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Behavioral analysis of rock bream Oplegnathus fasciatus reveals a strong attraction potential for sea urchin extracts

  • Duminda, S.K. Tilan Chamara (Department of Fisheries Biology, Pukyong National University) ;
  • Kim, Yeo-Reum (Department of Fisheries Biology, Pukyong National University) ;
  • Kim, Jong-Myoung (Department of Fisheries Biology, Pukyong National University)
  • Received : 2020.11.30
  • Accepted : 2020.12.17
  • Published : 2021.01.31

Abstract

Monitoring fish movement is important to understand how physiology adapts to environmental change. To explore the applicability of a video tracking system for determining if chemical cues attract or repel aquatic animals, the movement patterns of rock bream, Oplegnathus fasciatus, were analyzed upon exposure to various materials, including extracts of sea urchin, rock worm, bait worm, krill, barley kernel, and commercial fish feed. Pellets were prepared by mixing freeze-dried tissues with a cellulose and corn flour mixture. Behavioral analysis was carried out with five fish that had been acclimated in the adaptation zone of a Y-shaped tank. Preference toward chemical cues was quantified by assessing the frequency rock bream were observed in a discrete zone around the test material located at the end of each arm and the duration each fish stayed in each zone. The analysis of fish movement upon exposure to commercial feed and barley kernel at each end, respectively, indicated a clear preference toward the feed relative to the barley kernel. Movement responses were further tested with pellets containing extracts of sea urchin, one of the species collected on a large scale, and other materials including krill and worms. A stronger preference toward sea urchin (100%) was observed based on the duration of stay in the test zone, compared to krill (90.1 ± 44.2%), bait worm (81.1 ± 39.1%), rock worm (73.7 ± 28.9%), and barley (63.9 ± 25.9%), under the conditions tested. A detailed comparison of rock bream movements toward each material revealed significant differences in frequency and duration, respectively, between pairs of test materials including krill (74 ± 29.8 and 375.6 ± 118.9) vs. rock worm (41.5 ± 18.7 and 160.2 ± 42.6), krill (86.3 ± 22.9 and 477.1 ± 84) vs. bait worm (36.2 ± 5.5 and 166.1 ± 50.7), and rock worm (45.9 ± 26.2 and 213.7 ± 100.1) vs. bait worm (34.6 ± 21.7 and 159.5 ± 98.5). Rock bream exhibited preference for the test materials in the following order: commercial fish feed > sea urchin > krill > rock worm > bait worm > barley. The results suggest a higher potency of sea urchin extract as a rock bream fishing bait compared to the other materials that are used as commercial bait.

Keywords

Acknowledgement

This work was supported by a Research Grant of Pukyong National University (2019 year).

