Worming the Circular Economy for Biowaste and Plastics: Hermetia illucens, Tenebrio molitor, and Zophobas morio
Abstract
:1. Introduction
2. Factors Affecting the Growth of Hermetia illucens
3. Hermetia illucens in Organic Waste Treatment
3.1. Challenges in Implementation of Hermetia illucens Biowaste Treatment
3.2. Potential Dangers in Biowaste Processing of Hermetia illucens Larvae
3.3. Hermetia illucens as a Feed for Livestock
4. Hermetia illucens in the Management of Carcasses and Corpses
5. Zophobas morio and Tenebrio molitor in the Plastic Waste Circular Economy
5.1. Polyethylene (PE)
5.1.1. Biodegradation Rate of PE by Tenebrio molitor
5.1.2. Biodegradation Rate of PE by Zophobas morio
5.2. Polystyrene (PS)
5.2.1. Biodegradation Rate of PS by Tenebrio molitor
5.2.2. Biodegradation Rate of PS by Zophobas morio
5.3. Challenges in Plastic Waste Treatment by Larvae
- Prolonged incubation with the worms, given that PS/PE degradation by these worms is slow [49], though still millions of times faster than natural degradation of plastic. The advantage is that the worms require little maintenance, can eat food-contaminated plastics, and do not fly, doing away with cleaning and making containment easier to implement.
- Multiple layers of worm feeding chambers to decrease the microplastic content. Lower levels of worms consume the frass to reduce undigested plastics, microplastics, and monomer content [34].
- Depolymerisation of the PS/PE waste into smaller fragments such as dimers, trimers, etc., to decrease the density for easier consumption by the worms.
6. Insects as a Source of Feed for Monogastric Animals
6.1. Constitution and Potential of Hermetia illucens Larvae in the Market
6.2. Tenebrio molitor as an Alternative Source of Protein
6.3. Zophobas morio as an Alternative Source of Protein
6.4. Concerns about Larvae as Feed
7. Entomophagy by Humans
8. Conclusions
Author Contributions
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Acknowledgments
Conflicts of Interest
References
- Statista Market Forecast. Platform-to-Consumer Delivery—Worldwide. Available online: https://www.statista.com/outlook/dmo/eservices/online-food-delivery/platform-to-consumer-delivery/worldwide (accessed on 9 October 2021).
- Dhir, A.; Talwar, S.; Kaur, P.; Malibari, A. Food Waste in Hospitality and Food Services: A Systematic Literature Review and Framework Development Approach. J. Clean. Prod. 2020, 270, 122861. [Google Scholar] [CrossRef]
- United Nations Department of Economic and Social Affairs. Goal 12 Ensure Sustainable Consumption and Production Patterns. Available online: https://sdgs.un.org/goals/goal12 (accessed on 9 October 2021).
- ThinkEatSave. Worldwide Food Waste. Available online: https://www.unep.org/thinkeatsave/get-informed/worldwide-food-waste (accessed on 30 September 2021).
- Schweitzer, J.-P.; Gionfra, S.; Pantzar, M.; Mottershead, D.; Watkins, E.; Petsinaris, F. Unwrapped: How Throwaway Plastic Is Failing to Solve Europe’s Food Waste Problem (and What We Need to Do Instead); Institute for European Environmental Policy AISBL: Brussels, Belgium, 2018; p. 28. [Google Scholar]
- Global Plastic Production 1950–2020. Available online: https://www.statista.com/statistics/282732/global-production-of-plastics-since-1950/ (accessed on 17 October 2021).
- Measuring Biodegradability. Available online: https://www.sciencelearn.org.nz/resources/1543-measuring-biodegradability (accessed on 30 September 2021).
- WWF. Fight Climate Change by Preventing Food Waste. Available online: https://www.worldwildlife.org/stories/fight-climate-change-by-preventing-food-waste (accessed on 30 September 2021).
