Dietary full-fat Stinkbug (Encosternum delegorguei) meal effects on growth performance, blood chemistry, liver and intestinal histology of juvenile Mozambique tilapia (Oreochromis mossambicus)

References

• Abdel-Tawwab, M., Khalil, R. H., Metwally, A. A., Shakweer, M. S., Khallaf, M. A., & Abdel-Latif, H. M. R. (2020). Effects of black soldier fly (Hermetia illucens L.) larvae meal on growth performance, organs-somatic indices, body composition, and hematobiochemical variables of European sea bass, Dicentrarchus labrax. Aquaculture 522, 735136. Article 735136. https://doi.org/10.1016/j.aquaculture.2020.735136
   Web of Science ®Google Scholar
• Adeoye, A. A., Akegbejo-Samsons, Y., Fawole, F. J., & Davies, S. J. (2020). Preliminary assessment of black soldier fly (Hermetia illucens) larval meal in the diet of African catfish (Clarias gariepinus): Impact on growth, body index, and hematological parameters. Journal of the World Aquaculture Society, 51(4), 1024–17. https://doi.org/10.1111/jwas.12691
   Web of Science ®Google Scholar
• Akinwole, A. O., Dauda, A. B., & Ogunkunle, V. O. (2020). Growth performance, nutrient utilization, survival and body indices of African catfish (Clarias gariepinus, Burchell 1822) reared on maggot meal based diet. FUDMA Journal of Sciences, 4(2), 53–59. https://doi.org/10.33003/fjs-2020-0402-109
   Google Scholar
• Alfiko, Y., Xie, D., Astuti, R. T., Wong, J., & Wang, L. (2022). Insects as a feed ingredient for fish culture: Status and trends. Aquaculture and Fisheries, 7(2), 166–178. https://doi.org/10.1016/j.aaf.2021.10.004
   Google Scholar
• Anvo, M. P. M., Aboua, B. R. D., Compaoré, I., Siaaao, R., Zoungrana-Kaboré, C. Y., Kouamelan, E. P., & Toguyéni, A. (2017). Fish meal replacement by Cirina butyrospermi caterpillar’s meal in practical diets for Clarias gariepinus fingerlings. Aquaculture Research, 48(10), 5243–5250. https://doi.org/10.1111/are.13337
   Web of Science ®Google Scholar
• AOAC International. (2003). Official methods of analysis of AOAC International (17th ed.). Gaithersburg, MD, USA, Association of Analytical Communities.
   Google Scholar
• Baeza-Arińo, R., Martĩnez-Llorens, S., Nogales-Merida, S., Jover-Cerda, M., & Tomas-Vidal, A. (2014). Study of liver and gut alterations in sea bream, Sparus aurata L., fed a mixture of vegetable protein concentrate. Aquaculture Research, 47(2), 460–471. https://doi.org/10.1111/are.12507
   Web of Science ®Google Scholar
• Belghit, I., Liland, N. S., Gjesdal, P., Biancarosa, I., Menchetti, E., Li, Y., Waagobo, R., & Krogdahl, E. L. (2018). Black soldier fly larvae meal can replace fish meal in diets of sea-water phase Atlantic salmon (Salmo salar). Aquaculture, 503, 609–619. https://doi.org/10.1016/j.aquaculture.2018.12.032
   Web of Science ®Google Scholar
• Bruni, L., Pastorelli, R., Viti, C., Gasco, L., & Parisi, G. (2018). Characterisation of the intestinal microbial communities of rainbow trout (Oncorhynchus mykiss) fed with Hermetia illucens (black soldier fly) partially defatted larva meal as partial dietary protein source. Aquaculture, 487, 56–63. https://doi.org/10.1016/j.aquaculture.2018.01.006
   Web of Science ®Google Scholar
• Cho, J., Bae, J., & Hwang, I. (2022). Effects of black soldier fly (Hermetia illucens) pre-pupae meal on the growth, stress, and immune responses of juvenile rainbow trout (Oncorhynchus mykiss) reared at different stocking densities. Aquaculture Reports, 25, Article ID 101202.
