Main Article Content

Abstract

The effectiveness of Porphyridium cruentum, a red microalga, as an alternative live feed for black tiger shrimp (Penaeus monodon) larvae was evaluated through a series of laboratory experiments. In Experiment-1, ingestion rates were measured at the zoea-3 and mysis-2 stages with varying cell densities of P. cruentum (2,500; 5,000; and 7,500 cells/mL) over exposure periods of 1, 3, and 6 hours. Experiment-2 assessed larval performance from the nauplius stage to post larva-1 (PL-1) using P. cruentum at concentrations of 15,000; 30,000; and 45,000 cells/mL, both with and without artificial feed (AF). Experiment-3 explored the interaction of P. cruentum with certain diatom microalgae (Skeletonema costatum, Chaetoceros calcitrans, and Thalassiosira sp.) throughout the entire larval phase. All experiments employed a fully randomized design with three replications. The results showed that zoea-3 larvae had significantly higher intake rates than mysis-2. Larvae fed solely with P. cruentum at concentrations of 15,000 and 30,000 cells/mL were unable to progress to the PL-1 stage. The use of artificial feed or its combination with diatoms, particularly Thalassiosira sp., significantly (P<0.05) enhanced the larval stage index and survival rates. These findings suggest that P. cruentum is a viable complementary feed component in shrimp hatchery systems, especially when combined with other nutritional sources to improve larval performance and hatchery success.

Keywords

Black tiger shrimp Larval development Porphyridium cruentum Survival

Article Details

Author Biographies

Aninditia Sabdaningsih, Doctoral Program of Aquatic Resources Management, Department of Aquatic Resources, Faculty of Fisheries and Marine Science, Diponegoro University, Semarang-Indonesia

Doctoral Program of Aquatic Resources Management, Department of Aquatic Resources, Faculty of Fisheries and Marine Science, Diponegoro University, Semarang-Indonesia

Brata Pantjara, Research Center for Freshwater Aquaculture, National Research and Innovation Agency, Cibinong, West Java, Indonesia

Research Center for Freshwater Aquaculture, National Research and Innovation Agency, Cibinong, West Java, Indonesia

Agus Trianto, Doctoral Program of Aquatic Resources Management, Department of Aquatic Resources, Faculty of Fisheries and Marine Science, Diponegoro University, Semarang-Indonesia

Doctoral Program of Aquatic Resources Management, Department of Aquatic Resources, Faculty of Fisheries and Marine Science, Diponegoro University, Semarang-Indonesia