- Čičková, H.; Newton, G.L.; Lacy, R.C.; Kozánek, M. The Use of Fly Larvae for Organic Waste Treatment. Waste Manag. 2015, 35, 68–80. [Google Scholar] [CrossRef] [PubMed]
- Nguyen, T.T.X.; Tomberlin, J.K.; Vanlaerhoven, S. Ability of Black Soldier Fly (Diptera: Stratiomyidae) Larvae to Recycle Food Waste. Environ. Entomol. 2015, 44, 406–410. [Google Scholar] [CrossRef] [PubMed]
- Singh, A.; Kumari, K. An Inclusive Approach for Organic Waste Treatment and Valorisation Using Black Soldier Fly Larvae: A Review. J. Environ. Manag. 2019, 251, 109569. [Google Scholar] [CrossRef] [PubMed]
- Raksasat, R.; Lim, J.W.; Kiatkittipong, W.; Kiatkittipong, K.; Ho, Y.C.; Lam, M.K.; Font-Palma, C.; Mohd Zaid, H.F.; Cheng, C.K. A Review of Organic Waste Enrichment for Inducing Palatability of Black Soldier Fly Larvae: Wastes to Valuable Resources. Environ. Pollut. 2020, 267, 115488. [Google Scholar] [CrossRef] [PubMed]
- Ritchie, H.; Roser, M. Plastic Pollution. Our World Data 2018. Available online: https://ourworldindata.org/plastic-pollution?utm_source=newsletter (accessed on 30 September 2021).
- Yang, Y.; Wang, J.; Xia, M. Biodegradation and Mineralization of Polystyrene by Plastic-Eating Superworms Zophobas Atratus. Sci. Total Environ. 2020, 708, 135233. [Google Scholar] [CrossRef] [PubMed]
- Diclaro, J.W., II; Kaufman, P.E. Black Soldier Fly—Hermetia illucens. Available online: https://entnemdept.ufl.edu/creatures/livestock/black_soldier_fly.htm (accessed on 30 September 2021).
- Barragan-Fonseca, K.B.; Dicke, M.; van Loon, J.J.A. Influence of Larval Density and Dietary Nutrient Concentration on Performance, Body Protein, and Fat Contents of Black Soldier Fly Larvae (Hermetia illucens). Entomol. Exp. Appl. 2018, 166, 761–770. [Google Scholar] [CrossRef] [Green Version]
- Sheppard, D.C.; Newton, G.L.; Thompson, S.A.; Savage, S. A Value Added Manure Management System Using the Black Soldier Fly. Bioresour. Technol. 1994, 50, 275–279. [Google Scholar] [CrossRef]
- Miranda, C.D.; Cammack, J.A.; Tomberlin, J.K. Mass Production of the Black Soldier Fly, Hermetia illucens (L.), (Diptera: Stratiomyidae) Reared on Three Manure Types. Animals 2020, 10, 1243. [Google Scholar] [CrossRef]
- Effects of the Artificial Diet with Low Water Content on the Growth and Development of the Black Soldier Fly, Hermetia illucens (Diptera: Stratiomyidae). Available online: https://www.cabdirect.org/cabdirect/abstract/20143395658 (accessed on 17 October 2021).
- Chia, S.Y.; Tanga, C.M.; Khamis, F.M.; Mohamed, S.A.; Salifu, D.; Sevgan, S.; Fiaboe, K.K.M.; Niassy, S.; van Loon, J.J.A.; Dicke, M.; et al. Threshold Temperatures and Thermal Requirements of Black Soldier Fly Hermetia illucens: Implications for Mass Production. PLoS ONE 2018, 13, e0206097. [Google Scholar] [CrossRef] [Green Version]
- Zhou, F.; Tomberlin, J.K.; Zheng, L.; Yu, Z.; Zhang, J. Developmental and Waste Reduction Plasticity of Three Black Soldier Fly Strains (Diptera: Stratiomyidae) Raised on Different Livestock Manures. J. Med. Entomol. 2013, 50, 1224–1230. [Google Scholar] [CrossRef] [PubMed]
- Mazza, L.; Xiao, X.; ur Rehman, K.; Cai, M.; Zhang, D.; Fasulo, S.; Tomberlin, J.K.; Zheng, L.; Soomro, A.A.; Yu, Z.; et al. Management of Chicken Manure Using Black Soldier Fly (Diptera: Stratiomyidae) Larvae Assisted by Companion Bacteria. Waste Manag. 2020, 102, 312–318. [Google Scholar] [CrossRef] [PubMed]
- feednavigator.com. Study Shows Efficiency of BSF and Bacteria for Producing Larvae as Feedstuff and Fertilizer. Available online: https://www.feednavigator.com/Article/2018/09/06/Study-shows-efficiency-of-BSF-and-bacteria-for-producing-larvae-as-feedstuff-and-fertilizer (accessed on 30 September 2021).