   Google Scholar
• Cho, C. Y., Slinger, S. J., & Bayley, H. S. (1982). Bioenergetics of salmonid fishes energy intake, expenditure and productivity. Comparative Biochemistry and Physiology, 73(1), 25–41. https://doi.org/10.1016/0305-0491(82)90198-5
   Google Scholar
• Coutinho, F., Castro, C., Guerreiro, I., Rangel, F., Couto, A., Serra, C. R., Peres, H., Pousão-Ferreira, P., Rawski, M., Oliva-Teles, A., & Enes, P. (2021). Mealworm larvae meal in diets for meagre juveniles: Growth, nutrient digestibility and digestive enzymes activity. Aquaculture 535, 736362. Article 736362. https://doi.org/10.1016/j.aquaculture.2021.736362
   Web of Science ®Google Scholar
• Devic, E., Leschen, W., Murray, F., & Little, D. C. (2017). Growth performance, feed utilization and body composition of advanced nursing Nile tilapia (Oreochromis niloticus) fed diets containing black soldier fly (Hermetia illucens) larvae meal. Aquaculture Nutrition, 24(1), 416–423. https://doi.org/10.1111/anu.12573
   Web of Science ®Google Scholar
• Djissou, A. S. M., Adjahouinou, D. C., Koshio, S., & Fiogbe, E. D. (2016). Complete replacement of fish meal by other animal protein sources on growth performance of Clarias gariepinus fingerlings. International Aquatic Research, 8(4), 333–341. https://doi.org/10.1007/s40071-016-0146-x
   Google Scholar
• Elia, A. C., Capucchio, M. T., Caldaroni, B., Magara, G., Dörr, A. J. M., Biasato, I., Biasibetti, E., Righetti, M., Pastorino, P., Prearo, M., Gai, F., Schiavone, A., & Gasco, L. (2018). Influence of Hermetia illucens meal dietary inclusion on the histological traits, gut mucin composition and the oxidative stress biomarkers in rainbow trout (Oncorhynchus mykiss). Aquaculture, 496, 50–57. https://doi.org/10.1016/j.aquaculture.2018.07.009
   Web of Science ®Google Scholar
• El-Sayed, A. F. M. (2020). Tilapia culture (2nd ed.). Academic Press.
   Google Scholar
• Fawole, F. J., Adeoye, A. A., Tiamiyu, L. O., Ajala, K. I., Obadara, S. O., & Ganiyu, I. O. (2020). Substituting fishmeal with Hermetia illucens in the diets of African catfish (Clarias gariepinus): Effects on growth, nutrient utilization, haemato-physiological response, and oxidative stress biomarker. Aquaculture 518, 734849. Article 734849. https://doi.org/10.1016/j.aquaculture.2019.734849
   Web of Science ®Google Scholar
• Finke, M. D. (2007). Estimate of chitin in raw whole insects. Zoo Biology, 26(2), 105–115. https://doi.org/10.1002/zoo.20123
   PubMed Web of Science ®Google Scholar
• Fischer, H., Romano, N., Renukdas, N., Kumar, V., & Sinha, A. K. (2022). Comparing black soldier fly (Hermetia illucens) larvae versus prepupae in the diets of largemouth bass, Micropterus salmoides: Effects on their growth, biochemical composition, histopathology, and gene expression. Aquaculture 546, 737323. Article 737323. https://doi.org/10.1016/j.aquaculture.2021.737323
   Web of Science ®Google Scholar
• Folch, J., Lees, M., & Stanley, G. H. S. (1957). A simple method for the isolation and purification of total lipids from animal tissues. Journal of Biological Chemistry, 226(1), 497–509. https://doi.org/10.1016/S0021-9258(18)64849-5
   PubMed Web of Science ®Google Scholar
• Gai, F., Cusimano, G. M., Maricchiolo, G., Caccamo, L., Caimi, C., Macchi, E., Meola, M., Perdichizzi, A., Tartarisco, G., & Gasco, L. (2023). Defatted black soldier fly meal in diet for grow-out gilthead seabream (Sparus aurata L. 1758): Effects on growth performance, Gill Cortisol level, digestive enzyme activities, and intestinal histological structure. Aquaculture Research, ID, 3465335. https://doi.org/10.1155/2023/3465335
   Google Scholar
