FAO. The Global Status of Seaweed Production, Trade and Utilization. Globefish Research Programme Vol. 124, 120 (FAO, 2018).
Tacon, A. G. Trends in global aquaculture and aquafeed production: 2000–2017. Rev. Fish. Sci. Aquacult. 28(1), 43–56 (2020).
Mude, J. N. & Ravuru, D. B. Growth of cultured White leg shrimp Litopenaeus vannamei (Boone, 1931) of brackish water culture system in winter season with artificial diet. J. Aquacult. Res. Dev. 6(2), 1–10 (2015).
FAO. El Estado Mundial de la Pesca y la Acuicultura 2020. Versión Resumida. La Sostenibilidad en Acción. (FAO, 2020). ISBN 978-92-5-132756-2.
Briggs, M., Funge-Smith, S., Subasinghe, R. & Phillips, M. 2004. Introduction and movement of Penaeus vannamei and Penaeus stylorostris in Asia and the Pacific. Food and Agriculture Organization of the United Nations. http://www.fao.org/3/ad505e/ad505e00.htm#Contents. Accessed 3rd May 2020.
Ravuru, D. B. & Mude, J. N. Growth of cultured white leg shrimp Litopenaeus vannamei (Boone, 1931) of brackish water culture system in summer season with artificial diet. Adv. Appl. Sci. Res. 5(2), 25–28 (2014).
Jannathulla, R., Dayal, J. S., Ambasankar, K., Thulasi, D. & Vasantha, D. Carcass amino acid, fatty acid and mineral composition of Penaeus vannamei Boone, 1931 fed diets with fermented oilseed meals/cakes. Int. J. Fish. Aquat. Stud. 6(6), 233–240 (2018).
Thitamadee, S. et al. Review of current disease threats for cultivated penaeid shrimp in Asia. Aquaculture 452, 69–87 (2016).
Wyban, J. Selective breeding of Penaeus vannamei: Impact on world aquaculture and lessons for future. in: BRAQCON 2019: World Brackishwater Aquaculture Conference. Journal of Coastal Research, Special Issue No. 86, 1–5 (eds Jithendran, K. P. et al.) (Coconut Creek, 2019). ISSN 0749-0208.
Ottinger, M., Clauss, K. & Kuenzer, C. Aquaculture: Relevance, distribution, impacts and spatial assessments: A review. Ocean Coast. Manag. 119, 244–266 (2016).
Tran, L. et al. Determination of the infectious nature of the agent of acute hepatopancreatic necrosis syndrome affecting penaeid shrimp. Dis. Aquat. Organ. 105, 45–55. https://doi.org/10.3354/dao02621 (2013).
Holt, C. C., Bass, D., Stentiford, G. D. & van der Giezen, M. Understanding the role of the shrimp gut microbiome in health and disease. J. Inverteb. Pathol. 1, 107387 (2020).
Peña-Navarro, N., Castro-Vásquez, R., Vargas-Leitón, B. & Dolz, G. Molecular detection of acute hepatopancreatic necrosis disease (AHPND) in Penaeus vannamei shrimps in Costa Rica. Aquaculture 1, 735190 (2020).
Jha, R. K. et al. Efficacy of natural herbal formulation against acute hepatopancreatic necrosis disease (AHPND) causing Vibrio parahaemolyticus in Penaeus vannamei. Vet. Med. Open J 2(1), 1–6 (2016).
Dabu, I. M. et al. The first record of acute hepatopancreatic necrosis disease in the Philippines. Aquacult. Res. 48(3), 792–799 (2017).
Dang, L. T., Nguyen, H. T., Hoang, H. H., Lai, H. N. & Nguyen, H. T. Efficacy of rose myrtle rhodomyrtus tomentosa seed extract against acute hepatopancreatic necrosis disease in pacific whiteleg shrimp Penaeus vannamei. J. Aquat. Anim. Health. 31, 311–319 (2019).
Muthukrishnan, S. et al. Vibrio parahaemolyticus and Vibrio harveyi causing acute hepatopancreatic necrosis disease (AHPND) in Penaeus vannamei (Boone, 1931) isolated from Malaysian shrimp ponds. Aquaculture 511, 734227. https://doi.org/10.1016/j.aquaculture.2019.734227 (2019).