- Parodi, A.; Van Dijk, K.; Van Loon, J.J.A.; Van Boer, I.J.M.; Van Schelt, J.; Van Zanten, H.H.E. Black Soldier Fly Larvae Show a Stronger Preference for Manure than for a Mass-rearing Diet. J. Appl. Entomol. 2020, 144, 560–565. [Google Scholar] [CrossRef]
- Zurbrügg, C.; Dortmans, B.; Fadhila, A.; Verstappen, B.; Diener, S. From Pilot to Full Scale Operation of a Waste-to-Protein Treatment Facility. Detritus 2018, 1, 18–22. [Google Scholar] [CrossRef]
- Gold, M.; Tomberlin, J.K.; Diener, S.; Zurbrügg, C.; Mathys, A. Decomposition of Biowaste Macronutrients, Microbes, and Chemicals in Black Soldier Fly Larval Treatment: A Review. Waste Manag. 2018, 82, 302–318. [Google Scholar] [CrossRef]
- Manzano-Agugliaro, F.; Sanchez-Muros, M.J.; Barroso, F.G.; Martínez-Sánchez, A.; Rojo, S.; Pérez-Bañón, C. Insects for Biodiesel Production. Renew. Sustain. Energy Rev. 2012, 16, 3744–3753. [Google Scholar] [CrossRef]
- Nkukwana, T.T. Global Poultry Production: Current Impact and Future Outlook on the South African Poultry Industry. S. Afr. J. Anim. Sci. 2018, 48, 869–884. [Google Scholar] [CrossRef]
- Joosten, L.; Lecocq, A.; Jensen, A.B.; Haenen, O.; Schmitt, E.; Eilenberg, J. Review of Insect Pathogen Risks for the Black Soldier Fly (Hermetia illucens) and Guidelines for Reliable Production. Entomol. Exp. Appl. 2020, 168, 432–447. [Google Scholar] [CrossRef]
- De Marco, M.; Martínez, S.; Hernandez, F.; Madrid, J.; Gai, F.; Rotolo, L.; Belforti, M.; Bergero, D.; Katz, H.; Dabbou, S.; et al. Nutritional Value of Two Insect Larval Meals (Tenebrio molitor and Hermetia illucens) for Broiler Chickens: Apparent Nutrient Digestibility, Apparent Ileal Amino Acid Digestibility and Apparent Metabolizable Energy. Anim. Feed Sci. Technol. 2015, 209, 211–218. [Google Scholar] [CrossRef]
- Pujol-Luz, J.; da Costa Francez, P.A.; Ururahy-Rodrigues, A.; Constantino, R. The Black Soldier-Fly, Hermetia illucens (Diptera, Stratiomyidae), Used to Estimate the Postmortem Interval in a Case in Amapá State, Brazil. J. Forensic Sci. 2008, 53, 476–478. [Google Scholar] [CrossRef]
- Barros, L.M.; Ferreira-Keppler, R.L.; Martins, R.T.; Gutjahr, A.L.N. Bionomy of Hermetia illucens (Diptera: Stratiomyidae) on Decomposing Swine Carcass in an Urban Area of Central Amazon. J. Med. Entomol. 2019, 56, 681–689. [Google Scholar] [CrossRef] [PubMed]
- Lee, H.M.; Kim, H.R.; Jeon, E.; Yu, H.C.; Lee, S.; Li, J.; Kim, D.-H. Evaluation of the Biodegradation Efficiency of Four Various Types of Plastics by Pseudomonas Aeruginosa Isolated from the Gut Extract of Superworms. Microorganisms 2020, 8, 1341. [Google Scholar] [CrossRef] [PubMed]
- Gan, S.K.-E.; Phua, S.-X.; Yeo, J.Y.; Heng, Z.S.-L.; Xing, Z. Method for Zero-Waste Circular Economy Using Worms for Plastic Agriculture: Augmenting Polystyrene Consumption and Plant Growth. Methods Protoc. 2021, 4, 43. [Google Scholar] [CrossRef] [PubMed]
- Yang, S.-S.; Brandon, A.M.; Andrew Flanagan, J.C.; Yang, J.; Ning, D.; Cai, S.-Y.; Fan, H.-Q.; Wang, Z.-Y.; Ren, J.; Benbow, E.; et al. Biodegradation of Polystyrene Wastes in Yellow Mealworms (Larvae of Tenebrio molitor Linnaeus): Factors Affecting Biodegradation Rates and the Ability of Polystyrene-Fed Larvae to Complete Their Life Cycle. Chemosphere 2018, 191, 979–989. [Google Scholar] [CrossRef]
- Peng, B.-Y.; Su, Y.; Chen, Z.; Chen, J.; Zhou, X.; Benbow, M.E.; Criddle, C.S.; Wu, W.-M.; Zhang, Y. Biodegradation of Polystyrene by Dark (Tenebrio Obscurus) and Yellow (Tenebrio molitor) Mealworms (Coleoptera: Tenebrionidae). Environ. Sci. Technol. 2019, 53, 5256–5265. [Google Scholar] [CrossRef]
- Kim, H.R.; Lee, H.M.; Yu, H.C.; Jeon, E.; Lee, S.; Li, J.; Kim, D.-H. Biodegradation of Polystyrene by Pseudomonas Sp. Isolated from the Gut of Superworms (Larvae of Zophobas Atratus). Environ. Sci. Technol. 2020, 54, 6987–6996. [Google Scholar] [CrossRef]
- LeMoine, C.M.R.; Grove, H.C.; Smith, C.M.; Cassone, B.J. A Very Hungry Caterpillar: Polyethylene Metabolism and Lipid Homeostasis in Larvae of the Greater Wax Moth (Galleria Mellonella). Environ. Sci. Technol. 2020, 54, 14706–14715. [Google Scholar] [CrossRef]
- This Bug Can Eat Plastic. But Can It Clean Up Our Mess? Available online: https://www.nationalgeographic.com/science/article/wax-worms-eat-plastic-polyethylene-trash-pollution-cleanup (accessed on 25 October 2021).