• Gbai, M., Ouattara, N., Bamba, Y., Ouattara, M., Ouattara, A., & Yao, K. (2019). Substitution of the fishmeal by maggot meal in the feed of Nile tilapia Oreochromis niloticus at different stages of growth. International Journal of Fisheries and Aquaculture Research, 5(4), 25–39. . www.eajournals.org
   Google Scholar
• Guerreiro, I., Serra, C. R., Coutinho, F., Couto, A., Castro, C., Rangel, F., Pres, H., Pousão-Ferreira, P., Matos, E., Gasco, L., Gai, F., Olivia-Teles, A., & Enes, P. (2020). Digestive enzyme activity and nutrient digestibility in meagre (Argyrosomus regius) fed increasing levels of black soldier fly meal (Hermetia illucens). Aquaculture Nutrition, 27(1), 142–152. https://doi.org/10.1111/anu.13172
   Web of Science ®Google Scholar
• Gu, J., Liang, H., Ge, X., Xia, D., Pan, L., Mi, H., & Ren, M. (2022). A study of the potential effect of yellow mealworm (Tenebrio molitor) substitution for fish meal on growth, immune and antioxidant capacity in juvenile largemouth bass (Micropterus salmoides). Fish and Shellfish Immunology, 120, 214–221. https://doi.org/10.1016/j.fsi.2021.11.024
   PubMed Web of Science ®Google Scholar
• Henry, M., Gasco, L., Piccolo, G., & Fountoulaki, E. (2015). Review on the use of insects in the diet of farmed fish: Past and future. Animal Feed Science and Technology, 203, 1–22. https://doi.org/10.1016/j.anifeedsci.2015.03.001
   Web of Science ®Google Scholar
• Henry, M. A., Golomazou, E., Asimaki, A., Psofakis, P., Fountoulaki, E., Mente, E., Rumbos, C. I., Athanassiou, C. G., & Karapanagiotidis, I. T. (2022). Partial dietary fishmeal replacement with full-fat or defatted superworm (Zophobas morio) larvae meals modulates the innate immune system of gilthead seabream, Sparus aurata. Aquaculture Reports, 27, Article 101347.
   Google Scholar
• Hlophe-Ginindza, S. N., Moyo, N. A. G., & Ngambi, J. W. (2015). The effect of exogenous enzyme supplementation on growth and digestive enzyme activities in Oreochromis mossambicus fed kikuyu-based diets. Aquaculture Research, 47(12), 3777–3787. https://doi.org/10.1111/are.12828
   Web of Science ®Google Scholar
• Hua, K. (2021). A meta-analysis of the effects of replacing fish meals with insect meals on growth performance of fish. Aquaculture 530, 735732. Article 735732. https://doi.org/10.1016/j.aquaculture.2020.735732
   Web of Science ®Google Scholar
• Hu, Y., Huang, Y., Tang, T., Zhong, L., Chu, W., Dai, Z., Chen, Hu, Y., & Chen, K. (2020). Effect of partial black soldier fly (Hermetia illucens L.) larvae meal replacement of fish meal in practical diets on the growth, digestive enzyme and related gene expression for rice field eel (Monopterus albus). Aquaculture Reports 17, 100345. Article 100345. https://doi.org/10.1016/j.aqrep.2020.100345
   Web of Science ®Google Scholar
• Inje, O. F., Olufunmilayo, A. H., Audu, J. A., Ndaman, S. A., & Chidi, E. E. (2018). Protein quality of four indigenous edible insect species in Nigeria. Food Science and Human Wellness, 7(2), 175–183. https://doi.org/10.1016/j.fshw.2018.05.003
   Google Scholar
• Ishida, Y., Fujita, T., & Asai, K. (1981). New detection and separation method for amino acids by high-performance liquid chromatography. Journal of Chromatography A, 204, 143–148. https://doi.org/10.1016/S0021-9673(00)81650-7
   PubMed Web of Science ®Google Scholar
• Jabir, A. R., Razak, S. A., & Vikineswary, S. (2012). Nutritive potential and utilization of super worm (Zophobas morio) meal in the diet of Nile tilapia (Oreochromis niloticus) juvenile. African Journal of Biotechnology, 11(24), 6592–6598. https://doi.org/10.5897/AJB11.1084
   Google Scholar
• Jeong, S. M., Khosravi, S., Mauliasari, I. R., & Lee, S. M. (2020). Dietary inclusion of mealworm (Tenebrio molitor) meal as an alternative protein source in practical diets for rainbow trout (Oncorhynchus mykiss) fry. Fisheries and Aquatic Sciences, 23(1), 12. https://doi.org/10.1186/s41240-020-00158-7
