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Differences in Life History Traits and Morphology in Wild vs. Domesticated Populations of Black Soldier Fly, Hermetia illucens (Diptera: Stratiomyidae)

Received: 26 July 2022     Accepted: 12 August 2022     Published: 6 June 2023
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Abstract

The Black Soldier Fly (BSF) Hermetia illucens is widely studied as a sustainable alternative source of protein. Herein, we evaluated the changes in life history and morphometric traits between wild (WP) and domesticated populations (DP) with implications for larval biomass production. Prepupa stages of both populations were maintained under the same rearing conditions from July 2020 to June 2021. Our results show that the pupation time was longer in WP (10.25 ± 2.66 days) than in DP (7.2 ± 1.1 days). In contrast, the emergence time of BSF adults was shorter in WP (8.3 ± 2.2 days) than in DP (9.7 ± 1.8 days). The courtship was nearly similar in both populations. Mounting and reverse coupling were the two different copulation models used by BSF adults in WP while reverse coupling dominated in DP. The BSF females laid more eggs in WP (1468.75 ± 593.09 eggs) than in DP (246.21 ± 96.23 eggs). The egg stage was similar in length and width in both populations while the morphometric traits in the larval, pupal and adult stages were consistently lower in domesticated than in wild population. The life span of adults (males and females) was longer in DP than in WP. Our findings indicate higher values of morphological traits in WP than in DP, and distinct mating and reproductive behaviours between both populations. Our results suggest ‘domestication syndrome hypothesis’ as the main cause of changes in reproductive behaviour and reduction of size in DP. Therefore, wild population of H. illucens seems be more suitable for maggot mass production as an alternative source of protein for animal feed production.

Published in Animal and Veterinary Sciences (Volume 11, Issue 3)
DOI 10.11648/j.avs.20231103.13
Page(s) 71-79
Creative Commons

This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited.

Copyright

Copyright © The Author(s), 2023. Published by Science Publishing Group

Keywords

Black Soldier Fly, Wild and Domesticated Populations, Life History Traits, Maggot Production, Animal Feed