Sotomayor, M. A. et al. Efficacy assessment of commercially available natural products and antibiotics, commonly used for mitigation of pathogenic Vibrio outbreaks in Ecuadorian Penaeus (Litopenaeus) vannamei hatcheries. PLoS ONE 14(1), e0210478. https://doi.org/10.1371/journal.pone.0210478 (2019).
Chen, H. et al. Tissue distribution, bioaccumulation characteristics, and health risk of antibiotics in cultured fish from a typical aquaculture area. J. Hazard Mater. 343, 140–148. https://doi.org/10.1016/j.jhazmat.2017.09.017 (2018).
Vinay, T. N. et al. Vibrio harveyi biofilm as immunostimulant candidate for high-health pacific white shrimp, Penaeus vannamei farming. Fish Shellfish Immunol. 95, 498–505 (2019).
Tsai, C. Y. et al. LpxD gene knockout elicits protection to Litopenaeus vannamei, white shrimp, against Vibrio parahaemolyticus infection. Aquacult. Int. 27(5), 1383–1393 (2019).
Liu, X., Steele, J. C. & Meng, X. Z. Usage, residue, and human health risk of antibiotics in Chinese aquaculture: A review. Environ. Pollut. 223, 161–169 (2017).
Dawood, M. A. O., Koshio, S., Abdel-Daim, M. M. & Van Doan, H. Probiotic application for sustainable aquaculture. Rev. Aquac. 11(3), 907–924 (2019).
Dawood, M. A. O. & Koshio, S. Recent advances in the role of probiotics and prebiotics in carp aquaculture: A review. Aquaculture. 454, 243–251 (2016).
Adel, M., Yeganeh, S., Dawood, M. A. O., Safari, R. & Radhakrishnan, S. Effects of Pediococcus pentosaceus supplementation on growth performance, intestinal microflora, and disease resistance of white shrimp, Litopenaeus vannamei. Aquacult. Nutr. 23(6), 1401–1409 (2017).
Situmorang, M. L. et al. Poly-β-hydroxybutyrate (PHB) improves nursery-phase pacific white shrimp Litopenaeus vannamei defense against vibriosis. N. Am. J. Aquacult. 82(1), 108–114 (2020).
Manju, S., Malaikozhundan, B., Withyachumnarnkul, B. & Vaseeharan, B. Essential oils of Nigella sativa protects Artemia from the pathogenic effect of Vibrio parahaemolyticus Dahv2. J. Inverteb. Pathol. 136, 43–49. https://doi.org/10.1016/j.jip.2016.03.004 (2016).
Peng, B. et al. Identification of polyvalent protective immunogens from outer membrane proteins in Vibrio parahaemolyticus to protect fish against bacterial infection. Fish Shellfish Immunol. 54, 204–230. https://doi.org/10.1016/j.fsi.2016.04.012 (2016).
Bulfon, C., Galeotti, M. & Volpatti, D. Medicinal plant extracts modulate respiratory burst and proliferation activity of rainbow trout (Oncorhynchus mykiss) leukocytes. Fish Physiol. Biochem. 44, 109–117. https://doi.org/10.1007/s10695-017-0417-5 (2017).
Kumaran, T., Thanga Viji, V., Velmurugan, S. & Citarasu, T. Influence of selected antiviral herbal active principals against shrimp White Spot Syndrome virus (WSSV). Int. J. Mol. Biol. Biochem. 2(1), 41–49 (2014).
Maldonado-Garcia, M. et al. Antioxidant and immunostimulant potentials of Chenopodium ambrosioides Lin Pacific red snapper (Lutjanus peru). Aquaculture 513, 734414. https://doi.org/10.1016/j.aquaculture.2019.734414 (2019).
Shabana, M. S., Karthika, M. & Ramasubramanian, V. Effect of dietry Citrus sinensis peel extract on growth performance, digestive enzyme activity, muscle biochemical composition, and metabolic enzyme status of the freshwater fish, Catla catla. J. Basic Appl. Zool. 80, 51. https://doi.org/10.1186/s41936-019-0119-x (2019).
McClatchey, W. From Polynesian healer to health food stores: Changing perspectives of Morinda citrifolia (Rubiaceae). Integrat. Cancer Ther. 1(2), 110–120. https://doi.org/10.1177/1534735402001002002 (2002).
