Brown Banana Leaf (Musa x paradisiaca) Improve Betta splendens Hatching, Larvae, Survival and Growth Performance While Affecting its Sex Ratio

Authors

Keywords:

Larvae culture, Ornamental fish, Phytochemicals

Abstract

The effectiveness of brown banana leaf (BBL) Musa x paradisiaca as a culture media for rearing Betta splendens larvae was investigated. Larvae (n=630, 3 days old, 6 replicates) were reared in 7 rearing medium; C1 (no leaf, control), C2 (0.7 g brown catappa leaf, positive control), T1 (0.7 g; Treatment 1), T2 (0.8 g; Treatment 2), T3 (0.9 g, Treatment 3), T4 (1.0 g, Treatment 4) and T5 (1.1 g, Treatment 5) of BBL per litre of rearing water respectively. Throughout the 80 days trial period, larvae were first fed microworms twice daily for two weeks, then Artemia for another two weeks, followed by ad libitum feeding of commercial feed twice daily. Water quality was monitored every two days, and water was changed every two weeks. The hatching rate, survival, growth parameters and sex ratio were determined after 80 days.  There were significant differences (P<0.05) in all the parameters observed.  The highest hatching and survival rates were found in treatment C2 (95.86%; 95.56%) and T5 (95.63%; 95.56%). For treatment T1, T2, T3 and T4, the hatching (HR) and survival rate (SR) was 85.75±7.31% (HR), 68.89±13.11% (SR); 75.54±2.04% (HR),76.67±15.64% (SR);  89.76±0.587% (HR), 74.44±22.08% (SR) and 92.63±2.23% (HR), 61.11±6.56% (SR) respectively. The lowest percentage of hatching rate was shown by C1 at 68.08±1.089% while the lowest survival rate was shown by T4. The highest specific growth rate (SGR) was T3 (6.00±0.34% day-1) (weight) and T5 (3.45±0.10% day-1) (length). The SGR for C2, TI, T2 and T4 was recorded at 5.837±0.34, 5.857±0.5, 5.81±0.429 and 5.612±0.243 % day-1 respectively. The sex ratios were skewed in 2 treatments; T1 (12 male: 19 female) and T5 (19 male: 9 female) with the rest showing no significant difference to the 50:50 (M:F) ratio. Hatching rate, SGR and sex ratio was not recorded for C1 as all larvae reached 100% mortalities after two weeks of the rearing trials.  Based on the result, it is safe to conclude that BBL is a good and safe alternative/replacement to catappa leaf for usage in the aquaculture industry.

References

Abbas, A.K., Lichtman, A.H. & Pillai, S. (2019). Basic immunology E-book: functions and disorders of the immune system. Sixth Edition. Philadelphia: Elsevier.

Abdellatief, S.A., Abdel Rahman, A.N. & Abdallah, F.D. (2018). Evaluation of immunostimulant activity of Spirulina platensis (Arthrospira platensis) and Sage (Salvia officinalis) in Nile tilapia (Oreochromis niloticus). Zagazig Veterinary Journal, 46, 25-36. DOI: https://doi.org/10.21608/zvjz.2018.7621

Ahmadifar, E., Pourmohammadi Fallah, H., Yousefi, M., Dawood, M.A.O., Hoseinifar, S.H., Adineh, H., Yilmaz, S., Paolucci, M. & Doan, H.V. (2021). The gene regulatory roles of herbal extracts on the growth, immune system, and reproduction of fish. Animals, 11(8), 2167. DOI: https://doi.org/10.3390/ani11082167

Annegowda, H.V., Nee, C.W., Mordi, M.N., Ramanathan, S., & Mansor, S.M. (2010). Hydrolysed extracts of Terminalia catappa L. leaf. Asian Journal of Plant Sciences, 9(8), 479–485. DOI: https://doi.org/10.3923/ajps.2010.479.485

Ashraf, M. & Bengtson, D.A. (2007). Effect of tannic acid on feed intake, survival and growth of striped bass (Morone saxatilis) larvae. International Journal of Agriculture and Biology, 9, 751-754. DOI: https://doi.org/10.30574/wjarr.2023.17.1.1157

Aswadi, N.I.A. (2023). Elucidating the potential of banana leaf (Musa x paradisiaca) in siamese fighting fish (Betta splendens) production. (Master Thesis), Universiti Malaysia Terengganu, Malaysia.