- Chamas, A.; Moon, H.; Zheng, J.; Qiu, Y.; Tabassum, T.; Jang, J.H.; Abu-Omar, M.; Scott, S.L.; Suh, S. Degradation Rates of Plastics in the Environment. ACS Sustain. Chem. Eng. 2020, 8, 3494–3511. [Google Scholar] [CrossRef] [Green Version]
- Wu, W.; Yang, S.; Brandon, A.M.; Yang, Y.; Flanagan, J.A.; Fan, H.Q.; Cai, S.Y.; Wang, Z.Y.; Din, L.Y.; Daliang, N.; et al. Rapid Biodegradation of Plastics by Mealworms (Larvae of Tenebrio molitor) Brings Hope to Solve Wasteplastic Pollution. In Proceedings of the AGU Fall Meeting 2016, San Francisco, CA, USA, 12–16 December 2016. [Google Scholar]
- Wu, Q.; Tao, H.; Wong, M.H. Feeding and Metabolism Effects of Three Common Microplastics on Tenebrio molitor L. Environ. Geochem. Health 2019, 41, 17–26. [Google Scholar] [CrossRef]
- Yang, S.-S.; Wu, W.-M.; Brandon, A.M.; Fan, H.-Q.; Receveur, J.P.; Li, Y.; Wang, Z.-Y.; Fan, R.; McClellan, R.L.; Gao, S.-H.; et al. Ubiquity of Polystyrene Digestion and Biodegradation within Yellow Mealworms, Larvae of Tenebrio molitor Linnaeus (Coleoptera: Tenebrionidae). Chemosphere 2018, 212, 262–271. [Google Scholar] [CrossRef] [Green Version]
- Yang, S.-S.; Ding, M.-Q.; Zhang, Z.-R.; Ding, J.; Bai, S.-W.; Cao, G.-L.; Zhao, L.; Pang, J.-W.; Xing, D.-F.; Ren, N.-Q.; et al. Confirmation of Biodegradation of Low-Density Polyethylene in Dark- versus Yellow- Mealworms (Larvae of Tenebrio Obscurus versus Tenebrio molitor) via. Gut Microbe-Independent Depolymerization. Sci. Total Environ. 2021, 789, 147915. [Google Scholar] [CrossRef]
- Peng, B.-Y.; Li, Y.; Fan, R.; Chen, Z.; Chen, J.; Brandon, A.M.; Criddle, C.S.; Zhang, Y.; Wu, W.-M. Biodegradation of Low-Density Polyethylene and Polystyrene in Superworms, Larvae of Zophobas Atratus (Coleoptera: Tenebrionidae): Broad and Limited Extent Depolymerization. Environ. Pollut. 2020, 266, 115206. [Google Scholar] [CrossRef] [PubMed]
- Yang, S.S.; Brandon, A.M.; Xing, D.F.; Yang, J.; Pang, J.W.; Criddle, C.S.; Ren, N.Q.; Wu, W.M. Progresses in Polystyrene Biodegradation and Prospects for Solutions to Plastic Waste Pollution. IOP Conf. Ser. Earth Environ. Sci. 2018, 150, 012005. [Google Scholar] [CrossRef] [Green Version]
- Yang, L.; Gao, J.; Liu, Y.; Zhuang, G.; Peng, X.; Wu, W.-M.; Zhuang, X. Biodegradation of Expanded Polystyrene and Low-Density Polyethylene Foams in Larvae of Tenebrio molitor Linnaeus (Coleoptera: Tenebrionidae): Broad versus Limited Extent Depolymerization and Microbe-Dependence versus Independence. Chemosphere 2021, 262, 127818. [Google Scholar] [CrossRef] [PubMed]
- Scott-Clarke, E.; Page, T. Can Plastic-Eating Mealworms Help Solve Our Pollution Crisis? Available online: https://www.cnn.com/2020/09/10/world/mealworms-bacteria-plastic-waste-c2e-spc-intl/index.html (accessed on 30 September 2021).