Nerurkar, P., Hwang, P. W. & Saksa, E. Anti-diabetic potential of Noni: The Yin and the Yang. Molecules 20, 17684–17719. https://doi.org/10.3390/molecules201017684 (2015).
Nerurkar, P., Hwang, P. W. & Saksa, E. The effect of Morinda citrifolia L. fruit juice on the blood sugar level and other serum parameters in patients with diabetes type 2. Evid. Based Complement. Altern. Med. 20, 3565427. https://doi.org/10.1155/2018/3565427 (2015).
Kustiarini, D. A., Nishigaki, T., Kanno, H. & To, H. Effects of Morinda citrifolia on rheumatoid arthritis in SKG mice. Biol. Pharm. Bull. 42, 496–500. https://doi.org/10.1248/bpb.b18-00480 (2019).
Zhang, W. et al. Antibacterial constituents of Hainan Morinda citrifolia (Noni) leaves. J. Food Sci. 81(5), M1192–M1196. https://doi.org/10.1111/1750-3841.13302 (2016).
Sibi, G., Chatly, P., Adhikari, S. & Ravikumar, K. R. Phytoconstituents and their influence on antimicrobial properties of Morinda citrifolia L. Res. J. Med. Plants 6(6), 441–448. https://doi.org/10.3923/RJMP.2012.441.448 (2012).
Halim, A. M. & Prajitno, A. Aqueous Morinda citrifolia leaves extract enhancing glutathione peroxidase activity and α2-macroglobulin gene expression and Macrobrachium rosenbergii. Res. J. Life Sci. https://doi.org/10.21776/ub.rjls.2017.004.01.4 (2017).
Rodríguez, M. G. A., León, J. A. R., Borbor, C. L. D., Beltrán, C. N. T. & Orrala, R. M. M. Immunomodulatory and anti-vibrio properties of plant extract to manage the health of the shrimp Penaeus vannamei. AquaTech. Rev. Iberoam. Acuicult. 4(2), 109–123 (2022).
Chang, Y. H., Kuo, W. C., Wang, H. C. & Chen, Y. M. Biocontrol of acute hepatopancreatic necrosis disease (AHPND) in shrimp using a microalgal-bacterial consortium. Aquaculture 521, 734990 (2020).
Lin, H., Li, Z., Chen, Y., Zheng, W. & Yang, K. Effect of dietary traditional Chinese medicines on apparent digestibility coefficient of nutrients for white shrimp Litopenaeus vannamei, Boone. Aquaculture 253, 495–501. https://doi.org/10.1016/j.aquaculture.2004.11.048 (2006).
Zahran, E., Risha, E., AbdelHamid, F., Mahgoub, H. A. & Ibrahim, T. Effects of dietary Astragalus polysaccharides (APS) on growth performance, immunological parameters, digestive enzymes, and intestinal morphology of Nile tilapia (Oreochromis niloticus). Fish Shellfish Immunol. 38(1), 149–157. https://doi.org/10.1016/j.fsi.2014.03.002 (2014).
Gabriel, N. N., Qiang, J., Ma, X. Y., Xu, P. & Nakwaya, D. N. Effects of dietary Aloe vera crude extracts on digestive enzyme activities and muscle proximate composition of GIFT tilapia juveniles. S. Afr. J. Anim. Sci. 47(6), 904–913. https://doi.org/10.4314/sajas.v47i6.18 (2017).
Li, Z. et al. Growth performance, digestive enzyme activities and serum nonspecific immunity of the red tilapia (Oreochromis mossambicus × Oreochromis niloticus) fed diets supplemented with ultrafine powder of Enteromopha prolifera*. J. Oceanol. Limnol. 36(5), 1843–1850. https://doi.org/10.1007/s00343-018-7142-5 (2018).
Liu, X. et al. The effect of dietary Panax ginseng polysaccharide extract on the immune responses in white shrimp, Litopenaeus vannamei. Fish Shellfish Immunol. 30(20), 495–500. https://doi.org/10.1016/j.fsi.2010.11.018 (2011).
Wu, C. et al. Dietary administration of Gynura bicolor (Roxb. Willd) DC water extract enhances immune response and survival rate against Vibrio alginolyticus and white spot syndrome virus in white shirmp Litopenaeus vannamei. Fish Shellfish Immunol. 42(1), 25–33. https://doi.org/10.1016/j.fsi.2014.10.016 (2015).