Aziz, M.A., Mostary, M.M., Sume, I.J., Uddin, M.H., Khan, M.G.Q., Alam, M.S. & Islam, M. S. (2022). The efficacy of using pine (Pinus massoniana) pollen as an alternative to synthetic steroids in producing monosex male Nile tilapia (Oreochromis niloticus, L.). Aquaculture, Fish and Fisheries, 2(5), 375-383. DOI: https://doi.org/10.1002/aff2.59

Baumgartner, G., Nakatani, K., Gomes, L.C., Bialetzki, A., Sanches, P.V. & Makrakis, M.C. (2008). Fish larvae from the upper Paraná River: do abiotic factors affect larval density? Neotropical Ichthyology, 6, 551-558. DOI: https://doi.org/10.1590/S1679-62252008000400002

Bell, G.R., Hoskins, G.E. & Bagshaw, J.W. (1969). On the structure and enzymatic degradation of the external membrane of the salmon egg. Canadian Journal of Zoology, 47, 146-148. DOI: https://doi.org/10.1139/z69-028

BERNAMA. (2024). DOF committed to support high-potential ornamental fish industry. https://bernama.com/en/news.php?id=2310154. Downloaded on 13 October 2025.

Berrino, F., Bellati, C., Secreto, G., Camerini, E., Pala, V., Panico, S., Allegro, G. & Kaaks, R. (2001). Reducing bioavailable sex hormones through a comprehensive change in diet: the diet and androgens (DIANA) randomized trial. Cancer Epidemiology Biomarkers & Prevention, 10(1), 25-33. https://aacrjournals.org/cebp/article/10/1/25/164016/Reducing-Bioavailable-Sex-Hormones-through-a

Calberto, G., Staver, G. C. & Siles, P. (2015). An assessment of global banana production and suitability under climate change scenarios. In Elbehri, A. (ed.) Climate change and food systems: Global assessments and implications for food security and trade. Food Agriculture Organization of the United Nations (FAO). pp. 266-291.

Carnevali, O., Cardinali, M., Maradonna, F., Parisi, M., Olivotto, I., Polzonetti-Magni, A.M., Mosconi, G. & Funkenstein, B. (2005). Hormonal regulation of hepatic IGF-I and IGF-II gene expression in the marine teleost Sparus aurata. Molecular Reproductive and Development: Incorporating Gamete Research, 71(1), 12-18. DOI: https://doi.org/10.1002/mrd.20122

Cek, S., Turan, F. & Atik, E. (2007). The effects of Gokshura, Tribulus terrestris on sex reversal of guppy, Poecilia reticulata. Pakistan Journal of Biological Sciences, 10, 718-725. DOI: https://doi.org/10.3923/pjbs.2007.718.725

Chansue, N. & Assawawongkasem, N. (2011). The in vitro antibacterial activity and ornamental fish toxicity of the water extract of Indian almond leaves (Terminalia catappa Linn.). KKU Veterinary Journal, 18(1), 36-45. http://www.allnaturalpetcare.com/Natural_Aquariums/Indian_Almond_Leaves-Guppies_Bettas_Goldfish.pdf

Chen, X., Hu, Y., Shan, L., Yu, X., Hao, K. & Wang, G.X. (2017). Magnolol and honokiol from Magnolia officinalis enhanced antiviral immune responses against crass carp reovirus in Ctenopharyngodon idella kidney cells. Fish & Shellfish Immunology, 63, 245-254. DOI: https://doi.org/10.1016/j.fsi.2017.02.020

Cheshenko, K., Pakdel, F., Segner, H., Kah, O. & Eggen, R. I. L. (2008). Interference of endocrine disrupting chemicals with aromatase CYP19 expression or activity, and consequences for reproduction of teleost fish. General and Comparative Endocrinology, 155, 31-62. DOI: https://doi.org/10.1016/j.ygcen.2007.03.005

Chitmanat, C., Tongdonmuan, K., Khanom, P., Pachontis, P. & Nunsong, W. (2003). Antiparasitic, antibacterial, and antifungal activities derived from a Terminalia catappa solution against some tilapia (Oreochromis niloticus)

pathogens. In Franz, C., Mathe, A., Craker, L.E. and Gardner, Z.E. (eds.) Acta Horticulturae. III WOCMAP Congress on Medicinal and Aromatic Plants—Volume 4: Targeted Screening of Medicinal and Aromatic Plants, Economics & Law. Chiang Mai, Thailand. pp. 179-182. DOI: https://doi.org/10.17660/ActaHortic.2005.678.25

Citarasu, T. (2010). Herbal biomedicines: A new opportunity for aquaculture industry. Aquaculture International, 18, 403-414. DOI: https://doi.org/10.1007/s10499-009-9253-7