References
[1] Woodley NE (2011). A world catalog of the Stratiomyidae (Insecta: Diptera): A supplement with revisionary notes and errata. Myia, 12, 379–415.
[2] Leclercq, M. (1997). À propos de Hermetia illucens (Linnaeus, 1758) (“soldier fly”) (Diptera: Stratiomyidae: Hermetiinae). Bulletin et Annales de la Societé Royale belge d’Entomologie, 133,‎ 275-282.
[3] Cheng, J, Y., Chiu, S. L., & Lo, I, M. (2017). Effects of moisture content of food waste on residue separation, larval growth and larval survival in black soldier fly bioconversion. Waste Manage, 67, 315323. https://doi.org/10.1016/j.wasman.2017.05.046.
[4] Jucker, C, E, D., Leonardi, M, G., Lupi, D., & Savoldelli, S. (2017). Assessment of Vegetable and Fruit Substrates as Potential Rearing Media for Hermetia illucens (Diptera: Stratiomyidae) Larvae. Environmental Entomology, 46, 1415–1423.
[5] Nana, P., Kimpara, J, M., Tiambo, K, C., Tiogue, T, C., Youmbi, J., Choundong, B., & Fonkou, T. (2018). Black soldier flies (Hermetia illucens Linnaeus) as recyclers of organic waste and possible livestock feed. International Journal of Biological and Chemical Sciences, 12, 2004-2015.
[6] Dzepe, D., Nana, P., Kuietche, H, M., Kimpara, J, M., Magatsing, O., Tchuinkam, T., & Djouaka, R. (2021). Feeding strategies for small-scale rearing black soldier fly larvae (Hermetia illucens) as organic waste recycler. SN Applied Sciences, 3, 252. https://doi.org/10.1007/s42452-020-04039-5.
[7] Putra, E, K., Hutami, R., Suantika, G., & Rosmiati, M. (2017). Application of compost produced by bioconversion of coffee husk by black soldier fly larvae (Hermetia illucens) as solid fertilizer to lettuce (Lactuca sativa var. crispa): Impact to harvested biomass and utilization of nitrogen, phosphor, and potassium. Proceedings of the International Conference on Green Technolnology, 8, 20-26.
[8] Bruno, D., Bonelli, M., De Filippis, F., Di, Lelio I. et al (2019). The intestinal microbiota of Hermetia illucens larvae is affected by diet and shows a diverse composition in the different midgut regions. Applied and Environmental Microbiology, 85, 1-14. https://doi.org/10.1128/AEM.01864-18.
[9] Sarpong, D., Oduro-Kwarteng, S., Gyasi, S, F., Buamah, R. et al (2019). Biodegradation by composting of municipal organic solid waste into organic fertilizer using the black soldier fly (Hermetia illucens) (Diptera: Stratiomyidae) larvae. International Jouranl of Reclycling of Organic Waste in Agriculture, 8, 45–54. https://doi.org/10.1007/s40093-019-0268-4.
[10] Kawasaki, K., Kawasaki, T., Hirayasu, H., Matsumoto, Y., & Fujitani, Y. (2020). Evaluation of fertilizer value of residues obtained after processing household organic waste with black soldier fly (Hermetia illucens). Sustainability, 12, 4920. https://doi:10.3390/su12124920.
[11] Oonincx, D, G., Van Broekhoven, S., Van Huis, A., & Van Loon, J, J. (2015). Feed conversion, survival and development, and composition of four insect species on diets composed of food by-products. PLoS One, 10 (12), https://doi e0144601.
[12] Giannetto, A., Oliva, S., Ceccon Lanes, C, F., de Araújo Pedron, F., Savastano, D., Baviera, C., et al (2020). Hermetia illucens (Diptera: Stratiomydae) larvae and prepupae: biomass production, fatty acid profile and expression of key genes involved in lipid metabolism. Journal of Biotechnology, 307, 44–54. https://doi:10.1016/j.jbiotec. 2019.10.015.
[13] Maurer, V., Holinger, M., Amsler, Z., Früh, B., Wohlfahrt, J., Stamer, A., & Leiber, F. (2016). Replacement of soybean cake by Hermetia illucens meal in diets for layers. Journal of Insects as Food and Feed, 2, 83–90. https://doi.org/10.3920/JIFF2015.0071