- Yang, Y.; Yang, J.; Wu, W.-M.; Zhao, J.; Song, Y.; Gao, L.; Yang, R.; Jiang, L. Biodegradation and Mineralization of Polystyrene by Plastic-Eating Mealworms: Part 1. Chemical and Physical Characterization and Isotopic Tests. Environ. Sci. Technol. 2015, 49, 12080–12086. [Google Scholar] [CrossRef] [PubMed]
- Yang, Y.; Yang, J.; Wu, W.-M.; Zhao, J.; Song, Y.; Gao, L.; Yang, R.; Jiang, L. Biodegradation and Mineralization of Polystyrene by Plastic-Eating Mealworms: Part 2. Role of Gut Microorganisms. Environ. Sci. Technol. 2015, 49, 12087–12093. [Google Scholar] [CrossRef] [PubMed]
- Approval of First Insect as Novel Food. Available online: https://ec.europa.eu/food/safety/novel-food/authorisations/approval-first-insect-novel-food_en (accessed on 30 September 2021).
- Schiavone, A.; De Marco, M.; Martínez, S.; Dabbou, S.; Renna, M.; Madrid, J.; Hernandez, F.; Rotolo, L.; Costa, P.; Gai, F.; et al. Nutritional Value of a Partially Defatted and a Highly Defatted Black Soldier Fly Larvae (Hermetia illucens L.) Meal for Broiler Chickens: Apparent Nutrient Digestibility, Apparent Metabolizable Energy and Apparent Ileal Amino Acid Digestibility. J. Anim. Sci. Biotechnol. 2017, 8, 51. [Google Scholar] [CrossRef]
- Smetana, S.; Palanisamy, M.; Mathys, A.; Heinz, V. Sustainability of Insect Use for Feed and Food: Life Cycle Assessment Perspective. J. Clean. Prod. 2016, 137, 741–751. [Google Scholar] [CrossRef]
- Liu, X.; Chen, X.; Wang, H.; Yang, Q.; ur Rehman, K.; Li, W.; Cai, M.; Li, Q.; Mazza, L.; Zhang, J.; et al. Dynamic Changes of Nutrient Composition throughout the Entire Life Cycle of Black Soldier Fly. PLoS ONE 2017, 12, e0182601. [Google Scholar] [CrossRef] [Green Version]
- Oonincx, D.G.A.B.; van Broekhoven, S.; van Huis, A.; van Loon, J.J.A. Feed Conversion, Survival and Development, and Composition of Four Insect Species on Diets Composed of Food By-Products. PLoS ONE 2015, 10, e0144601. [Google Scholar] [CrossRef] [Green Version]
- Scriber, J.M.; Slansky, F., Jr. The Nutritional Ecology of Immature Insects. Annu. Rev. Entomol. 1981, 26, 183–211. [Google Scholar] [CrossRef]
- van Broekhoven, S.; Oonincx, D.G.A.B.; van Huis, A.; van Loon, J.J.A. Growth Performance and Feed Conversion Efficiency of Three Edible Mealworm Species (Coleoptera: Tenebrionidae) on Diets Composed of Organic by-Products. J. Insect Physiol. 2015, 73, 1–10. [Google Scholar] [CrossRef] [PubMed]
- Hong, J.; Han, T.; Kim, Y.Y. Mealworm (Tenebrio molitor Larvae) as an Alternative Protein Source for Monogastric Animal: A Review. Animals 2020, 10, 2068. [Google Scholar] [CrossRef] [PubMed]
- The Yellow Mealworm as a Novel Source of Protein. Available online: https://www.cabdirect.org/cabdirect/abstract/20103053822 (accessed on 30 September 2021).
- EFSA Says Mealworms Safe for Human Consumption: ‘An Important Milestone towards Commercialisation’. Available online: https://www.foodnavigator.com/Article/2021/01/14/EFSA-says-mealworms-safe-for-human-consumption-An-important-milestone-towards-commercialisation (accessed on 16 November 2021).