Cogliati, K.M., Corkum, L.D. & Doucet, S.M. (2010). Bluegill coloration as a sexual ornament: evidence from ontogeny, sexual dichromatism, and condition dependence. Ethology, 116, 416-428. DOI: https://doi.org/10.1111/j.1439-0310.2010.01755.x

D’Arrigo, G., Gianquinto, E., Rossetti, G., Cruciani, G., Lorenzetti, S. & Spyrakis, F. (2021). Binding of androgen-and estrogen-like flavonoids to their cognate (non) nuclear receptors: a comparison by computational prediction. Molecules, 26(6), 1613. DOI: https://doi.org/10.3390/molecules26061613

Dabrowski, K., Gustavo, R. & Mary, A. G. A. (2005). Use of phytochemicals as an environmentally friendly method to sex reverse Nile tilapia. In: Burright, J. Flemming, C. and Egna, H. (eds.) Twenty-Second Annual Technical Report. Oregon State University, Aquaculture CRSP. pp. 287-303.

Doctolero, J.S., Estrella, E.S. & Vera Cruz, E.M. (2021). Influence of water immersion using guava (Psidium guajava), lemon-grass (Cymbopogon ciratus) and horse radish (Moringa oleifera) aqueous leaves extract on the nursing of Nile tilapia (Oreochromis niloticus). International Journal of Zoology and Animal Biology, 4(1), 000279. DOI: https://doi.org/10.23880/izab-16000279

Dongmeza, E., Steinbronn, S., Francis, G., Focken, U. & Becker, K. (2009). Investigations on the nutrient and antinutrient content of typical plants used as fish feed in small scale aquaculture in the mountainous regions of Northern Vietnam. Animal Feed Science and Technology, 149(1-2), 162-178. DOI: https://doi.org/10.1016/j.anifeedsci.2008.04.012

dos Anjos, H.D.B., Amorim, R.D.S., Siqueira, J.A. & dos Anjos, C.R. (2009). Ornamental fish export of the state of Amazonas, Amazon basin, Brazil. Boletim do Instituto de Pesca, 35(2), 259-274. http://www.pesca.sp.gov.br/sumario35_2.php

dos Santos, J. A., Soares, C. M. & Bialetzki, A. (2020). Effects of pH on the incubation and early development of fish species with different reproductive strategies. Aquatic Toxicology, 219, 105382. DOI: https://doi.org/10.1016/j.aquatox.2019.105382

Evers, H. G., Pinnegar, J. K. & Taylor, M.I. (2019). Where are they all from? Sources and sustainability in the ornamental freshwater fish trade. Journal of Fish Biology, 94(6), 909-916. DOI: https://doi.org/10.1111/jfb.13930

Gabriel, N.N., Qiang, J., Ma, X.Y., He, J., Xu, P. & Omoregie, E. (2017). Sex-reversal effect of dietary Aloe vera (Liliaceae) on genetically improved farmed Nile tilapia fry. North American Journal of Aquaculture, 79(1), 100-105. DOI: https://doi.org/10.1080/15222055.2016.1236046

Gharaei, A., Jorjani, H.E., Harijani, J.M. & Miandare, H.K. (2020). Effects of Tribullus terrestris extract on masculinization, growth indices, sex deteminationreversal and steroid hormones level in Zebra fish (Danio rerio). International Aquatic Research, 12(1), 22-29. DOI: https://doi.org/10.22034/IAR(20).2020.670992

Giri, S.S., Jun, J.W., Sukumaran, V. & Park, S.C. (2016). Dietary administration of banana (Musa acuminata) peel flour affects the growth, antioxidant status, cytokine responses, and disease susceptibility of rohu, Labeo rohita. Journal of Immunology Research, 2016, 4086591. DOI: https://doi.org/10.1155/2016/4086591

Guo, H., Lin, W., Hou, J., Wang, L., Zhang, D., Wu, X., Li, L. & Li, D. (2018). The protective roles of dietary selenium yeast and tea polyphenols on growth performance and ammonia tolerance of juvenille Wuchang bream (Megalobrama amblycephala). Frontiers in Phyciology, 9, 1371. DOI: https://doi.org/10.3389/fphys.2018.01371

Hagenmaier, H.E. (1974). The hatching process in fish embryos IV. The enzymological properties of a highly purified enzyme (chorionase from the hatching fluid of the rainbow trout. Salmo gairdneri Rich.). Comparative Biochemistry and Physiology, 49, 313-324. DOI: https://doi.org/10.1016/0305-0491(74)90166-7

