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Different wavelengths of light influence daily swimming activity in silver catfish (Rhamdia quelen)

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The aim of this study was to investigate the daily rhythms of swimming activity in Rhamdia quelen maintained under different wavelengths of light. Thirty fish were equally divided into ten 100 liters tanks. The water temperature was maintained at 25±0.2ºC. In each tank, an infrared photocell was installed. The tanks were equipped with RGB LED strips placed at the top. Fishes were exposed to different 7 day-periods of 12/12 light/dark hours. In each period, a different light color was used: white (150 lux), red (12 lux), green (180 lux), blue (50 lux), and again white (150 lux). The application of cosinor-based techniques for the analysis of time series showed a daily rhythm of swimming activity in all tanks, in all experimental conditions. Acrophase was diurnal during the first white light schedule, on the second day of red light it was observed at the beginning of the light phase. During the green and blue schedules, acrophase was observed during the dark phase of the experimental photoperiod. In the second white schedule, it shifted in the middle of the light phase. Robustness was variable among the different lighting schedules and days of monitoring. The application of two-way of repeated measure analysis of variance showed a statistical effect of experimental lighting and day of monitoring on all rhythmic parameters. In conclusion, Rhamdia quelen lives in the deep regions of rivers, this could be the reason because the green lighting creates a reasonable environment that does not disturb the biological clock driving the swimming activity in this fish species. This information could be useful for application in aquaculture to improve fish welfare, reduce costs, and increase productivity.