- Finke, M.D. The Use of Nonlinear Models to Evaluate the Nutritional Quality of Insect Protein (Logistic Model). Ph.D. Thesis, The University of Wisconsin, Madison, WI, USA, 1984. Available online: https://www.proquest.com/openview/77a510eb6e462d577628b6c8bd52e2ec/1?pq-origsite=gscholar&cbl=18750&diss=y (accessed on 30 September 2021).
- Barker, D.; Fitzpatrick, M.P.; Dierenfeld, E.S. Nutrient Composition of Selected Whole Invertebrates. Zoo Biol. 1998, 17, 123–134. [Google Scholar] [CrossRef]
- Poelaert, C.; Beckers, Y.; Despret, X.; Portetelle, D.; Francis, F.; Bindelle, J. In Vitro Evaluation of Fermentation Characteristics of Two Types of Insects as Potential Novel Protein Feeds for Pigs1. J. Anim. Sci. 2016, 94, 198–201. [Google Scholar] [CrossRef] [Green Version]
- Sedgh-Gooya, S.; Torki, M.; Darbemamieh, M.; Khamisabadi, H.; Torshizi, M.A.K.; Abdolmohamadi, A. Yellow Mealworm, Tenebrio molitor (Col: Tenebrionidae), Larvae Powder as Dietary Protein Sources for Broiler Chickens: Effects on Growth Performance, Carcass Traits, Selected Intestinal Microbiota and Blood Parameters. J. Anim. Physiol. Anim. Nutr. 2021, 105, 119–128. [Google Scholar] [CrossRef] [PubMed]
- Din, A.R.J.M.; Razak, S.A.; Sabaratnam, V. Nutritive Potential and Utilization of Super Worm (Zophobas morio) Meal in the Diet of Nile Tilapia (Oreochromis Niloticus) Juvenile. Afr. J. Biotechnol. 2012, 11, 6592–6598. [Google Scholar] [CrossRef] [Green Version]
- Rumbos, C.I.; Athanassiou, C.G. The Superworm, Zophobas morio (Coleoptera:Tenebrionidae): A ‘Sleeping Giant’ in Nutrient Sources. J. Insect Sci. 2021, 21, 13. [Google Scholar] [CrossRef]
- Van Huis, A. Insects as Food and Feed, a New Emerging Agricultural Sector: A Review. J. Insects Food Feed 2020, 6, 27–44. [Google Scholar] [CrossRef] [Green Version]
- Attygalle, A.B.; Blankespoor, C.L.; Meinwald, J.; Eisner, T. Defensive Secretion of Tenebrio molitor (Coleoptera: Tenebrionidae). J. Chem. Ecol. 1991, 17, 805–809. [Google Scholar] [CrossRef]
- Lis, L.; Bakula, T.; Baranowski, M.; Czarnewicz, A. The Carcinogenic Effects of Benzoquinones Produced by the Flour Beetle. Pol. J. Vet. Sci. 2011, 14, 159–164. [Google Scholar] [CrossRef] [Green Version]
- Yun, J.-H.; Roh, S.W.; Whon, T.W.; Jung, M.-J.; Kim, M.-S.; Park, D.-S.; Yoon, C.; Nam, Y.-D.; Kim, Y.-J.; Choi, J.-H.; et al. Insect Gut Bacterial Diversity Determined by Environmental Habitat, Diet, Developmental Stage, and Phylogeny of Host. Appl. Environ. Microbiol. 2014, 80, 5254–5264. [Google Scholar] [CrossRef] [Green Version]
- Dematheis, F.; Kurtz, B.; Vidal, S.; Smalla, K. Microbial Communities Associated with the Larval Gut and Eggs of the Western Corn Rootworm. PLoS ONE 2012, 7, e44685. [Google Scholar] [CrossRef]
- Douglas, A.E. Multiorganismal Insects: Diversity and Function of Resident Microorganisms. Annu. Rev. Entomol. 2015, 60, 17–34. [Google Scholar] [CrossRef] [Green Version]
- Handley, M.A.; Hall, C.; Sanford, E.; Diaz, E.; Gonzalez-Mendez, E.; Drace, K.; Wilson, R.; Villalobos, M.; Croughan, M. Globalization, Binational Communities, and Imported Food Risks: Results of an Outbreak Investigation of Lead Poisoning in Monterey County, California. Am. J. Public Health 2007, 97, 900–906. [Google Scholar] [CrossRef]
- Zhuang, P.; Zou, H.; Shu, W. Biotransfer of Heavy Metals along a Soil-Plant-Insect-Chicken Food Chain: Field Study. J. Environ. Sci. 2009, 21, 849–853. [Google Scholar] [CrossRef]
- Lesnik, J.J. Not Just a Fallback Food: Global Patterns of Insect Consumption Related to Geography, Not Agriculture. Am. J. Hum. Biol. 2017, 29, e22976. [Google Scholar] [CrossRef]
- Park, S.; Yun, E. Edible Insect Food: Current Scenario and Future Perspectives. 축산식품과학과 산업 2018, 7, 12–20. Available online: https://www.koreascience.or.kr/article/JAKO201820159112036.pdf (accessed on 30 September 2021).