Herath, S. & Atapaththu, K. (2012). Effects of different live feeds on growth performance of fighter fish (Betta Splendens) larvae. The 2nd International Symposium, 25-27 May 2012. South Eastern University of Sri Lanka. pp. 129-131. http://ir.lib.seu.ac.lk/handle/123456789/2844

Immanuel, G., Uma, R., Iyapparaj, P., Citarasu, T., Punitha Peter, S., Michael Babu, M. & Palavesam, A. (2009). Dietary medicinal plant extracts improve growth, immune activity and survival of tilapia Oreochromis mossambicus. Journal of Fish Biology, 74(7), 1462-1475. DOI: 10.1111/j.1095-8649.2009.02212.x

Islam, S.I., Mou, M.J., Sanjida, S. & Mahfuj, S. (2021). An in-silico approach fro identifying phytochemical inhibitors against nervous necrosis virus (NNV) in asian sea bass by targeting capsid protein. Genetics of Aquatic Organism, 6(2), GA487. DOI: 10.4194/GA487

Jezierska, B., Ługowska, K. & Witeska, M. (2009). The effects of heavy metals on embryonic development of fish (a review). Fish Physiology and Biochemistry, 35(4), 625-640. DOI: https://doi.org/10.1007/s10695-008-9284-4

Kadak, A.E., Bilen, S., Ozdemir, R.C. & Sonmez, A.Y. (2019). Effect of ginseng root (Araliaceae sp.) extracts on sperm quality parameters and reproductive performance in rainbow trout (Oncorhynchus mykiss). Israeli Journal of Aquaculture-Bamidgeh, 71, 20992. DOI: http://dx.doi.org/10.46989/001c.20992

Kajimura, M., Takimoto, K. & Takimoto, A. (2023). Acute toxicity of ammonia and nitrite to Siamese fighting fish (Betta splendens). BMC Zoology. 8(25). DOI: https://doi.org/10.1186/s40850-023-00188-3

Kamboh, A.A. & Zhu, W.Y. (2013). Effect of increasing levels of bioflavonoids in broiler feed on plasma anti-oxidative potential, lipid metabolites, and fatty acid composition of meat. Poultry Science, 92(2), 454-461. DOI: https://doi.org/10.3382/ps.2012-02584

Kareem, O.K., Ajani, E.K., Akintunde, M.A., Olanrewaju, A.N. & Oduntan, O.B. (2017). Effect of different fertilization and egg de-adhesion methods on hatching and survival of Clarias gariepinus (Burchell 1822) fry. Journal of Fisheries Sciences.com, 11(1), 21-27. DOI: http://dx.doi.org/10.21767/1307-234X.1000103

Katare, M.B., Basavaraja, N., Joshi, H.D. & Archana, C. (2015). Effect of letrozole on masculinization of Siamese fighting fish (Betta splendens). Journal of Applied and Natural Science, 7(1), 425-433. DOI: https://doi.org/10.31018/jans.v7i1.627

Kema, G.H., Drenth, A., Dita, M., Jansen, K., Vellema, S. & Stoorvogel., J.J. (2021). Fusarium wilt of banana, a recurring threat to global banana production. Frontiers in Plant Science, 11, 628888. DOI: https://doi.org/10.3389/fpls.2020.628888

Khumpirapang, N., Sassa-Deepaeng, T., Suknuntha, K., Anuchapreeda, S. & Okonogi, S. (2021). Masculinizing effects of chrysin-loaded poloxamer micelles on Siamese fighting fish. Veterinary Sciences, 8(12), 305. DOI: https://doi.org/10.3390/vetsci8120305

Kumar, S., Raman, R.P., Pandey, P.K., Mohanty, S., Kumar, A. & Kumar, K. (2013). Effect of orally administered azadirachtin on non-specific immune parameters of goldfish Carassius auratus (Linn. 1758) and resistance against Aeromonas hydrophila. Fish Shellfish Immunology, 34, 564-573. DOI: https://doi.org/10.1016/j.fsi.2012.11.038

Laerd. (2022). Statistics Laerd. Available at: htttps://statistics.laerd.com.

Lichak, M. R., Barber, J. R., Kwon, Y. M., Francis, K. X. & Bendesky, A. (2022). Care and use of Siamese fighting fish (Betta splendens) for research. Comparative Medicine, 72(3), 169-180. DOI: https://doi.org/10.30802/AALAS-CM-22-000051

Makled, S.O., Hamdan, A.M. & El-Sayed, A.F.M. (2020). Growth promotion and immune stimulation in nile tilapia, Oreochromis niloticus, fingerlings following dietary administration of a novel marine probiotic, Psychrobacter maritimus S. Probiotics and Antimicrobial Proteins, 12(2), 365-374. DOI: https://doi.org/10.1007/s12602-019-09575-0

Mallik, J., Al, F.A. & Kumar, B.R. (2018). A Comprehensive review on pharmacological activity of Terminalia catappa (Combretaceae) - An update. Asian Journal of Pharmaceutical Research and Development, 1(2), 65–70.