References

  1. Agatsuma Y. Ecology of Strongylocentrotus nudus. In: Lawrence JM, editor. Edible sea urchins: biology and ecology. 2nd ed. Amsterdam, Nederland: Elsevier Science; 2007. p.443-57.
  2. Alos J, Arlinghaus R, Palmer M, March D, Alvarez I. The influence of type of natural bait on fish catches and hooking location in a mixed-species marine recreational fishery, with implications for management. Fish Res. 2009;97:270-7. https://doi.org/10.1016/j.fishres.2009.03.003
  3. Arimoto T. Fish behaviour approach for improving trawl gear selectivity: In: Proceeding of the Regional Workshop on Responsible Fishing; 1997; Bangkok, Thailand. p.251-65.
  4. Atema J. Chemical senses, chemical signals and feeding behavior in fishes. In: Bardach JE, Magnuson JJ, May RC, Reinhart JM, editors. Fish behavior and its use in the capture and culture of fishes. Pulau Pinang, Philippines: International Center for Living Aquatic Resources Management; 1980. p.57-101.
  5. Braubach OR, Wyeth RC, Murray A, Fine A, Roger PC. A simple and effective method to condition olfactory behaviors in groups of zebrafish. In: Kalueff AV, Cachat M, editors. Zebrafish neurobehavioral protocols. New York, NY: Humana Press; 2011. p.85-97.
  6. Broadhurst MK, Hazin FHV. Influences of type and orientation of bait on catches of swordfish (Xiphias gladius) and other species in an artisanal sub-surface longline fishery off northeastern Brazil. Fish Res. 2001;53:169-79. https://doi.org/10.1016/S0165-7836(00)00297-6
  7. Carr WES, Derby CD. Chemically stimulated feeding behavior in marine animals. J Chem Ecol. 1986;12:989-1011. https://doi.org/10.1007/BF01638992
  8. Duminda SKTC. Behavior analysis of sea urchin Strongylocentrotus nudus and rock bream Oplegnathus fasciatus for identifying chemical cues eliciting attractant/repellant responses [M.S. Thesis]. Busan: Pukyong National University; 2020.
  9. Elkins A, Barrow R, Rochfort S. Carp chemical sensing and the potential of natural environmental attractants for control of carp: a review. Environ Chem. 2009;6:357-68. https://doi.org/10.1071/EN09032
  10. Firestein S. How the olfactory system makes sense of scents. Nature. 2001;413:211-8. https://doi.org/10.1038/35093026
  11. Goh Y, Tamura T. Effect of amino acids on the feeding behaviour in red sea bream. Comp Biochem Physiol C Comp Pharmacol. 1980;66:225-9. https://doi.org/10.1016/0306-4492(80)90131-8
  12. Jang JC, Chung JK, Hur YS, Song JH, Kim JM. Behavioral monitoring system for mud shrimp Upogebia major and the photoresponse to illumination with different wavelength LEDs. Korean J Fish Aquat Sci. 2017;50:413-20. https://doi.org/10.5657/KFAS.2017.0413
  13. Jang JC, Choi MJ, Yang YS, Lee HB, Yu YM, Kim JM. Dim-light photoreceptor of chub mackerel Scomber japonicus and the photoresponse upon illumination with LEDs of different wavelengths. Fish Physiol Biochem. 2016;42:1015-25. https://doi.org/10.1007/s10695-015-0193-z
  14. Johnsen PB, Adams MA. Chemical feeding stimulants for the herbivorous fish, Tilapia zillii. Comp Biochem Physiol A Physiol. 1986;83:109-12. https://doi.org/10.1016/0300-9629(86)90096-4
  15. Harrold C, Pearse JS. The ecological role of echinoderms in kelp forests. In: Jangoux M, Lawrence JM, editors. Echinoderm studies. Boca Raton, FL: CRC Press; 1987. p.137-233.
  16. Kane AS, Salierno JD, Brewer SK. Fish models in behavioral toxicology: automated techniques, updates and perspectives. In: Ostrander GK, editor. Methods in aquatic toxicology. Baton Rouge, FL: CRC Press; 2005. p.559-590.
  17. Kermen F, Franco LM, Wyatt C, Yaksi E. Neural circuits mediating olfactory-driven behavior in fish. Front Neural Circuits. 2013;7:62.
  18. Kuklina I, Kouba A, Kozak P. Real-time monitoring of water quality using fish and crayfish as bio-indicators: a review. Environ Monit Assess.2013;185:5043-53. https://doi.org/10.1007/s10661-012-2924-2
  19. Lang C, Mann KH. Change in sea urchin populations after the destruction of kelp beds. Mar Biol. 1976;36:321-6. https://doi.org/10.1007/BF00389193