References

  1. Abdelhay, R.A. et al. (2025). Effect of Nitrogen Sources on Diatoms Growth and Nutritional Value for Enhancing Litopenaeus vannamei Larval Performance. Animals, 15(4), pp. 1–17. https://doi.org/10.3390/ani15040466.
  2. Amatul-samahah, A. et al. (2020). Vaccination trials against vibriosis in shrimp : A review. Aquaculture Reports, 18, p. 100471. ttps://doi.org/10.1016/j.aqrep.2020.100471.
  3. Anderson, J.L., Valderrama, D. and Jory, D. (2017). Shrimp Aquaculture Production by World Region : 2000-2017. Global Aquaculture Alliance, pp. 1–54. https://www.aquaculture alliance.org/wp-content/uploads/2018/01/ Global-Shrimp
  4. Angthong, P. et al, (2023). Shrimp microbiome and immune development in the early life stages. Developmental and Comparative Immunology 147 (2023) 104765.
  5. Ashour, M. et al. (2025). Marine Diatom Skeletonema costatum Dietary Supplementation Improves Growth, Immunological Responses, Antioxidant Activities, Gene Expressions, and Digestive Enzymes of Shrimp Litopenaeus vannamei. Aquaculture Nutrition, 2025(1). https://doi. org/10.1155/anu/5013608.
  6. Asmild, M. et al. (2024). Is economies of scale driving the development in shrimp farming from Penaeus monodon to Litopenaeus vannamei ? The case of Indonesia. 579(September 2023).
  7. Baharuddin, N.D. et al. (2024). Evaluation of diatom Halamphora sp. and harpacticoid copepod Amphiascoides neglectus as live food for black tiger shrimp Penaeus monodon postlarvae. Aquaculture, 586. https://doi.org/ 10.1016/aquaculture.40773.
  8. Balachandar, S. and Rajaram, R. (2019) ‘Influence of different diets on the growth, survival, fecundity and proximate composition of brine shrimp Artemia franciscana (Kellog, 1906). Aquaculture Research, 50(2), pp. 376–389. https://doi.org/10.1111/ are.13882.
  9. Bayu, A. et al. (2023). Biological and technical aspects on valorization of red microalgae genera Porphyridium. Biomass Conversion and Biorefinery, 13(14), pp. 12395–12411. Available at: https://doi.org/10.1007/s13399-021-02167-5.
  10. Chowdhury, A. et al. (2018). Cost–benefit analysis of ’Blue Carbon’sequestration by plantation of few key mangrove species at Sundarban Biosphere Reserve, India. Carbon … https://doi.org/10.1080/17583004.2018. 1518105.
  11. D’Souza, F.M.L. and Kelly, G.J. (2000). Effects of a diet of a nitrogen-limited alga (Tetraselmis suecica) on growth, survival and biochemical composition of tiger prawn (Penaeus semisulcatus) larvae. Aquaculture, 181(3), pp. 311–329. https://doi.org/https:// doi.org/10.1016/S0044-8486(99)00231-8.
  12. Dhanker, R. et al. (2024). Towards sustainable diatom biorefinery: Recent trends in cultivation and applications. Bioresource Technology, 391(November). https://doi.org/ 10.1016/biortech.2023.129905.
  13. Divya, M. and Aanand, S. (2020). Microalgae- A boon for larviculture of aquatic organisms. International Journal of Applied Research 2020, 6(5), pp. 138–143. https://www.allresearchjournal.com/archives/?year=2020&vol=6&issue=5&part=C&ArticleId=6692.
  14. Farhadian, O., Yusoff, F.M. and Arshad, A. (2007). Ingestion rate of postlarvae Penaeus monodon fed Apocyclops dengizicus and Artemia. Aquaculture, 269(1–4), pp. 265–270. https://doi.org/10.1016/j.aquaculture.2007.05.034.
  15. Ferreira, A.S. et al. (2021). Impact of growth medium salinity on galactoxylan exopolysaccharides of Porphyridium purpureum. Algal Research, 59. https://doi.org/10.1016/j.algal.2021.102439.
  16. Gui, L. et al. (2022) ‘Carotenoid-rich microalgae promote growth and health conditions of Artemia nauplii’, Aquaculture, 546(August). Available at: https://doi.org/10.1016/j.aquaculture.2021.737289.
