E., Mangor-Jensen, A. & Holmefjord, I. (1990). Egg quality in fishes. In: Blaxter J.H.S. and Southward A.J. (eds.), Advance in Marine Biology, Vol. 26. Academic Press, pp. 71–113.
  • Lester, L. J. & Pante, M. J. R. (1992). Penaeid temperature and salinity responses. In: Marine Shrimp Culture: Principle and Practices (eds. A.W. Fast and L.J. Lester), Elsevier, Amsterdam, pp. 515- 535.
  • Minos, G., Kokokiris, L., Imsiridou, A., Karachle, P. & Kapiris, K. (2015). Notes on the distribution and biology of northern brown shrimp Farfantepenaeus aztecus (Ives, 1891) in the Eastern Mediterranean. Turkish Journal of Zoology, 39: 1-7.
  • Nisa, Z. & Ahmet, M. (2000). Hatching and larval survival of important penaeid shrimps of Pakistan in different salinities. Pakistan Journal of Zoology, 32: 139-143.
  • Palacios, E., Ibarra, A. M., Ramirez, J. L., Portillo, G. & Racotta. I. S. (1998). Biochemical composition of eggs and nauplii in white pacific shrimp, Penaeus vannamei (Boone), in relation to the physiological condition of spawners in a commercial hatchery. Aquaculture Research ,29: 183-189.
  • Preston, N. (1985). The effects of temperature and salinity on survival and growth of larval Penaeus plebejus, Metapenaeus macleayi and M. bennettae. In: 2nd Australian Natl. Prawn Seminar (eds. P.C. Rothlisberg, B.J. Hill and D.J. Staples), NPS2, Cleveland, Australia, pp. 31-40.
  • Primavera, J. H. (1985). A review of maturation and reproduction in closed thelycum Penaeids. Proceedings of the First International Conference on the Culture of Penaeid Prawns/Shrimps, 47-64.
  • Regunathan, C. (2008). Variation in reproductive performance and egg quality between wild and pond-reared Indian White Shrimp, Fenneropenaeus indicus, Broodstock. Journal of Applied Aquaculture, 20(1): 1-17.
  • Simmons, E. G. (1957). An ecological survey of the upper Laguna Madre of Texas. Publication of the Institute of Marine Science of the University of Texas, 4: 156-200.
  • Soud, P. & Davis, D. A. (2003). Salinity tolerance of Brown Shrimp Farfantepenaeus aztecus as it relates to post larval growth and juvenile survival, distribution and growth in estuaries. Estuaries, 26(4): 970-974.
  • Tseng, W. Y. & Cheng, W. W. (1981). The artificial propagation and culture of bear shrimp, Penaeus semisulcatus de Hann, in Hong Kong. Journal of the World Mariculture Society, 12(2): 260-281.
  • Zein-Eldin, Z. P. & Renaud, M. L. (1986). Inshore environmental effects on brown shrimp, Penaeus aztecus, and white shrimp, P. setiferus, populations in coastal waters, particularly of Texas. Marine Fisheries Review, 48: 9-19.
  • Zacharia S. & Kakati, V. S. (2004). Optimal salinity and temperature for early developmental stages of Penaeus merguiensis De man. Aquaculture, 232: 373-382.

The effect of salinity and temperature on egg hatching rate, hatching time and larval activity of Farfantepenaeus aztecus (Ives, 1891) (Decapoda: Penaeidae)