   Google Scholar
• Kim, Y. S., & Ho, S. B. (2010). Intestinal goblet cells and mucins in health and disease: Recent insights and progress. Current Gastroenterology Reports, 12(5), 319–330. https://doi.org/10.1007/s11894-010-0131-2
   PubMedGoogle Scholar
• Kishawy, A. T. Y., Mohammed, H. A., Zaglool, A. W., Attia, M. S., Hassan, F. A. M., Roushdy, E. M., Ismail, T. A., & Ibrahim, D. (2022). Partial defatted black solider larvae meal as a promising strategy to replace fish meal protein in diet for Nile tilapia (Oreochromis niloticus): Performance, expression of protein and fat transporters, and cytokines related genes and economic efficiency. Aquaculture 555, 738195. Article 738195. https://doi.org/10.1016/j.aquaculture.2022.738195
   Web of Science ®Google Scholar
• Llagostera, P. F., Kallas, Z., Reig, L., & Amores de Gea, D. (2019). The use of insect meal as a sustainable feeding alternative in aquaculture: Current situation, Spanish consumers’ perceptions and willingness to pay. Journal of Cleaner Production, 229, 10–21. https://doi.org/10.1016/j.jclepro.2019.05.012
   Web of Science ®Google Scholar
• Madibana, M. J., Mwanza, M., Lewis, B. R., Fouché, C. H., Toefy, R., & Mlambo, V. (2020). Black soldier fly larvae meal as a fishmeal substitute in juvenile dusky kob diets: Effect on feed utilization, growth performance, and Blood parameters. Sustainability, 12(22), 9460. https://doi.org/10.3390/su12229460
   Web of Science ®Google Scholar
• Makkar, H. P. S., Tran, G., Heuze, V., & Ankers, P. (2014). State-of-the-art on use of insects as animal feed. Animal Feed Science and Technology, 197, 1–33. https://doi.org/10.1016/j.anifeedsci.2014.07.008
   Web of Science ®Google Scholar
• Makore, T. A., Garamumhango, P., Chirikure, T., & Chikambi, S. D. (2015). Determination of nutritional composition of Encosternum delegorguei caught in Nerumedzo community of Bikita, Zimbabwe. International Journal of Biology, 7(4), 4. https://doi.org/10.5539/ijb.v7n4p13
   Google Scholar
• Manditsera, F. A., Luning, P. A., Fogliano, V., & Lakemond, C. M. M. (2019). The contribution of wild harvested edible insects (Eulepida mashona and Henicus whellani) to nutrition security in Zimbabwe. Journal of Food Composition and Analysis, 75, 17–25. https://doi.org/10.1016/j.jfca.2018.09.013
   Web of Science ®Google Scholar
• McFadzen, I. R. B., Coombs, S. H., & Halliday, N. C. (1997). Histological indices of the nutritional condition of sardine, Sardina pilchardus (walbaum) larvae of the north coast of Spain. Journal of Experimental Marine Biology and Ecology, 212(2), 239–258. https://doi.org/10.1016/S0022-0981(96)02755-4
   Web of Science ®Google Scholar
• Mohan, K., Rajan, D. K., Muralisankar, T., Ganesan, A. R., Sathishkumar, P., & Revathi, N. (2022). Use of black soldier fly (Hermetia illucens L.) larvae meal in aquafeeds for a sustainable aquaculture industry: A review of past and future needs. Aquaculture 553, 738095. Article 738095. https://doi.org/10.1016/j.aquaculture.2022.738095
   Web of Science ®Google Scholar
• Muin, H., & Taufek, N. M. (2022). Evaluation of growth performance, feed efficiency and nutrient digestibility of red hybrid tilapia fed dietary inclusion of black soldier fly larvae (Hermetia illucens). Aquaculture and Fisheries. https://doi.org/10.1016/j.aaf.2022.09.006
   Google Scholar
• Nyuliwe, T. C., Mlambo, V., Madibana, M. J., Mwanza, M., & Wokadala, O. C. (2022). Partial substitution of fishmeal with mopane worm meal in dusky kob fingerling (Argyrosomus japonicus) diets: Feed utilization, digestive enzyme activity, Blood parameters, and growth performance. Aquaculture Journal, 2(2), 59–71. https://doi.org/10.3390/aquacj2020006