Moh, J. H. Z. et al. Effect of Noni, Morinda citrifolia fruit extract supplementation on the growth performances and physiological responses of the hepatopancreas of Whiteleg shrimp Penaeus vannamei post larvae. Aquacult. Rep. 21, 100798. https://doi.org/10.1016/j.aqrep.2021.100798 (2021).
Natheer, E. S., Sekar, C., Amutharaj, P., Syed Abdul Rahman, M. & Feroz Khan, K. Evaluation of antibacterial activity of Morinda citrifolia, Vitex trifolia and Chromolaena odorata. Afr. J. Pharm. Pharmacol. 6(11), 783–788. https://doi.org/10.5897/AJPP11.435 (2012).
Hong, X. P., Xu, D., Zhuo, Y., Liu, H. Q. & Lu, L. Q. Identification and pathogenicity of Vibrio parahaemolyticus isolates and immune response of Penaeus (Litopenaeus) vannamei (Boone). J. Fish Dis. 39(9), 1085–1097 (2016).
Anirudhan, A. et al. Pandanus tectorius fruit extract promotes Hsp70 accumulation, immune-related gene expression and Vibrio parahaemolyticus tolerance in the white-leg shrimp Penaeus vannamei. Fish Shellfish Immunol. 109, 97–105 (2021).
Manan, H., Moh, J. H. Z., Othman, F. & Ikhwanuddin, M. Histopathology of the hepatopancreas of Pacific White Shrimp, Penaeus vannamei from none early mortality syndrome (EMS) shrimp ponds. J. Fish. Aquat. Sci. 10(6), 562–568. https://doi.org/10.3923/jfas.2015.562.568 (2015).
Citarasu, T., Sivaram, V., Immanuel, G., Rout, N. & Murugan, V. Influence of selected Indian immunostimulant herbs against white spot syndrome virus (WSSV) infection in black tiger shrimp, Penaeus monodon with reference to hematological, biochemical and immunological changes. Fish Shellfish Immunol. 21, 372–384. https://doi.org/10.1016/j.fsi.2006.01.002 (2006).
Chotigeat, W., Tongsupa, S., Supamataya, K. & Phongdara, A. Effect of Fucoidan on diseases resistance of Black Tiger Shrimp. Aquaculture 233, 23–30. https://doi.org/10.1016/j.aquaculture.2003.09.025 (2004).
Kongchum, P., Chimtong, S., Chareansak, N. & Subprasert, P. Effect of green tea extract on Vibrio parahaemolyticus inhibition in pacific white shrimp (Litopenaeus vannamei) postlarvae. Agric. Agric. Sci. Procedia 11, 117–124. https://doi.org/10.1016/j.aaspro.2016.12.020 (2016).
Chakraborty, S. B. & Hancz, C. Application of phytochemicals as immunostimulant, antipathogenic and antistress agents in finfish culture. Rev. Aquacult. 3, 103–119. https://doi.org/10.1111/j.1753-5131.2011.01048.x (2011).
Deaton, J. Enzymes and Probiotics for Immune Health. (2018). https://www.deerland.com/chew/enzymes-and-probiotics-for-immune-health/. Accessed 20 Sept 2019.
Zokaeifar, H. et al. Effects of Bacillus subtilis on the growth performance, digestive enzymes, immune gene expression and disease resistance of white shrimp, Litopenaeus vannamei. Fish Shellfish Immunol. 33, 683–689. https://doi.org/10.1016/j.fsi.2012.05.027 (2012).
Patel, S. A critical review on serine protease: Key immune manipulator and pathology mediator. Allergol. Immunopathol. 45(6), 579–591. https://doi.org/10.1016/j.aller.2016.10.011 (2017).
Li, C. et al. Trypsin in Litopenaeus vannamei is required for the generation of hemocyanin-derived peptides. Dev. Comp. Immunol. 79, 95–104. https://doi.org/10.1016/j.dci.2017.10.015 (2017).
Xu, D. et al. Dietary glutathione as an antioxidant improves resistance to ammonia exposure in Litopenaeus vannamei. Aquacult. Res. 43(2), 311–316. https://doi.org/10.1111/j.1365-2109.2011.02820.x (2012).
De La Fuente, M. & Victor, V. M. Antioxidants as modulators of immune function. Immunol. Cell Biol. 78(1), 49–54. https://doi.org/10.1046/j.1440-1711.2000.00884.x (2000).