Year 2021, , 87 - 92, 31.12.2021
https://doi.org/10.51756/marlife.1013282

Abstract

This study was conducted to determine the optimum temperature and salinity for the hatching rate, hatching time of eggs and larval activity of Farfantepenaeus aztecus (Ives, 1891). For this purpose, F. aztecus, which was caught from nature in the 4th gonad stage and were spawned on the same night in controlled laboratory conditions. The eggs were stocked in 2-l round bottom glass flasks and received one of nine temperature (24, 28 and 32°C) and salinity (30, 35 and 40 ppt) combinations as 50 eggs per liter after determining the fertility rate of the eggs. Although eggs hatched in all salinity and temperature combinations, water temperature, salinity and interaction had significant effects on hatching rate, hatching time and larval activity (P<0.05). Considering only salinity, the best hatching ratio was found at 35 ppt (48.44%), 40 ppt (47.89%) and the lowest hatching rate was found at 30 ppt (34.77%, P<0.05). It was found that the best hatching ratios were at 28°C (52.22%), at 32°C (48.33%) and followed by the eggs incubated 24°C (30.55%, P<0.05). The incubation time was shortened due to the increase in water temperature and changed between 11.40-17.10 hours. It was determined that the activities of the larvae incubated at lowest water temperature (24°C) and at 30 ppt were weaker than those incubated at 28°C and 35- 40 ppt salinities. The results show that 28-32°C water temperature and sea salinity slightly less than the salinity of the Mediterranean Sea (38.5 ppt) are optimal for the incubation eggs and for the production of high quality nauplii of F. aztecus found in the Northeastern Mediterranean.

Thanks

This article is part of the first author's master thesis. The authors thank Dr. Yavuz Mazlum for his data analysis and valuable suggestions for this manuscript.