Wu Y, Yan H, Shen X, et al. Effects of different light conditions on growth, muscle nutrients content, and clock gene circadian expression of Takifugu rubripes. Aquac Rep 2022;26:101294. DOI: https://doi.org/10.1016/j.aqrep.2022.101294
Koukkari WL, Sothern RB. Introducing biological rhythms. Springer, New York; 2006.
Foster RF, Hankins MW, Peirson S. Light, photoreceptors, and circadian clocks. In: E. Rosato (Eds) Circadian rhythms. Methods and protocols. pp. 3-28. Humana Press, Totowa, NJ; 2007. DOI: https://doi.org/10.1007/978-1-59745-257-1_1
Shin HS, Lee J, Choi CY. Effects of LED light spectra on oxidative stress and the protective role of melatonin in relation to the daily rhythm of the yellowtail clownfish, Amphiprion clarkii. Comp Biochem Physiol A 2011;160:221-8. DOI: https://doi.org/10.1016/j.cbpa.2011.06.002
Dunlap JC, Loros JJ, DeCoursey PJ. Chronobiology, Biological timekeeping. Sinauer Associates, Sunderland; 2004
Bertolucci C, Sovrano VA, Magnone MC, Foa A. Role of suprachiasmatic nuclei in ircadian and light-entrained behaioral rhythm in lizars. Am J Physiol Regul Integr Comp Physiol 2000; 279:R2121-31 DOI: https://doi.org/10.1152/ajpregu.2000.279.6.R2121
Foa A, Brandstatter R, Bertolucci C. The circadian system of ruin lizards: a seasonally changing neuroenorine loop? Choobiol Int 2006;23:317-27. DOI: https://doi.org/10.1080/07420520500521954
Watanabe N, Itoh K, Fujinami Y, et al. Circadian pacemaker in the suprachiasmatic nuclei of teleost fish reealed by rhythmic period2 expression. Gen Comp Endocrinol 2012;178:400-7. DOI: https://doi.org/10.1016/j.ygcen.2012.06.012
Noche RR, Lu PN, Goldstein-Kral L, et al. Circadian rhythms in the pineal organ persist in zebrafish larvae that lack ventral brain. BMC Neurosci 2011;12:7. DOI: https://doi.org/10.1186/1471-2202-12-7
Zhadanova IV, Reebs SG. Circadian rhythm in fish. Fish Physiol 2006;24:197-238. DOI: https://doi.org/10.1016/S1546-5098(05)24006-2
Vatine G, Vallone D, Gothilf Y, Foulkes NS. It’s time to swim! Zebrafish and the circadian clock. FEBS Lett 2011;585:1485-94. DOI: https://doi.org/10.1016/j.febslet.2011.04.007
Sánchez-Vázquez FJ, López-Olmeda JF, Vera LM, et al. Environmental cycles, melatonin, and circadian control of stress response in fish. Front Endocrinol 2019;10:279. DOI: https://doi.org/10.3389/fendo.2019.00279
Villamizar N, Blanco-Vives B, Migaud H, et al. Effects of light during early larval development of some aquaculture teleosts: a review. Aquaculture 2011;315:86-94. DOI: https://doi.org/10.1016/j.aquaculture.2010.10.036
Baldisserotto B. The emerging silver catfish culture in Latin America. Aquaculture 2003;29:36-40.
Valladão GM, Gallani SU, Pilarski F. South American fish for continental aquaculture. Rev Aquac 2018;10:351-69. DOI: https://doi.org/10.1111/raq.12164
Migaud H, Cowan M, Taylor J, Ferguson HW. The effects of spectral composition and light intensity on melatonin, stress and retinal damage in post-smolt Atlantic salmon, Salmo salar. Aquaculture 2007;270:390-404. DOI: https://doi.org/10.1016/j.aquaculture.2007.04.064
Carbonaro DA, Friend TH, Dellmeier GR. Behavioral and physiological responses of dairy goats to isolation. Physiol Behav 1992;51:297-301. DOI: https://doi.org/10.1016/0031-9384(92)90144-Q
Nelson W, Tong U, Lee J, Halberg F. Methods for cosinor rhythmometry. Chronobiologia 1979;6:305-23.
Lythgoe JN. The ecology of vision. Clarendon Press, Oxford; 1979.
Choi CY, Song JA, Lee TH, Park YS. Effect of green wavelength light on stress and appetite responses of olive flounder (Paralichthys olivaceus) following feed deprivation and re-feeding. Aquac Rep 2021;19:100605. DOI: https://doi.org/10.1016/j.aqrep.2021.100605
Bayarri MJ, Madrid JA, Sánchez-Vázquez FJ. Influence of light intensity, spectrum and orientation on sea bass plasma and ocular melatonin. J Pineal Res 2002;32:34-40. DOI: https://doi.org/10.1034/j.1600-079x.2002.10806.x
Vera LM, Davie A, Taylor JF, Migaud H. Differential light intensity and spectral sensitivities of Atlantic salmon, European sea bass and Atlantic cod pineal glands ex vivo. Gen Comp Endocriol 2010;165:25-33. DOI: https://doi.org/10.1016/j.ygcen.2009.05.021
Villamizar N, Garcia-Alcazar A, Sanchez-Vazquez FJ. Effect of light spectrum and photoperiod on the growth, development and survival of European sea bass (Dicentrarchus labrax) larvae. Aquaculture 2009;292:80-86. DOI: https://doi.org/10.1016/j.aquaculture.2009.03.045
Blanco-Vives B, Villaizar N, Ramos J, et al. Effect of daily thermo- and photo-cycles of different light spectrum on the development of Senegal sole (Solea senegalensis) larvae. Aquaculture 2010;306:137-45. DOI: https://doi.org/10.1016/j.aquaculture.2010.05.034
Downing G, Litak MK. The effect of light intensity and spectrum on the incidence of first feeding by larval haddock. J Fish Biol 2001;59:1566-78. DOI: https://doi.org/10.1006/jfbi.2001.1792
Winemiller KO. Patterns of variation in life history among South American fishes in seasonal environment. Oecologia 1989;81:225-41. DOI: https://doi.org/10.1007/BF00379810
Gomes LC, Colombieski JL, Gomes ARC, Baldiserotto B. Biologia do jundia Rhamdia quelen (Teleostei, Pimelodidae). [Biology of jundia Rhamdia quelen (Teleostei, Pimelodidae)] Ciencia Rural 2000;30:179-85. DOI: https://doi.org/10.1590/S0103-84782000000100029
Scaglione MC, Cerutti RD, Arfuso F, Piccione G. Light and dark rations and the photic entrainment of circadian locomotor activity patterns in the Southern American Silver Catfish (Rhamdia quelen, Quoy &Gaimard, 1824). Biol Rhythm Res 2018;49:129-40. DOI: https://doi.org/10.1080/09291016.2017.1336881
Giannetto C, Casella S, Caola G, Piccone G. Photic and non photic entrainment on the daily rhythm of locomotor activity in goats. Anim Sci J 2010;81:122-28. DOI: https://doi.org/10.1111/j.1740-0929.2009.00707.x
Iigo M, Furukawa K, Tabata M, Aida K. Circadian variations of melatonin binding sites in the goldfish brain. Neurosci Lett 2003;347:49-52. DOI: https://doi.org/10.1016/S0304-3940(03)00636-0
Park MS, Shin HS, Kim NN, et al. Effects of LED spectral sensitivity on circadian rhythm-related genes in the yellowtail clownfish, Amphiprion clarkii. Anim Cell Syst 2013;2:99-105. DOI: https://doi.org/10.1080/19768354.2013.779935
van der Merwe I, Bennet NC, Haim A, Oosthuizen K. Effects of the colour of photophase light of locomotor activity in a nocturnal and a diurnal South Africa rodent. Biol Lett 2019;15:1-6. DOI: https://doi.org/10.1098/rsbl.2019.0597
Bonmati-Carrion MA, Bano-Otalora B, Madrid JA, Rol MA. Light color importance for ircadian entrainment in a diurnal (Octodon degus) and a nocturnal (Rattus norvegicus) rodent. Sci Rep 2017;7:8845. DOI: https://doi.org/10.1038/s41598-017-08691-7
Lanteri G, Giardina A, Arfuso F, et al. Photic entrainment of daily rhythm pattern of locomotor activity in sea bass (Dicentrarcus labrax). Biol Rhythm Res 2016;47:69-76. DOI: https://doi.org/10.1080/09291016.2015.1084154

How to Cite

Giannetto, C., Arfuso, F., Scaglione , M. C., Piccione, G., Faggio, C., Arrigo, F., & Cerutti, R. D. (2025). Different wavelengths of light influence daily swimming activity in silver catfish (<i>Rhamdia quelen</i>). Journal of Biological Research - Bollettino Della Società Italiana Di Biologia Sperimentale. https://doi.org/10.4081/jbr.2025.12475

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