   Google Scholar
• Parmar, T. P., Kindinger, A. L., Mathieu-Resuge, M., Twining, C. W., Shipley, J. R., Kainz, M. J., & Martin-Creuzburg, D. (2022). Fatty acid composition differs between emergent aquatic and terrestrial insects-A detailed single system approach. Frontiers in Ecology and Evolution, 10. Article 952292. https://doi.org/10.3389/fevo.2022.952292
   Web of Science ®Google Scholar
• Prachom, N., Boonyoung, S., Hassaan, M. S., El-Haroun, E., & Davies, S. J. (2021). Preliminary evaluation of superworm (Zophobas morio) larval meal as a partial protein source in experimental diets for juvenile Asian sea bass, lates calcarifer. Aquaculture Nutrition, 27(5), 1-1304–1314. https://doi.org/10.1111/anu.13269
   Web of Science ®Google Scholar
• Rapatsa, M. M., & Moyo, N. A. G. (2017). Evaluation of Imbrasia belina meal as a fishmeal substitute in Oreochromis mossambicus diets: Growth performance, histological analysis and enzyme activity. Aquaculture Reports, 5, 18–26. https://doi.org/10.1016/j.aqrep.2016.11.004
   Web of Science ®Google Scholar
• Rapatsa, M. M., & Moyo, N. A. G. (2019). Enzyme activity and histological analysis of Clarias gariepinus fed on Imbrasia belina meal used for partial replacement of fishmeal. Fish Physiology and Biochemistry, 45(4), 1309–1320. https://doi.org/10.1007/s10695-019-00652-3
   PubMed Web of Science ®Google Scholar
• Rapatsa, M. M., Moyo, N. A. G. (2022). A review and meta-analysis of the effects of Replacing fishmeal with insect meals on growth of tilapias and sharptooth catfish. Aquaculture Nutrition 2022, 1–10. Article 9367587. https://doi.org/10.1155/2022/9367587
   Web of Science ®Google Scholar
• Rašković, B. S., Stanković, M. B., Marković, Z. Z., & Poleksić, V. D. (2011). Histological methods in the assessment of different feed effects on liver and intestine of fish. Journal of Agricultural Sciences, 56(1), 87–100. https://doi.org/10.2298/JAS1101087R
   Google Scholar
• Renna, M., Schiavone, A., Gai, F., Dabbou, S., Lussiana, C., Malfatto, V., Prearo, M., Capucchio, M. T., Biasato, I., Biasibetti, E., De Marco, M., Brugiapaglia, A., Zoccarato, I., & Gasco, L. (2017). Evaluation of the suitability of a partially defatted black soldier fly (Hermetia illucens L.) larvae meal as ingredient for rainbow trout (Oncorhynchus mykiss walbaum) diets. Journal of Animal Science and Biotechnology, 8(1). Article 57. https://doi.org/10.1186/s40104-017-0191-3
   Google Scholar
• Rumpold, B. A., & Schlüter, O. K. (2013). Potential and challenges of insects as an innovative source for food and feed production. Innovative Food Science and Emerging Technologies, 17, 1–11. https://doi.org/10.1016/j.ifset.2012.11.005
   Web of Science ®Google Scholar
• Sagun, S., Collins, E., Martin, C., Nolan, E. J., & Horzempa, J. (2016). Alarm odor compounds of the brown marmorated stink bug exhibit antibacterial activity. Journal of Pharmacognosy and Natural Products, 2(3), 119. https://doi.org/10.4172/2472-0992.1000119
   PubMedGoogle Scholar
• Saleh, H. H. E. (2020). Effect of feeding on fresh (wet) housefly maggots (Musca domestica) with or without Artificial diet on water Quality and growth Rates of African catfish (Clarias gariepinus Burchell, 1822) fry under laboratory conditions. Journal of Zoological Research, 2(2). https://doi.org/10.30564/jzr.v2i2.2053
   Google Scholar
• Santiago, C. B., & Lovell, R. T. (1988). Amino acid requirements for growth of Nile tilapia. Journal of Nutrition, 188(12), 1540–1546. https://doi.org/10.1093/jn/118.12.1540
   Google Scholar
• Teffo, L. S., Toms, R. B., & Eloff, J. N. (2007). Preliminary data on the nutritional composition of the composition of the edible stink-bug, ncosternum delegorguei Spinola, consumed in Limpopo province, South Africa. South African Journal of Science, 103, 434–436. https://hdl.handle.net/10520/EJC96630