- Grafton, R.Q.; Daugbjerg, C.; Qureshi, M.E. Towards Food Security by 2050. Food Secur. 2015, 7, 179–183. [Google Scholar] [CrossRef]
- Belluco, S.; Losasso, C.; Maggioletti, M.; Alonzi, C.C.; Paoletti, M.G.; Ricci, A. Edible Insects in a Food Safety and Nutritional Perspective: A Critical Review. Compr. Rev. Food Sci. Food Saf. 2013, 12, 296–313. [Google Scholar] [CrossRef]
- Dobermann, D.; Swift, J.A.; Field, L.M. Opportunities and Hurdles of Edible Insects for Food and Feed. Nutr. Bull. 2017, 42, 293–308. [Google Scholar] [CrossRef] [Green Version]
- Kim, T.-K.; Yong, H.I.; Kim, Y.-B.; Kim, H.-W.; Choi, Y.-S. Edible Insects as a Protein Source: A Review of Public Perception, Processing Technology, and Research Trends. Food Sci. Anim. Resour. 2019, 39, 521–540. [Google Scholar] [CrossRef] [Green Version]
- Patel, S.; Suleria, H.A.R.; Rauf, A. Edible Insects as Innovative Foods: Nutritional and Functional Assessments. Trends Food Sci. Technol. 2019, 86, 352–359. [Google Scholar] [CrossRef]
- Niles, M.T.; Bertmann, F.; Belarmino, E.H.; Wentworth, T.; Biehl, E.; Neff, R. The Early Food Insecurity Impacts of COVID-19. Nutrients 2020, 12, 2096. [Google Scholar] [CrossRef]
- Gahukar, R. Entomophagy and Human Food Security. Int. J. Trop. Insect Sci. 2011, 31, 129–144. [Google Scholar] [CrossRef] [Green Version]
- van Huis, A. Edible Insects Contributing to Food Security? Agric. Food Secur. 2015, 4, 20. [Google Scholar] [CrossRef] [Green Version]
- Rumpold, B.A.; Schlüter, O.K. Nutritional Composition and Safety Aspects of Edible Insects. Mol. Nutr. Food Res. 2013, 57, 802–823. [Google Scholar] [CrossRef]
Factors | Description |
---|---|
Feed | Various organic wastes, such as manure, food waste, and industrial organic byproducts, have different compositions and may require varying fermentative preprocessing actions and chemoattractant treatment for H. illucens. |
pH | The acidity and alkalinity of the organic waste affects the microbiota, thereby affecting the potential preprocessing or fermentation that can influence the development of H. illucens. |
Moisture | The moisture content of the feed can affect the rate of consumption. The larvae of H. illucens lack teeth and have preferred moisture levels. Excessive moisture influences microbial growth as well as the larval growth rate. Moisture plays a more important role in the development and survival of H. illucens than the protein and carbohydrate content of feed. Larvae were found to be unable to develop on diets with 30–40% moisture content, with most larvae dying within 13 days [19,20]. |
Temperature | The environmental temperature affects the survival rate and growth rate/metabolism of H. illucens and microbes, in turn affecting the speed of consumption and digestion. A favourable temperature is 30 °C. |
Size of Container | Overcrowding can negatively impact the developmental stages and survival of H. illucens. In a small container, there was an overall 28.8% lower survivorship than in a large rearing tray at 24.7%, with the larvae also growing to a larger sizes in the larger tray. However, the bioconversion rate in the large tray was only 2.7% higher than that in the smaller container [21]. |
Species strain | The strain of H. illucens underpins its developmental time and ability to reduce dry matter [21]. A comparison of three strains (Texas strain; Guangzhou strain; Wuhan strain) showed that they reduced poultry manure by 56.8%, 31.8%, and 61.7%, respectively. |
Severe food limitations | The most substantial food limitation at high density (200 and 400 larvae consumed 0.09 and 0.06 g per larva, respectively) kept H. illucens at the prepupal stage for 45 days. Overcrowding delayed metamorphosis, perhaps because of nutrient limitations. Comparisons between batch and daily feeding showed daily feeding to provide better weight gain but result in a longer prepupal stage [22]. Furthermore, severe food limitations were found to prolong or pause larval development time. |
Microbial environment | Bacterial species isolated from H. illucens eggs and from the larval gut that were further inoculated into chicken manure with pre-existing H. illucens larvae independently promoted H. illucens larval growth. Larvae reared in manure with the species Kocuria marina, Lynsinibacillus boronitolerans, Proteus mirabilis, and Bacillus subtilis had higher weight gain and manure reduction rates compared to the control without supplementation [23]. Supplementation with Bacillus subtilis was also found to lead to faster manure processing [24]. |