Mandal, S.C., Sahu, N.P., Kohli, M.P.S., Das, P., Gupta, S.K. & Munilkumar, S. (2010). Replacement of live feed by formulated feed: effect on the growth and spawning performance of Siamese fighting fish (Betta splendens, Regan, 1910). Aquaculture Research, 41(11), 1707-1716. DOI: https://doi.org/10.1111/j.1365-2109.2010.02564.x

Marimuthu, K., Palaniandya, H. & Muchlisin, Z.A. (2019). Effect of different water pH on hatching and survival rates of African catfish Clarias gariepinus (Pisces: Clariidae). Aceh Journal of Animal Science, 4(2), 80-88. DOI: https://doi.org/10.13170/ajas.4.2.13574

Matthews, J., Celius, T., Halgren, R. & Zacharewski, T. (2000). Differential estrogen receptor binding of estrogenic substances: a species comparison. The Journal of Steroid Biochemistry and Molecular Biology, 74(4), 223-234. DOI: https://doi.org/10.1016/S0960-0760(00)00126-6

Mehrabi, Z., Firouzbakhsh, F., Rahimi-Mianji, G. & Paknejad, H. (2020). Immunity and growth improvement of rainbow trout (Oncorhynchus mykiss) fed dietary nettle (Urtica dioica) against experimental challenge with Saprolegnia parasitica. Fish & Shellfish Immunology, 104, 74-82. DOI: https://doi.org/10.1016/j.fsi.2020.05.050

Midhun, S.J., Arun, D., Edatt, L., Sruthi, M., Thushara, V., Oommen, O.V., Kumar, V.S. & Divya, L. (2016). Modulation of digestive enzymes, GH, IGF-1 and IGF-2 genes in the teleost, Tilapia (Oreochromis mossambicus) by dietary curcumin. Aquaculture International, 24, 1277-1286. DOI: https://doi.org/10.1007/s10499-016-9984-1

Mukherjee, D., Ghosal, I. & Chakraborty, S.B. (2015). Production of monosex Nile tilapia, Oreochromis niloticus using seed of Mucuna pruriens. IOSR Journal of Pharmacy and Biological Sciences, 10, 55-59. DOI: 10.9790/3008-10145559

Murray, C.A., Markham, O.I., Wood, A.L. & Dimaggio, M. A. (2024). Developing efficient feeding and weaning protocols for Betta splendens informed by larval digestive physiology. Aquaculture, 587, 740884. DOI: https://doi.org/10.1016/j.aquaculture.2024.740884

Nagahama, Y. (2002). Endocrine regulation of gametogenesis in fish. International Journal of Developmental Biology, 38(2), 217-229. DOI: https://pubmed.ncbi.nlm.nih.gov/7981031/

Nakamura, M., Kobayashi, T., Chang, X.T. & Nagahama, Y. (1998). Gonadal sex differentiation in teleost fish. Journal of Experimental Zoology, 281(5), 362-372. DOI: https://doi.org/10.1002/(SICI)1097-010X(19980801)281:5%3C362::AID-JEZ3%3E3.0.CO;2-M

Neelavathi, P., Venkatalakshmi, P. & Brindha, P. (2013). Antibacterial activities of aqueous and ethanolic extracts of Terminalia catappa leaves and bark against some pathogenic bacteria. International Journal of Pharmacy and Pharmaceutical Sciences, 5(1), 114–120.

Ng, Y., Hanson, S., Malison, J.A., Wentworth, B. & Barry, T.P. (2006). Genistein and other isoflavones found in soybeans inhibit estrogen metabolism in salmonid fish. Aquaculture, 254, 658-665. DOI: https://doi.org/10.1016/j.aquaculture.2005.10.039

Nian, C.T., Tumbokon, B.L.M. & Serrano, A.E. (2017). Pinus tabulaeformis pollen as replacement for 17-alpha-methyltestosterone in the diet of Oreochromis niloticus larvae for sex reversal and growth. Israeli Journal of Aquaculture-Bamidgeh, 69, 1-8. DOI: http://dx.doi.org/10.46989/001c.21042