Olguín-León, P., Enríquez-Espinoza, T., Mendoza-Cano, F., Encinas-García, T. & Sánchez-Paz, A. Transcriptional profile of pyruvate kinase and pancreatic lipase encoding mRNAs of the Pacific whiteleg shrimp Penaeus vannamei during PstDV-1 infection. Aquacult. Res. https://doi.org/10.1111/are.13380.10.1111/ARE.13380 (2017).
Javahery, S., Noori, A. & Hoseinifar, S. H. Growth performance, immune response and digestive enzyme activity in Pacific white shrimp, Penaeus vannamei Boone, 1931, fed dietary microbial lysozyme. Fish Shellfish Immunol. 92, 528–535. https://doi.org/10.1016/j.fsi.2019.06.049 (2019).
Schleder, D. D. et al. Effect of brown seaweeds on Pacific white shrimp growth performance, gut morphology, digestive enzymes activity and resistance to white spot virus. Aquaculture 495, 359–365. https://doi.org/10.1016/j.aquaculture.2018.06.020 (2018).
Chatterton, R. T. Jr., Vogelsong, K. M., Lu, Y., Ellman, A. B. & Hudgens, G. A. Salivary α-amylase as a measure of endogenous adrenergic activity. Clin. Physiol. 16(4), 433–448. https://doi.org/10.1111/j.1475-097X.1996.tb00731.x (1996).
Pacheco, R., Ascencio, F., Zarain, M., Gómez, G. & Campa, Á. Enhancement of superoxide dismutase and catalase activities in juvenile brown shrimp, Farfantepenaeus californiensis (Holmes, 1900), fed -1,3 glucan vitamin E, and β-carotene and infected with white spot syndrome virus. Latin Am. J. Aquat. Res. 39(3), 534–543. https://doi.org/10.4067/S0718-560X2011000300013 (2011).
Yeh, S. & Chen, J. White shrimp Litopenaeus vannamei that received the hot-water extract of Gracilaria tenuistipitata showed earlier recovery in immunity after a Vibrio alginolyticus injection. Fish Shellfish Immunol. 26(5), 724–730. https://doi.org/10.1016/j.fsi.2009.02.025 (2009).
Kaleo, I. V. et al. Effects of Moringa oleifera leaf extract on growth performance, physiological an immune response, and related immune gene expression of Macrobrachium rosenbergii with V. anguillarium and ammonia stress. Fish Shellfish Immunol. 89, 603–613. https://doi.org/10.1016/j.fsi.2019.03.039 (2019).
Mercier, L. et al. Metabolic and immune responses in Pacific whiteleg shrimp Litopenaeus vannamei exposed to a repeated handling stress. Aquaculture 258(1–4), 633–640. https://doi.org/10.1016/j.aquaculture.2006.04.036 (2006).
Vergauwen, B., Pauwels, F. & van Beeumen, J. J. Glutathione and catalase provide overlapping defense for protection against respiration-generated hydrogen peroxide in Haemophilus influenzae. J. Bacteriol. 185(18), 5555–5562. https://doi.org/10.1128/JB.185.18.5555-5562.2003 (2003).
Boudet, L. N. C. et al. Histopathological and biochemical evidence of hepatopancreatic toxicity caused by cadmium in white shrimp, Palaemonetes argentines. Ecotoxicol. Environ. Saf. 113, 231–240. https://doi.org/10.1016/j.ecoenv.2014.11.019 (2015).
Chen, K. et al. Evaluation of different lipid sources in diet of pacific white shrimp Litopenaeus vannamei at low salinity. Aquacult. Rep. 2, 163–168. https://doi.org/10.1016/j.aqrep.2015.10.003 (2015).
Johnston, D. J., Calvert, K. A., Crear, B. J. & Carter, C. G. Dietary carbohydrate/lipid ratios and nutritional condition in juvenile southern rock lobster, Jasus edwardsii. Aquaculture 220(1–4), 667–682. https://doi.org/10.1016/S0044-8486(02)00562-8 (2003).
Bhavan, P. S. & Geraldine, P. Histopathology of the hepatopancreas and gills of the prawn Macrobrachium malcolmsonii exposed to endosulfan. Aquat. Toxicol. 50(4), 331–339. https://doi.org/10.1016/S0166-445X(00)00096-5 (2000).