  17. Hernández-Sandoval, F.E. et al. (2022) ‘Effects on Cell Growth, Lipid and Biochemical Composition of Thalassiosira weissflogii (Bacillariophyceae) Cultured under Two Nitrogen Sources’, Applied Sciences (Switzerland), 12(3), pp. 1–11. Available at: https://doi.org/10.3390/app12030961.
  18. Jamali, H., Ahmadifard, N. and Abdollahi, D. (2015) ‘Evaluation of growth, survival and body composition of larval white shrimp (Litopenaeus vannamei) fed the combination of three types of algae’, International Aquatic Research, 7(2), pp. 115–122. Available at: https://doi.org/10.1007/s40071-015-0095-9.
  19. Jaseera, K.. et al. (2021) ‘Dietary supplementation of microalgae, Aurantiochytrium sp. and co-feeding with Artemia enhances the growth, stress tolerance and survival in Penaeus monodon (Fabricius, 1798) post larvae’, Aquaculture, 533(November). https://doi.org/10.1016/ j.aquaculture.2020.736176.
  20. De Jesus Raposo, M.F., De Morais, R.M.S.C. and De Morais, A.M.M.B. (2013) ‘Bioactivity and applications of sulphated polysaccharides from marine microalgae’, Marine Drugs. MDPI AG, pp. 233–252. Available at: https://doi.org/10.3390/md11010233.
  21. Kannukkarathi, T. et al. (2025) ‘Growth and health benefits of marine picoalga Picochlorum maculatum MACC3-based feed formulations to black tiger shrimp (Penaeus monodon) post-larvae’, Journal of Applied Phycology. https://doi.org/10.1007/s10811-025-03556-3.
  22. Khumngern, T. et al. (2025) ‘Optimizing growth and pigment content of promising green microalgae and application of living microalgal cells as a sole practical diet for white shrimp larvae’, Journal of Applied Biology and Biotechnology, 13(3), pp. 58–70. https://doi.org/10.7324/JABB.2025.211147.
  23. Kiatmetha, P. et al. (2011) ‘Enhancement of survival and metamorphosis rates of Penaeus monodon larvae by feeding with the diatom Thalassiosira weissflogii’, Aquaculture International, 19(4). https://doi.org/10.1007/ s10499- 010-9375-y.
  24. Kim, S.H. et al. (2021) ‘Improvement of unsaturated fatty acid production from porphyridium cruentum using a two-phase culture system in a photobioreactor with light-emitting diodes (leds)’, Journal of Microbiology and Biotechnology, 31(3). https://doi.org/10.4014/JMB.2011.11004.
  25. Kumlu, M and Kumlu, Metin (1998) Larval Growth and Survival of Penaeus Indicus (Decapoda: Penaeidae) On Live Feeds.
  26. Lavens, P. and Sorgeloos, P. (2000) ‘Experiences on importance of diet for shrimp postlarval quality’, Aquaculture, 191(1–3), pp. 169–176.https://doi.org/10.1016/S0044-8486(00)00426-9.
  27. Liberti, D. et al. (2023) ‘Shedding Light on the Hidden Benefit of Porphyridium cruentum Culture’, Antioxidants, 12(2). https://doi.org/ 10.3390/antiox12020337.
  28. Mai, T.D. et al. (2021) ‘Fatty Acid Profiles of Selected Microalgae Used as Live Feeds for Shrimp Postlarvae in Vietnam’, Aquaculture Journal, 1(1), pp. 26–38. https://doi.org/ 10.3390/aquacj1010004.
  29. Martínez Soler, M. et al. (2023a) ‘Effect of HUFA in Enriched Artemia on Growth Performance, Biochemical and Fatty Acid Content, and Hepatopancreatic Features of Penaeus vannamei Postlarvae from a Commercial Shrimp Hatchery in Santa Elena, Ecuador’, Aquaculture Nutrition, 2023. https://doi.org/10.1155/2023/7343070.
  30. Martínez Soler, M. et al. (2023b) ‘Effect of HUFA in Enriched Artemia on Growth Performance, Biochemical and Fatty Acid Content, and Hepatopancreatic Features of Penaeus vannamei Postlarvae from a Commercial Shrimp Hatchery in Santa Elena, Ecuador’, Aquaculture Nutrition, 2023. https://doi.org/10.1155/2023/7343070.
  31. Millán-Almaraz, M.I. et al. (2021) ‘Effect of light and feed density on ingestion rate, protein and lipid content of Artemia franciscana juveniles’, Latin American Journal of Aquatic Research, 49(5), pp. 717–724.https://doi.org/10.3856/vol49-issue5-fulltext-2695.