[14] Schiavone, A., Cullere, M., De Marco, M., Meneguz, M., Biasato, I., Bergagna, S., Dezzutto, D., Gai, F., Dabbou, S. et al (2017). Partial or total replacement of soybean oil by black soldier fly larvae (Hermetia illucens L.) fat in broiler diets: effect on growth performances, feed choice, blood traits, carcass characteristics and meat quality. Italian Journal of Animal Science, 16, 93–100. https://doi/10.1080/1828051X.2016.1249968.
[15] Newton, G, L., Sheppard, D, C., Watson, D, W., Burtle, G, J., Dove, C, R., Tomberlin, J, K., & Thelen, E, E., (2005). The black soldier fly, Hermetia illucens, as a manure management/resource recovery tool. Symposium on the state of the science of Animal Manure and Waste Management, San Antonio.
[16] Bondari, K., & Sheppard, D, C. (1981). Soldier fly larvae as feed in commercial fish production. Aquaculture Research, 24, 103–109.
[17] St-Hilaire, S., Cranfill, K., McGuire, M, A., Mosley, E, E., Tomberlin, J, K., Newton, L., Sealey, W., Sheppard, C., & Irvin, S. (2007). Fish ofal recycling by the black soldier fly produces a foodstuff high in Omega-3 fatty acids. Journal of the World Aquaculture Society, 38, 309-313. https://doi.org/10.1111/j.1749-7345.2007.00101.X.
[18] Yu, G., Cheng, P., Chen, Y., Li, Y., Yang, Z., Chen, Y. et al (2011). Inoculating poultry manure with companion bacteria influences growth and development of black soldier fly (Diptera: Stratiomyidae) larvae. Environmental Entomology, 40, 30–35.https://doi: 10.1603/en10126.
[19] Lalander, C, H., Fidjeland, J., Diener, S., Eriksson, S., & Vinnerås, B. (2014). High waste-to-biomass conversion and efficient Salmonella spp. reduction using black soldier fly for waste recycling. Agronomy for Sustainaible Development, 35, 261–271.
[20] Boccazzi, I, V., Ottoboni, M., Martin, E., Comandatore, F., Vallone, L., Spranghers, T. et al. (2017). A survey of the mycobiota associated with larvae of the black soldier fly (Hermetia illucens) reared for feed production. PLoS One 12: e0182533. https://doi: 10.1371/journal.pone.0182533.
[21] Tomberlin, J, K., Adler, P., & Myers, H, M. (2009). ‘Development of the Black Soldier Fly (Diptera: Stratiomyidae) in Relation to Temperature: Table 1.’ Environmental Entomology, 38, 930–934. https://doi: 10.1603/022.038.0347.
[22] Tomberlin, J, K., Sheppard, D, C., & Joyce, J, A. (2002). Selected life-history traits of black soldier flies (Diptera: Stratiomyidae) reared on three artificial diets. Entomological Socociety of America, 95, 379–386. https://doi.org/10.1603/00138746(2002)095[0379:SLHTOB]2.0.CO;2.
[23] Nakamura, S., Ichiki, R, T., Shimoda, M., & Morioka, S. (2016). Small-scale rearing of the black soldier fly, Hermetia illucens (Diptera: Stratiomyidae), in the laboratory: low-cost and year-round rearing. Applied Entomology and Zoology, 51, 161–166. https://doi.org/10.1007/s13355-015-0376-1.
[24] Julita, U., Fitri, L, L., Putra, R, E., & Permana, A, D. (2020). Mating success and reproductive behavior of black soldier fly Hermetia illucens L. (Diptera, Stratiomyidae) in Tropics. Journal of Entomology, 17, 117-127.
[25] Oliveira, F, R., Doelle, K., & Smith, R, P. (2016). External Morphology of Hermetia illucens Stratiomyidae: Diptera (L. 1758) Based on Electron Microscopy. Annual Research and Review in Biology, 9, 1-10.
[26] Barros, L. M., Gutjahr, A, L, N., Ferreira Keppler, R, L., & Martins, R, T. (2019). Morphological description of the immature stages of Hermetia illucens (Linnaeus, 1758) (Diptera: Stratiomyidae). Microsccopy Research and Technique, 82, 178–189. https://doi.org/10.1002/jemt.23127.
[27] Olivry, J, C. (1986). Fleuves et rivières du Cameroun. Office de la recherche scientifique et technique d’outre-mer. Collection «Monographies Hydroliques ORSTOM». Série 9, 1–78.