Norazmi-Lokman, N. H., Baderi, A. A., Zabidi, Z. M. & Diana, A.W. (2020). Effects of different feeding frequency on Siamese fighting fish (Betta splenden) and Guppy (Poecilia reticulata) juveniles: Data on growth performance and survival rate. Data in Brief, 32, 106046. DOI: https://doi.org/10.1016/j.dib.2020.106046

Norazmi-Lokman, N.H. & Aswadi, N.I.A. (2023). Raw data on the phytochemical content of banana leaf (Musa x paradisiaca) and Betta splendens rearing water containing Brown Banana leaf (Musa x paradisica) along with main water quality data of the rearing water, Mendeley Data, V4. DOI: https://doi.org/10.17632/9rh4tdwy57.4

Nugroho, R.A., Manurung, H., Saraswati, D., Ladyescha, D. & Nur, F.M. (2016). The effects of Terminalia catappa L. leaves extract on the water quality properties, survival and blood profile of ornamental fish (Betta sp.) cultured. Biosaintifika: Journal of Biology & Biology Education, 8(2), 240-247. DOI: https://doi.org/10.15294/biosaintifika.v8i2.6519

Olaniyi, C.O., Adebowale, T.T. & Mustapha, R.O. (2016). Effect of mulberry leaf meal on growth and reproductive performance of African catfish. CIBTech Journal of Zoology, 5(2), 20-24.

Omeje, V.O. (2016). Effect of Pawpaw (Carica papaya) seed meal on the reproductive, endocrine and immune system of Mozambique tilapia (Oreochromis mossambicus) (PhD thesis), Stellenbosch University, South Africa.

Panase, P., Kamee, B., Moungmor, S., Tipdacho, P., Matidtor, J. & Sutthi, N. (2018). Effects of Euphorbia hirta plant leaf extract on growth performance, hematological and organosomatic indices of hybrid catfish, Clarias macrocephalus× C. gariepinus. Fisheries science, 84(6), 1025-1036. DOI: https://doi.org/10.1007/s12562-018-1234-1

Pattiasina, B., Pattinasarany, M., Manuputty, M. & Kokmesa, E. (2021). Masculinization of beta fish larvae Betta splendens through the different treatment immersion of honey solution and larval age. IOP Conference Series: Earth and Environmental Science, 797, 012016. DOI: 10.1088/1755-1315/797/1/012016

Peterson, R.H. & Martin-Robichaud, D.J. (1983). Embryo movements of Atlantic salmon (Salmo salar) as influenced by pH, temperature, and state of development. Canadian Journal of Fisheries and Aquatic Sciences, 40(6), 777-782. DOI: https://doi.org/10.1139/f83-100

Pilsakova, L., Riecanský, I. & Jagla, F. (2010). The physiological actions of isoflavone phytoestrogens. Physiological Research, 59(5), 651. DOI: https://doi.org/10.33549/physiolres.931902

Prusty, A.K., Sahu, N., Pal, A., Reddy, A. & Kumar, S. (2007). Effect of dietary tannin on growth and haemato-immunological parameters of Labeo rohita (Hamilton) fingerlings. Animal Feed Science and Technology, 136(1-2), 96-108. DOI: https://doi.org/10.1016/j.anifeedsci.2006.08.023

Rahmatulloh, M.R., Elfitasari, T. & Windarto, S. (2023). Marketing Analysis of Betta Fish (Betta sp.) Cultivation in Semarang City. IOP Conference Series: Earth and Environmental Science, 1224(1), 012008. DOI: https://doi.org/10.1088/1755-1315/1224/1/012008

Rajapakshe, W. & Srikrishnan, R. (2020). Evaluation of growth performance and breeding habits of fighting fish (Betta splendens) under 3 diets and shelters. Fisheries Science, 3(2), 50-65. doi: 10.18331/SFS2017.3.2.6

Ramos, F.M., Abe, H.A., Couto, M.V.S.D., Paixão, P.E.G., Martins, M.L., Carneiro, P.C.F., Maria, A.N. & Fujimoto, R.Y. (2020). Terminalia catappa improves growth performance and survival of the Amazon leaf fish (Monocirrhus polyacanthus) larvae submitted to handling stress. Aquaculture Research, 51(11), 4805-4808. DOI:https://doi.org/10.1111/are.14783

Rearick, D.C., Fleischhacker, N.T., Kelly, M.M., Arnold, W.A., Novak, P.J. & Schoenfuss, H.L. (2014). Phytoestrogens in the environment, I: occurrence and exposure effects on fathead minnows. Environmental Toxicology and Chemistry, 33(3), 553-559. DOI: https://doi.org/10.1002/etc.2461