References

  • Aktaş, M., Eroldoğan, O. T. & Kumlu, M. (2004). Combined effects of temperature and salinity on egg hatching rate and incubation time of Penaeus semisulcatus (Decapoda: Penaeidae). Israeli Journal of Aquaculture-Bamidgeh, 56(2): 124-128.
  • Aktaş, M. & Çavdar, N. (2012). The combined effects of salinity and temperature on the egg hatching rate, incubation time, and survival until protozoal stages of Metapenaeus monoceros (Fabricius) (Decapoda: Penaeidae). Turkish Journal of Zoology, 36(2): 249-253.
  • Courties, C. (1976). Description des premiers stades larvaires de trios crevettes peneides pechees a Madagascar: Penaeus indicus H. Milne Edwards, Penaeus semisulcatus de Haan, Metapenaeus monoceros (Fabricius). Cahiers Orstom series Oceanographie, 14: 49-70.
  • Deval, M. C., Kaya, Y., Güven, O., Gökoğlu, M. & Froglia, C. (2010). An unexpected find of the western Atlantic shrimp, Farfantepenaeus aztecus (Ives, 1891) (Decapoda, Penaeidae) in Antalya Bay, eastern Mediterranean Sea. Crustaceana, 83: 1531-1537.
  • FAO, (2020). The state of world fisheries and aquaculture 2020: Sustainability in action. Rome. 244 p.
  • Gandy, R. L. (2004). Investigations into the reproductive performance and larval rearing of the Brown shrimp, Farfantepenaeus aztecus, using closed recirculating systems. Doctoral dissertation, Texas A&M University.
  • Gökoğlu, M. & Özvarol, Y. (2013). New Mediterranean marine biodiversity records Biogeographic expansion of Farfantepenaeus aztecus (Ives, 1891) (Decapoda: Penaeidae) in the Eastern Mediterranean Sea. Mediterranean Marine Science, 14: 475-476.
  • Kapiris, K., Apostolidis, C., Baldacconi, R., Başusta, N., Bilecenoğlu, M., Bitar, G., Bobori, D.C., Boyaci. Y.Ö., Dimitriadis, C., Djurović, M., Dulcic, J., Durucan, F., Gerovasileiou, V., Gökoğlu, M., Koutsoubas, D., Lefkaditou, E., Lipej, L., Marković, O., Mavrič, B., Özvarol, Y., Pesic, V., Petriki, O., Siapatis, A., Sini, M., Tibullo, D. & Tiralongo, F. (2014). New Mediterranean marine biodiversity records. Mediterranean Marine Science, 15: 198-212.
  • Kjøsrvik, E., Mangor-Jensen, A. & Holmefjord, I. (1990). Egg quality in fishes. In: Blaxter J.H.S. and Southward A.J. (eds.), Advance in Marine Biology, Vol. 26. Academic Press, pp. 71–113.
  • Lester, L. J. & Pante, M. J. R. (1992). Penaeid temperature and salinity responses. In: Marine Shrimp Culture: Principle and Practices (eds. A.W. Fast and L.J. Lester), Elsevier, Amsterdam, pp. 515- 535.
  • Minos, G., Kokokiris, L., Imsiridou, A., Karachle, P. & Kapiris, K. (2015). Notes on the distribution and biology of northern brown shrimp Farfantepenaeus aztecus (Ives, 1891) in the Eastern Mediterranean. Turkish Journal of Zoology, 39: 1-7.
  • Nisa, Z. & Ahmet, M. (2000). Hatching and larval survival of important penaeid shrimps of Pakistan in different salinities. Pakistan Journal of Zoology, 32: 139-143.
  • Palacios, E., Ibarra, A. M., Ramirez, J. L., Portillo, G. & Racotta. I. S. (1998). Biochemical composition of eggs and nauplii in white pacific shrimp, Penaeus vannamei (Boone), in relation to the physiological condition of spawners in a commercial hatchery. Aquaculture Research ,29: 183-189.
  • Preston, N. (1985). The effects of temperature and salinity on survival and growth of larval Penaeus plebejus, Metapenaeus macleayi and M. bennettae. In: 2nd Australian Natl. Prawn Seminar (eds. P.C. Rothlisberg, B.J. Hill and D.J. Staples), NPS2, Cleveland, Australia, pp. 31-40.
  • Primavera, J. H. (1985). A review of maturation and reproduction in closed thelycum Penaeids. Proceedings of the First International Conference on the Culture of Penaeid Prawns/Shrimps, 47-64.
  • Regunathan, C. (2008). Variation in reproductive performance and egg quality between wild and pond-reared Indian White Shrimp, Fenneropenaeus indicus, Broodstock. Journal of Applied Aquaculture, 20(1): 1-17.
  • Simmons, E. G. (1957). An ecological survey of the upper Laguna Madre of Texas. Publication of the Institute of Marine Science of the University of Texas, 4: 156-200.
  • Soud, P. & Davis, D. A. (2003). Salinity tolerance of Brown Shrimp Farfantepenaeus aztecus as it relates to post larval growth and juvenile survival, distribution and growth in estuaries. Estuaries, 26(4): 970-974.
  • Tseng, W. Y. & Cheng, W. W. (1981). The artificial propagation and culture of bear shrimp, Penaeus semisulcatus de Hann, in Hong Kong. Journal of the World Mariculture Society, 12(2): 260-281.
  • Zein-Eldin, Z. P. & Renaud, M. L. (1986). Inshore environmental effects on brown shrimp, Penaeus aztecus, and white shrimp, P. setiferus, populations in coastal waters, particularly of Texas. Marine Fisheries Review, 48: 9-19.
  • Zacharia S. & Kakati, V. S. (2004). Optimal salinity and temperature for early developmental stages of Penaeus merguiensis De man. Aquaculture, 232: 373-382.
There are 21 citations in total.

Details

Primary Language English
Subjects Hydrobiology
Journal Section Research Articles
Authors

Dilber Çolakoğlu Durmuş 0000-0003-0708-0309

Mevlüt Aktaş 0000-0002-7851-0014

Publication Date December 31, 2021
Submission Date October 22, 2021
Acceptance Date November 25, 2021
Published in Issue Year 2021

Cite

APA Çolakoğlu Durmuş, D., & Aktaş, M. (2021). The effect of salinity and temperature on egg hatching rate, hatching time and larval activity of Farfantepenaeus aztecus (Ives, 1891) (Decapoda: Penaeidae). Marine and Life Sciences, 3(2), 87-92. https://doi.org/10.51756/marlife.1013282

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