[28] Mbansie, G, L., Ngo Libong, S, G., Mamno Totuom, C, S., Taya Saah, B, J., Makon, S, D., & Mbenoun Masse, P, S. (2022). Effets de l’alimentation sur les performances de croissance et le sex-ratio de la mouche soldat noire Hermetia illucens (Diptera: Stratiomyidae). International Journal of Biological and Chemical Sciences, 16, 772-786.
[29] Kim, J, G., Choi, Y, C., Choi, J, Y., Kim, W, T., Jeong, G, S., Park, K, H., & Hwang, S, J. (2008). Ecology of the black soldier fly, Hermetia illucens (Diptera; Stratiomyidae) in Korea. Korean Journal of Applied Entomology, 47, 337–343.
[30] Holmes, L, A., Vanlaerhoven, S, L., & Tomberlin, J, K. (2013). Substrate effects on pupation and adult emergence of Hermetia illucens (Diptera: Stratiomyidae). Environmental Entomology, 42, 370-374.
[31] Dzepe, D., Nana, P., Mube, K, H., Fotso, K, A., Tchuinkam, T., & Djouaka, R. (2020). Role of pupation substrate on post-feeding development of black soldier fy larvae, Hermetia illucens (Diptera: stratiomyidae). Jouranl of Entomology and Zoological Studies, 8, 760–764.
[32] Booth, D, C., & Sheppard, C. (1984). Oviposition of the black soldier fly, Hermetia illucens (Diptera, Stratiomyidae): eggs, masses, timing and site characteristics. Journal of Environmental Entomology, 13, 421-423. https://doi.org/10.1093/ee/13.2.421.
[33] James, M. T. (1935). The genus Hermetia in the United States (Diptera: Stratiomyidae). Bulletin of the Brooklyn Entomology Society, 30, 165-170.
[34] Robacker, D, C., Moreno, D, S., & Demilo, A, B. (1996). Attractiveness to Mexican fruit flies of combinations of acetic acid with ammonium/ amino attractants with emphasis on effects of hunger. Journal of Chemical Ecology, 22, 499-511.
[35] Darwin, C. (1868). The Variation of Animals and Plants Under Domestication. John Murray, Albermarle Street.
[36] Hammer, K. (1984). Das Domestikation syndrom. Kulturpflanze, 32, 11–34.
[37] Driscoll, C. A., Macdonald, D. W., & O’Brien, S, J. (2009). From wild animals to domestic pets, an evolutionary view of domestication. Proceedings of the National Academy of Sciences USA, 106, 9971–9978. https://doi.org/10.1073/pnas.0901586106.
[38] Trut, L., Oskina, I. & Kharlamova, A. (2009). Animal evolution during domestication: the domesticated fox as a model. BioEssays, 31, 349–360. https://doi.org/10.1002/bies.200800070.
[39] Wilkins, A, S., Wrangham, R, W., & Fitch, W, T. (2014). The ‘domestication syndrome’ in mammals: a unified explanation based on neural crest cell behavior and genetics. Genetics, 197, 795–808. https://doi.org/10.1534/genetics.114.165423.
[40] Zeller, U., & Gottert, T. (2019). The relations between evolution and domestication reconsidered-implications for systematics, ecology, and nature conservation. Global Ecology and Conservation, 20. https://doi:e00456.
[41] Meyer, R, S., DuVal, A, E., & Jensen, H, R. (2012). Patterns and Processes in Crop Domestication: An Historical Review and Quantitative Analysis of 203 Global Food Crops: Tansley Review. New Phytologist, 196, 29–48. https://doi.org//10.1111/j.1469-8137.2012.04253.x.
[42] Templeton, A, R. (1981). Mechanisms of speciation, a population genetic approach. Annual Review of Ecology and Systematics, 12, 23-48. doi: 10.1146/annurev.es.12.110181.000323.
[43] UN (2019). Word population prospects, population data, file: Population growth rate, median variant tab.
[44] FAO (2021). New interactive report shows africa’s growing hunger crisis. www.fao.org/detail/en. Accessed on 14/12/2021.
Cite This Article
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    Mbenoun Masse Paul Serge, Mbansie Gbetkom Loudh, Yede, Ngo Libong Sipora Glwadys, Mamno Totuom Clarette Sidoine, et al. (2023). Differences in Life History Traits and Morphology in Wild vs. Domesticated Populations of Black Soldier Fly, Hermetia illucens (Diptera: Stratiomyidae). Animal and Veterinary Sciences, 11(3), 71-79. https://doi.org/10.11648/j.avs.20231103.13