  32. de Moraes, L.B.S. et al. (2022) ‘Microalgae for feeding of penaeid shrimp larvae: an overview’, Aquaculture International, 30(3), pp. 1295–1313. https://doi.org/10.1007/ s10499-022-00857-z.
  33. Nauta, R.W. et al. (2025) ‘Co-Culture of Gracilariopsis longissima Seaweed and Penaeus monodon Shrimp for Environmental and Economic Resilience in Poor South-East Asian Coastal Aquaculture Communities’, Sustainability (Switzerland), 17(9), pp. 1–16. https://doi.org/10.3390/su17093910.
  34. Pantjara, B. et al. (2024) ‘Juvenile production technology for tiger shrimp , Penaeus monodon , through different stocking density using a recirculation system’, (December 2023), pp. 1–14. https://doi.org/10.1111/ jwas.13055.
  35. Piña, P. et al. (2006) ‘Survival, development and growth of the Pacific white shrimp Litopenaeus vannamei protozoea larvae, fed with monoalgal and mixed diets’, Aquaculture, 253(1–4), pp. 523–530. https://doi.org/10.1016/ J.Aquaculture.2005.07.016.
  36. Safi, C. et al. (2013) ‘Evaluation of the protein quality of Porphyridium cruentum’, Journal of Applied Phycology, pp. 497–501. https://doi.org/10.1007/s10811-012-9883-4.
  37. Samat, N.A. et al. (2020) ‘Enhancement of live food nutritional status with essential nutrients for improving aquatic animal health: A review’, Animals. https://www.mdpi. com/ 932190.
  38. Rajamanickam R. et al. (2025). Microalgae-based nutritional supplements: Sustainable applications for high-nutritional-value food production. Process Biochemistry 157 (2025) 162–182
  39. Samat, N.A. et al. (2021) ‘The efficacy of Moina Micrura enriched with probiotic bacillus pocheonensis in enhancing survival and disease resistance of red hybrid tilapia (Oreochromis spp.) Larvae’, Antibiotics, 10(8). Available at: https://doi.org/10.3390/ antibiotics10080989.
  40. Sharma, T. et al. (2025) ‘Microalgae as an emerging alternative raw material of docosahexaenoic acid and eicosapentaenoic acid–a review’, Critical Reviews in Food Science and Nutrition [Preprint]. Available at: https://doi.org/10.1080/10408398.2025.2486267.
  41. Soto-Sánchez, O. et al. (2023) ‘Microalgae as Raw Materials for Aquafeeds: Growth Kinetics and Improvement Strategies of Polyunsaturated Fatty Acids Production’, Aquaculture Nutrition, 2023. Available at: https://doi.org/10.1155/2023/5110281.
  42. Supriyadi, H. et al. (2017) ‘Prevalensi infeksi white spot syndrome virus (WSSV) pada induk udang windu (Penaeus monodon) hasil tangkapan dari alam’, Jurnal Penelitian Perikanan Indonesia, 11(5), p. 69. Available at: https://doi.org/10.15578/jppi.11.5.2005.69-73.
  43. Suresh, A. et al. (2025) ‘Microalgae as a source of antimicrobial compounds : A review of bioactive metabolites and their therapeutic potentials’, 2(2), pp. 43–64.
  44. Tang, Y. et al. (2020) ‘Effects of live microalgae and algae powder on microbial community, survival, metamorphosis and digestive enzyme activity of Penaeus monodon larvae at different growth stages’, Aquaculture, 526. https://doi.org/10.1016/ j.aquaculture.2020.735344.
  45. Torres-Bayona, C. et al. (2023) ‘Microalgae and Cyanobacteria, a Promising Source of Antimicrobial Molecules Against Aquatic Pathogen’, Turkish Journal of Fisheries and Aquatic Sciences, 23(2). https://doi.org/ 10.4194/ TRJFAS21184.
  46. Zhao, M. et al. (2020a) ‘Effects of ammonia on shrimp physiology and immunity: a review’, Reviews in Aquaculture, 12(4), pp. 2194–2211. https://doi.org/10.1111/raq.12429.
  47. Zhao, M. et al. (2020b) ‘Effects of ammonia on shrimp physiology and immunity: a review’,