  20. Lawrence JM. Sea urchin: biology and ecology. 2nd ed. Amsterdam: Elsevier Science; 2007.
  21. Little EE, Brewer SK. Neurobehavioral toxicity in fish. In: D Schlenk, Benson WH, editors. Target organ toxicity in marine and freshwater teleosts. London: Taylor and Francis; 2001. p.141-76.
  22. Lokkeborg S, Siikavuopio SI, Humborstad OB, Utne-Palm AC, Ferter K. Towards more efficient longline fisheries: fish feeding behaviour, bait characteristics and development of alternative baits. Rev Fish Biol Fisher. 2014;24:985-1003. https://doi.org/10.1007/s11160-014-9360-z
  23. Lowry M, Steffe A, Williams D. Relationships between bait collection, bait type and catch: a comparison of the NSW trailer-boat and gamefish-tournament fisheries. J Fisher Res. 2006;78:266-75. https://doi.org/10.1016/j.fishres.2005.11.014
  24. Mas-Munoz J, Komen H, Schneider O, Visch SW, Schrama JW. Feeding behavior, swimming activity and boldness explain variation in feed intake and growth of Sole (Solea solea) reared in captivity. PLOS ONE. 2011;6:e21393. https://doi.org/10.1371/journal.pone.0021393
  25. Niu B, Li G, Peng F, Wu J, Zhang L, Li Z. Survey of fish behavior analysis by computer vision. J Aquac Res Dev. 2018;9:1-15.
  26. Noldus LPJJ, Spink AJ, Tegelenbosch RAJ. EthoVision: a versatile video tracking system for automation of behavioral experiments. Behav Res Methods Instrum Comput. 2001;33:398-414. https://doi.org/10.3758/BF03195394
  27. Qin L, Zhu BW, Zhou DY, Wu HT, Tan H, Yang JF, et al. Preparation and antioxidant activity of enzymatic hydrolysates from purple sea urchin (Strongylocentrotus nudus) gonad. LWT-Food Sci Technol. 2011;44:1113-8. https://doi.org/10.1016/j.lwt.2010.10.013
  28. Rune V, Geir H, Anders F, Terje J, Svein L, Georg S. Simulating search behaviour of fish towards bait. ICES J Marine Sci. 2004;61:1224-32. https://doi.org/10.1016/j.icesjms.2004.06.001
  29. Smith PA. The relationship between stock and catch and the effect of bait on catch as determined for a UK recreational catch and release fishery. Fish Manage Ecol. 2002;9:261-6. https://doi.org/10.1046/j.1365-2400.2002.00311.x
  30. Siliani S, Melis R, Loi B, Guala G, Baroli M, Sanna S, et al. Influence of seasonal and environmental patterns on the lipid content and fatty acid profiles in gonads of the edible sea urchin Paracentrotus lividus from Sardinia. Mar Environ Res. 2016;113:124-33. https://doi.org/10.1016/j.marenvres.2015.12.001
  31. Suresh AV, Kumaraguru vasagam KP, Nates S, Attractability and palatability of protein ingredients of aquatic and terrestrial animal origin, and their practical value for blue shrimp, Litopenaeus stylirostris fed diets formulated with high levels of poultry byproduct meal. Aquaculture 2011;319:132-40. https://doi.org/10.1016/j.aquaculture.2011.06.039
  32. Umar T, Sitkun D, Asri A. The influence of using bait types to the number and composition of fishing traps catch in south ternate waters. IOP Conf Ser Earth Environ Sci. 2018;175:012231. https://doi.org/10.1088/1755-1315/175/1/012231
  33. Vabo R, Huse G, Ferno A, Jorgensen T, Lokkeborg S, Skaret G. Simulating search behaviourof fish towards bait. ICES J Mar Sci. 2004;61:1224-32. https://doi.org/10.1016/j.icesjms.2004.06.001
  34. Valentine JF, Heck KL. Seagrass herbivory: evidence for the continued grazing of marine grasses. Mar Ecol Prog Ser.1999;176:291-302. https://doi.org/10.3354/meps176291
  35. Woll AK, Boje J, Holst R, Gundersen AC. Catch rates and hook and bait selectivity in longline fishery for Greenland halibut (Reinhardtius hippoglossoides, Walbaum) at East Greenland. Fish Res. 2001;51:237-46. https://doi.org/10.1016/S0165-7836(01)00249-1
  36. Zhao S, Cheng Q, Peng Q, Yu X, Yin X, Liang M, et al. Antioxidant peptides derived from the hydrolyzate of purple sea urchin (Strongylocentrotus nudus) gonad alleviate oxidative stress in Caenorhabditis elegans. J Funct Food. 2018;48:594-604. https://doi.org/10.1016/j.jff.2018.07.060