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    ACS Style

    Mbenoun Masse Paul Serge; Mbansie Gbetkom Loudh; Yede; Ngo Libong Sipora Glwadys; Mamno Totuom Clarette Sidoine, et al. Differences in Life History Traits and Morphology in Wild vs. Domesticated Populations of Black Soldier Fly, Hermetia illucens (Diptera: Stratiomyidae). Anim. Vet. Sci. 2023, 11(3), 71-79. doi: 10.11648/j.avs.20231103.13

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    AMA Style

    Mbenoun Masse Paul Serge, Mbansie Gbetkom Loudh, Yede, Ngo Libong Sipora Glwadys, Mamno Totuom Clarette Sidoine, et al. Differences in Life History Traits and Morphology in Wild vs. Domesticated Populations of Black Soldier Fly, Hermetia illucens (Diptera: Stratiomyidae). Anim Vet Sci. 2023;11(3):71-79. doi: 10.11648/j.avs.20231103.13

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  • @article{10.11648/j.avs.20231103.13,
      author = {Mbenoun Masse Paul Serge and Mbansie Gbetkom Loudh and Yede and Ngo Libong Sipora Glwadys and Mamno Totuom Clarette Sidoine and Bilong Bilong Charles Felix},
      title = {Differences in Life History Traits and Morphology in Wild vs. Domesticated Populations of Black Soldier Fly, Hermetia illucens (Diptera: Stratiomyidae)},
      journal = {Animal and Veterinary Sciences},
      volume = {11},
      number = {3},
      pages = {71-79},
      doi = {10.11648/j.avs.20231103.13},
      url = {https://doi.org/10.11648/j.avs.20231103.13},
      eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.avs.20231103.13},
      abstract = {The Black Soldier Fly (BSF) Hermetia illucens is widely studied as a sustainable alternative source of protein. Herein, we evaluated the changes in life history and morphometric traits between wild (WP) and domesticated populations (DP) with implications for larval biomass production. Prepupa stages of both populations were maintained under the same rearing conditions from July 2020 to June 2021. Our results show that the pupation time was longer in WP (10.25 ± 2.66 days) than in DP (7.2 ± 1.1 days). In contrast, the emergence time of BSF adults was shorter in WP (8.3 ± 2.2 days) than in DP (9.7 ± 1.8 days). The courtship was nearly similar in both populations. Mounting and reverse coupling were the two different copulation models used by BSF adults in WP while reverse coupling dominated in DP. The BSF females laid more eggs in WP (1468.75 ± 593.09 eggs) than in DP (246.21 ± 96.23 eggs). The egg stage was similar in length and width in both populations while the morphometric traits in the larval, pupal and adult stages were consistently lower in domesticated than in wild population. The life span of adults (males and females) was longer in DP than in WP. Our findings indicate higher values of morphological traits in WP than in DP, and distinct mating and reproductive behaviours between both populations. Our results suggest ‘domestication syndrome hypothesis’ as the main cause of changes in reproductive behaviour and reduction of size in DP. Therefore, wild population of H. illucens seems be more suitable for maggot mass production as an alternative source of protein for animal feed production.},
     year = {2023}
    }
    

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  • TY  - JOUR
    T1  - Differences in Life History Traits and Morphology in Wild vs. Domesticated Populations of Black Soldier Fly, Hermetia illucens (Diptera: Stratiomyidae)
    AU  - Mbenoun Masse Paul Serge
    AU  - Mbansie Gbetkom Loudh
    AU  - Yede
    AU  - Ngo Libong Sipora Glwadys
    AU  - Mamno Totuom Clarette Sidoine
    AU  - Bilong Bilong Charles Felix
    Y1  - 2023/06/06
    PY  - 2023
    N1  - https://doi.org/10.11648/j.avs.20231103.13
    DO  - 10.11648/j.avs.20231103.13
    T2  - Animal and Veterinary Sciences
    JF  - Animal and Veterinary Sciences
    JO  - Animal and Veterinary Sciences
    SP  - 71
    EP  - 79
    PB  - Science Publishing Group
    SN  - 2328-5850
    UR  - https://doi.org/10.11648/j.avs.20231103.13
    AB  - The Black Soldier Fly (BSF) Hermetia illucens is widely studied as a sustainable alternative source of protein. Herein, we evaluated the changes in life history and morphometric traits between wild (WP) and domesticated populations (DP) with implications for larval biomass production. Prepupa stages of both populations were maintained under the same rearing conditions from July 2020 to June 2021. Our results show that the pupation time was longer in WP (10.25 ± 2.66 days) than in DP (7.2 ± 1.1 days). In contrast, the emergence time of BSF adults was shorter in WP (8.3 ± 2.2 days) than in DP (9.7 ± 1.8 days). The courtship was nearly similar in both populations. Mounting and reverse coupling were the two different copulation models used by BSF adults in WP while reverse coupling dominated in DP. The BSF females laid more eggs in WP (1468.75 ± 593.09 eggs) than in DP (246.21 ± 96.23 eggs). The egg stage was similar in length and width in both populations while the morphometric traits in the larval, pupal and adult stages were consistently lower in domesticated than in wild population. The life span of adults (males and females) was longer in DP than in WP. Our findings indicate higher values of morphological traits in WP than in DP, and distinct mating and reproductive behaviours between both populations. Our results suggest ‘domestication syndrome hypothesis’ as the main cause of changes in reproductive behaviour and reduction of size in DP. Therefore, wild population of H. illucens seems be more suitable for maggot mass production as an alternative source of protein for animal feed production.
    VL  - 11
    IS  - 3
    ER  - 

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Author Information
  • Laboratory of Zoology, University of Yaoundé 1, Yaoundé, Cameroun

  • Laboratory of Zoology, University of Yaoundé 1, Yaoundé, Cameroun

  • Laboratory of Zoology, University of Yaoundé 1, Yaoundé, Cameroun

  • Laboratory of Hydrobiology and Environment, University of Yaoundé 1, Yaoundé, Cameroun

  • Laboratory of Biochemistry, University of Yaoundé 1, Yaoundé, Cameroun

  • Laboratory of Parasitology and Ecology, University of Yaoundé 1, Yaoundé, Cameroun

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