   Web of Science ®Google Scholar
• Terova, G., Gini, E., Gasco, L., Moroni, F., Antonini, M., & Rimoldi, S. (2021). Effects of full replacement of dietary fishmeal with insect meal from Tenebrio molitor on rainbow trout gut and skin microbiota. Journal of Animal Science and Biotechnology, 12(1). Article 30. https://doi.org/10.1186/s40104-021-00551-9
   PubMed Web of Science ®Google Scholar
• Tippayadara, N., Dawood, M. A. O., Krutmuang, P., Hoseinifar, S. H., Doan, H. V., & Paolucci, M. (2021). Replacement of fish meal by black soldier fly (Hermetia illucens) larvae meal: Effects on growth, haematology, and skin mucus immunity of Nile tilapia, Oreochromis niloticus. Animals, 11(1), 193. https://doi.org/10.3390/ani11010193
   Web of Science ®Google Scholar
• Tran, H. Q., Prokešová, M., Zare, M., Matoušek, J., Ferrocino, I., Gasco, L., & Stejskal, V. (2022). Production performance, nutrient digestibility, serum biochemistry, fillet composition, intestinal microbiota and environmental impacts of European perch (Perca fluviatilis) fed defatted mealworm (Tenebrio molitor). Aquaculture 547, 737499. Article 737499. https://doi.org/10.1016/j.aquaculture.2021.737499
   Web of Science ®Google Scholar
• Tschirner, M., & Simon, A. (2015). Influence of different growing substrates and processing on the nutrient composition of black soldier fly larvae destined for animal feed. Journal of Insects as Food and Feed, 1(4), 249–259. https://doi.org/10.3920/JIFF2014.0008
   Web of Science ®Google Scholar
• Twining, C. W., Brenna, J. T., Lawrence, P., Shipley, J. R., Tollefson, T. N., & Winkler, D. W. (2016). Omega-3 long-chain polyunsaturated fatty acids support aerial insectivore performance more than food quantity. Proceedings of the National Academy of Sciences, 113(39), 10920–10925. https://doi.org/10.1073/pnas.1603998113
   PubMed Web of Science ®Google Scholar
• van Dyk, J. C., & Pieterse, G. M. (2008). A histo-morphological study of the testis of the sharptooth catfish (Clarias gariepinus) as reference for future toxicological assessments. Journal of Applied Ichthyology, 24(4), 415–422. https://doi.org/10.1111/j.1439-0426.2008.01127.x
   Web of Science ®Google Scholar
• van Huis, A. (2013). Potential of insects as food and feed in assuring food security. Annual Review of Entomology, 58(1), 563–583. https://doi.org/10.1146/annurev-ento-120811-153704
   PubMedGoogle Scholar
• van Huis, A. (2022). Edible insects: Challenges and prospects. Entomological Research, 52(4), 161–177. https://doi.org/10.1111/1748-5967.12582
   Web of Science ®Google Scholar
• van Soest, P. J., Robertson, J. B., & Lewis, B. A. (1991). Methods for dietary fiber, neutral detergent fiber and nonstarch polysaccharides in relation to animal nutrition. Journal of Dairy Science, 74(10), 3583–3597. https://doi.org/10.3168/jds.S0022-0302(91)78551-2
   PubMed Web of Science ®Google Scholar
• Xiao, X., Jin, P., Zheng, L., Cai, M., Yu, Z., Yu, J., & Zhang, J. (2018). Effects of black soldier fly (Hermetia illucens) larvae meal protein as a fishmeal replacement on the growth and immune index of yellow catfish (Pelteobagrus fulvidraco). Aquaculture Research, 49(4), 1–9. https://doi.org/10.1111/are.13611
   Web of Science ®Google Scholar
• Zarantoniello, M., Randazzo, B., Secci, G., Notarstefano, V., Giorgini, E., Lock, E. J., Parisi, G., & Olivotto, I. (2021). Application of laboratory methods for understanding fish responses to black soldier fly (Hermetia illucens) based diets. Journal of Insects as Food and Feed, 8(11), 1173–1195. https://doi.org/10.3920/JIFF2020.0135
   Web of Science ®Google Scholar