Reverter, M., Bontemps, N., Lecchini, D., Banaigs, B. & Sasal, P. (2014). Use of plant extracts in fish aquaculture as an alternative to chemotherapy: current status and future perspectives. Aquaculture, 433, 50-61. DOI: https://doi.org/10.1016/j.aquaculture.2014.05.048

Ribeiro, C., Urbatzka, R., Castro, L.F.C., Carrola, J., Fontainhas-Fernandes, A., Monteiro, R. A., Rocha, M. & Rocha, M.J. (2012). In vitro exposure of Nile tilapia (Oreochromis niloticus) testis to estrogenic endocrine disrupting chemicals: mRNA expression of genes encoding steroidogenic enzymes. Toxicology Mechanisms and Methods, 22(1), 47-53. DOI: https://doi.org/10.3109/15376516.2011.593053

Rosales, C. & Uribe-Querol, E. (2017). Phagocytosis: A fundamental process in immunity. BioMed Research International, 2017, 9042851. DOI: https://doi.org/10.1155/2017/9042851

Rosidah, W.L. & Pratiwy, F.M. (2022). A mini-review: Potential utilization of Morinda citrifolia for health and growth of fish. International Journal of Fisheries and Aquatic Studies, 10(2), 133–137.

Safari, R., Hoseinifar, S.H., Imanpour, M.R., Mazandarani, M., Sanchouli, H. & Paolucci, M. (2020). Effects of dietary polyphenols onmucosal and humoral immune responses, antioxidant defense and growth gene expression in beluga sturgeon (Huso huso). Aquaculture, 528, 735494. DOI: https://doi.org/10.1016/j.aquaculture.2020.735494

Sakai, M. (1999). Current research status of fish immunostimulants. Aquaculture, 172(1-2), 63-92. DOI: https://doi.org/10.1016/S0044-8486(98)00436-0

Salinas, I., Zhang, Y.A. & Sunyer, J.O. (2011). Mucosal immunoglobulins and B cells of teleost fish. Developmental & Comparative Immunology, 35(12), 1346-1365. DOI: https://doi.org/10.1016/j.dci.2011.11.009

Sapkale, P., Singh, R. & Desai, A. (2011). Optimal water temperature and pH for development of eggs and growth of spawn of common carp (Cyprinus carpio). Journal of Applied Animal Research, 39(4), 339-345. DOI: https://doi.org/10.1080/09712119.2011.620269

Secombes, C.J. & Wang, T. (2012). The innate and adaptive immune system of fish. In Infectious disease in aquaculture. England: Woodhead. pp. 3-68.

Serradell, A., Torrecillas, S., Makol, A., Valdenegro, V., Fernández-Montero, A., Acosta, F., Izquierdo, M. & Montero, D. (2020). Prebiotics and phytogenics functional additives in low fish meal and fish oil based diets for European sea bass (Dicentrarchus labrax): Effects on stress and immune responses. Fish & Shellfish Immunology, 100, 219-229. DOI: https://doi.org/10.1016/j.fsi.2020.03.016

Shirmohammadli, Y., Efhamisisi, D. & Pizzi, A. (2018). Tannins as a sustainable raw material for green chemistry: A review. Industrial Crops and Products, 126, 316-332. DOI: https://doi.org/10.1016/j.indcrop.2018.10.034

Silva-Jara, J., Angulo, C., Macias, M.E., Velazquez, C., Guluarte, C. & Reyes-Becerril, M. (2020). First screening report of immune andprotective effect of non-toxic Jatropha vernicosa stem bark against Vibrio parahaemolyticus in Longfin yellowtail Seriola rivoliana leukocytes. Fish & Shellfish Immunology, 101, 106-114. DOI: https://doi.org/10.1016/j.fsi.2020.03.048

Sirotkin, A.V. & Harrath, A.H. (2014). Phytoestrogens and their effects. European Journal of Pharmacology, 741, 230-236. DOI: https://doi.org/10.1016/j.ejphar.2014.07.057

Sopiah, S., Rosidah, R., Lili, W., Iskandar, I. & Suryadi, I.B. (2018). The effectivity of pandanus leaf extract for the treatment of sangkuriang catfish juvenile Clarias gariepinus infected by Aeromonas hydrophila. Jurnal Akuakultur Indonesia, 17(2), 120-129. DOI: https://doi.org/10.19027/jai.17.2.120-129

Sotoudeh, A. & Yeganeh, S. (2017). Effects of supplementary fennel (Foeniculum vulgare) essential oil in diet on growth and reproductive performance of the ornamental fish, Convict cichlid (Cichlasoma nigrofasciatum). Aquaculture Research, 48(8), 4284-4291. DOI: https://doi.org/10.1111/are.13249