Wu, J., Chen, H. & Huang, D. Histopathological and biochemical evidence of hepatopancreatic toxicity caused by cadmium and zinc in the white shrimp, Litopenaeus vannamei. Chemosphere 73, 1019–1026. https://doi.org/10.1016/j.chemosphere.2008.08.019 (2008).
Ribeiro, K., Papa, L. P., Vicentini, C. A. & Franceschini-Vicentini, I. B. The ultrastructural evaluation of digestive cells in the hepatopancreas of Amazon River prawn, Macrobrachium amazonicum. Aquacult. Res. 47(4), 1251–1259. https://doi.org/10.1111/are.12582 (2016).
Franceschini-Vicentini, I. B. et al. Histoarchitectural features of the hepatopancreas of the Amazon River prawn Macrobrachium amazonicum. Int. J. Morphol. 27(1), 121–128. https://doi.org/10.4067/S0717-95022009000100022 (2009).
Khimmakthong, U. & Sukkarun, P. The spread of Vibrio parahaemolyticus in tissues of the Pacific white shrimp Litopenaeus vannamei analyzed by PCR and histopathology. Microb. Pathog. 113, 107–112. https://doi.org/10.1016/j.micpath.2017.10.028 (2017).
Velazquez-Lizarraga, A. E. et al. Transcriptomic analysis of Pacific White shrimp (Litopenaeus vannamei, Boone 1931) in response to acute hepatopancreatic necrosis disease caused by Vibrio parahaemolyticus. PLoS ONE 14(8), e0220993. https://doi.org/10.1371/journal.pone.0220993 (2019).
Nadella, R. K. et al. Histopathological changes in giant freshwater prawn Macrobrachium rosenbergii (de Man 1879) fed with probiotic Bacillus licheniformis upon challenge with Vibrio alginolyticus. Aquacult. Res. 49, 81–92. https://doi.org/10.1111/are.13436 (2017).
Jiravanichpaisal, P., Miyazaki, T. & Limsuwan, C. Histopathology, biochemistry and pathogenicity of Vibrio harveyi infecting black tiger prawn Penaeus monodon. J. Aquat. Anim. Health 6(1), 27–35. https://doi.org/10.1577/1548-8667(1994)006%3c0027:HBAPOV%3e2.3.CO;2 (1994).
Saptiani, G., Prayitno, S. B., Anggoro, S. & Pebrianto, C. A. The influence of Acanthus ilicifolius extracts to histopathological on hepatopancreas of tiger shrimp (Penaeus monodon F.). Int. J. Mar. Aquat. Resourc. Convserv. Coexist. 2(1), 1–6 (2017).
Pope, E. C. et al. Enhanced cellular immunity in shrimp (Litopenaeus vannamei) after ‘vaccination’. PLoS ONE 6(6), e20960. https://doi.org/10.1371/journal.pone.0020960 (2011).
Jiravanichpaisal, P., Lee, B. L. & Soderhall, K. Cell-mediated immunity in arthropods: Hematopoiesis, coagulation, melanization and opsonization. Immunobiology 211(4), 213–236. https://doi.org/10.1016/j.imbio.2005.10.015 (2006).
Barreda, D. R. & Belosevic, M. Transcriptional regulation of hemopoiesis. Dev. Comp. Immunol. 25(8–9), 763–789. https://doi.org/10.1016/S0145-305X(01)00035-0 (2001).
Jiravanichpaisal, P., Bangyeekhun, E., Soderhall, K. & Soderhall, I. Experimental infection of white spot syndrome virus in freshwater crayfish Pacifastacus leniusculus. Dis. Aquat. Organ. 47, 151–157. https://doi.org/10.3354/dao047151 (2001).
Soderhall, I., Bangyeekhun, E., Mayo, S. & Soderhall, K. Hemocyte production and maturation in an invertebrate animal; proliferation and gene expression in hematopoietic stem cells of Pacifastacus leniusculus. Dev. Comp. Immunol. 27(8), 661–672. https://doi.org/10.1016/S0145-305X(03)00039-9 (2003).
Sreeram, M. P. & Menon, N. R. Histopathological changes in the hepatopancreas of the penaeid shrimp Metapenaeus dobsoni exposed to petroleum hydrocarbons. J. Mar. Biol. Assoc. India 47(2), 160–168 (2005).
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