No. | Challenge |
---|---|
1 | Precision, reliability, and efficiency of operating the H. illucens nursery to maximize young larva production for higher survival rates. |
2 | The economical scale of technologies [11,12,27]—the supply chains for the input of waste and distribution of extracted products and frass for various industries are still lacking. For example, the processing of animal feed in one location and the sending of the frass to nearby farms and agricultural land may be a logistical challenge. |
3 | Missing benchmarks for products—the full benefits of H. illucens larval-based feeds and frass have still to be extensively demonstrated and benchmarked, therefore facing market penetration challenges. |
4 | Incomplete or restrictive local regulations on usage—Several countries have started allowing the use of H. illucens larvae for the production of feeds under certain strict conditions (registration, processing, animal specificity) [11]. However, some countries still prohibit its use as feeds for livestock that are meant for later consumption by humans [27]. Given the general novelty of this approach, there may be regions with blanket prohibitions on it from the lack of established guidelines. |
5 | Containment of H. illucens to prevent escape—this is challenging because the adult fly is able to escape by flying away, requiring that a more secured containment area. |
6 | Hermetia illucens larva consumption rate can vary between different biowaste types. Most experiments have been performed in small scale, with unknown scalability and sustainability for larger applications [27]. With each batch of biowaste that comes in for H. illucens larva treatment having different compositions, the results of experiments can vary significantly. |
Organic Waste | Origin |
---|---|
Human manure | Faecal sludge from sewage |
Animal manure | Farms with poultry, cow, or swine |
Fruit wastes | Discarded/rotten fruits from food companies or markets |
Vegetable wastes | Spoilt/rotten vegetables from farms, food companies, or markets |
Municipal organic solid wastes | Food scraps from households, restaurants, markets, malls, companies, and public institutions |
Millings and brewery side streams | From the milling and brewery industries, dried distiller grains, wheat, bran, billed grains, and grinding dust |
Poultry feeds | Uneaten feeds used for poultry |
Life Cycle Stage | Crude Protein Percentage |
---|---|
Larval phase | ~38% |
Matured larva (Day 14) | ~39.2% |
Early pupa | ~46.2% |
Post-mortem adult | ~57.6% |
Composition of T. molitor | Description |
---|---|
Crude protein | The crude protein content of larvae is 52.4% in average and ranges from 47.0 to 60.2% [58]. Tenebrio molitor larvae have high quantities of high-quality amino acids and are thus a highly sustainable protein source alternative. |
Crude fibre | The whole insect contains a variable amount of fibre, including crude fibre, acid detergent fibre, and neutral detergent fibre [61,62,63]. The crude fibre content of T. molitor larvae averages 7.43% and ranges from 4.19 to 22.35%. The average crude fibre content of the larvae is higher than that of fishmeal (0.26%) [58]. |
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations. |
© 2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
Share and Cite
Kuan, Z.-J.; Chan, B.K.-N.; Gan, S.K.-E. Worming the Circular Economy for Biowaste and Plastics: Hermetia illucens, Tenebrio molitor, and Zophobas morio. Sustainability 2022, 14, 1594. https://doi.org/10.3390/su14031594
Kuan Z-J, Chan BK-N, Gan SK-E. Worming the Circular Economy for Biowaste and Plastics: Hermetia illucens, Tenebrio molitor, and Zophobas morio. Sustainability. 2022; 14(3):1594. https://doi.org/10.3390/su14031594
Chicago/Turabian StyleKuan, Zhi-Jue, Barnabas Kuan-Nang Chan, and Samuel Ken-En Gan. 2022. "Worming the Circular Economy for Biowaste and Plastics: Hermetia illucens, Tenebrio molitor, and Zophobas morio" Sustainability 14, no. 3: 1594. https://doi.org/10.3390/su14031594
APA StyleKuan, Z. -J., Chan, B. K. -N., & Gan, S. K. -E. (2022). Worming the Circular Economy for Biowaste and Plastics: Hermetia illucens, Tenebrio molitor, and Zophobas morio. Sustainability, 14(3), 1594. https://doi.org/10.3390/su14031594