Sung, Y.Y. & Abol-Munafi, A. B. (2019). Terminalia catappa leaf extract is an effective rearing medium for larviculture of gouramis. Journal of Applied Aquaculture, 1-11. DOI: https://doi.org/10.1080/10454438.2019.1614509

Syarifuddin, Y.N., Sri, A., Yenny, R. & Rahem, F. A. (2019). Masculinization of tilapia (Oreochromis niloticus) by immersion method using methanol extract of pasak bumi roots (Eurycoma longifolia jack). Russian Journal of Agricultural and Socio-Economic Sciences, 93(9), 79-87. DOI: http://dx.doi.org/10.18551/rjoas.2019-09.08

Tadayon, M., Shojaee, M., Afshari, P., Moghimipour, E. & Haghighizadeh, M.H. (2018). The effect of hydro-alcohol extract of Tribulus terrestris on sexual satisfaction in postmenopause women: A double-blind randomized placebo-controlled trial. Journal of Family Medicine and Primary Care, 7(5), 888-892. DOI: https://doi.org/10.4103%2Fjfmpc.jfmpc_355_17

Turan, F. & Cek, S. (2007). Masculinization of African catfish (Clarias gariepinus) treated with gokshura (Tribulus terrestris). Israeli Journal of Aquaculture Bamidgeh, 59, 224-229. DOI: http://dx.doi.org/10.46989/001c.20528

Uguz, C., Iscan, M. & Toganand, I. (2003). Developmental genetics and physiology of sex differentiation in vertebrates. Environmental Toxicology and Pharmacology, 14, 9-16. DOI: https://doi.org/10.1016/S1382-6689(03)00005-X

Uribe, C., Folch, H., Enríquez, R. & Moran, G.V.J.M. (2011). Innate and adaptive immunity in teleost fish: a review. Veterinarni medicina, 56(10), 486-503. DOI: 10.17221/3294-VETMED.

Watson, C.A., DiMaggio, M., Hill, J.E., Tuckett, Q.M. & Yanong,R.P. (2019). Evolution, culture, and care for Betta splendens. EDIS, FA212, 1–5. DOI: https://doi.org/10.32473/edis-fa212-2019.

Wokeh, O.K. & Orose, E. (2021). Use of dietary phytochemicals as control for excessive breeding in Nile tilapia (Oreochromis niloticus): A review. GSC Biological and Pharmaceutical Sciences, 17(2), 152-159. DOI: https://doi.org/10.30574/gscbps.2021.17.2.0336

Yao, J., Chen, P., Apraku, A., Zhang, G., Huang, Z. & Hua, X. (2019). Hydrolysable Tannin Supplementation Alters Digestibility and Utilization of Dietary Protein, Lipid, and Carbohydrate in Grass Carp (Ctenopharyngodon idellus). Frontiers in Nutrition, 6(183). DOI: https://doi.org/10.3389/fnut.2019.00183

Yeganeh, S., Sotoudeh, A. & Movaffagh, A.N. (2017). Effects of Tribulus terrestris extract on growth and reproductive performance of male convict cichlid (Cichlasoma nigrofasciatum). Turkish Journal of Fisheries and Aquatic Sciences, 17(5), 1003-1007. DOI: 10.4194/1303-2712-v17_5_15

Younes, M. & Honma, N. (2011). Estrogen receptor β. Archives of pathology & laboratory medicine, 135(1), 63-66. DOI: https://doi.org/10.5858/2010-0448-RAR.1

Zou, C., Su, N., Wu, J., Xu, M., Sun, Z., Liu, Q., Chen, L., Zhou, Y., Wang, A. & Ye, C. (2019). Dietary Radix bupleuri extracts improves hepatic lipid accumulation and immune response of hybrid grouper (Epinephelus lanceolatus♂×Epinephelus fuscoguttatus♀). Fish & Shellfish Immunology, 88, 496-507. DOI: https://doi.org/10.1016/j.fsi.2019.02.052

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2025-12-29

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ASRA-ASWADI, N. I. ., KOH, I. C. C. ., ABDUH, M. Y. ., AZRUL-LOKMAN, M. ., & NORAZMI-LOKMAN, N. H. . (2025). Brown Banana Leaf (Musa x paradisiaca) Improve Betta splendens Hatching, Larvae, Survival and Growth Performance While Affecting its Sex Ratio . Borneo Journal of Resource Science and Technology, 15(2), 163–178. Retrieved from https://publisher.unimas.my/ojs/index.php/BJRST/article/view/10101