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Article

Valorisation of Organic Waste By-Products Using Black Soldier Fly (Hermetia illucens) as a Bio-Convertor

1
Institute of Life Course and Medical Sciences, University of Liverpool, Liverpool L1 8JX, UK
2
AgriGrub Ltd., NIAB Innovation Hub, Hasse Road, Soham, Cambridgeshire CB7 5UW, UK
3
Inspro Ltd. Brook House, Mead Road, Cranleigh, Surrey GU6 7BG, UK
*
Author to whom correspondence should be addressed.
Sustainability 2021, 13(15), 8345; https://0-doi-org.brum.beds.ac.uk/10.3390/su13158345
Submission received: 28 June 2021 / Revised: 19 July 2021 / Accepted: 23 July 2021 / Published: 27 July 2021
(This article belongs to the Special Issue Sustainable Food Production and Consumption)

Abstract

:
One third of food produced globally is wasted. Disposal of this waste is costly and is an example of poor resource management in the face of elevated environmental concerns and increasing food demand. Providing this waste as feedstock for black soldier fly (Hermetia illucens) larvae (BSFL) has the potential for bio-conversion and valorisation by production of useful feed materials and fertilisers. We raised BSFL under optimal conditions (28 °C and 70% relative humidity) on seven UK pre-consumer food waste-stream materials: fish trimmings, sugar-beet pulp, bakery waste, fruit and vegetable waste, cheese waste, fish feed waste and brewer’s grains and yeast. The nutritional quality of the resulting BSFL meals and frass fertiliser were then analysed. In all cases, the volume of waste was reduced (37–79%) and meals containing high quality protein and lipid sources (44.1 ± 4.57% and 35.4 ± 4.12%, respectively) and frass with an NPK of 4.9-2.6-1.7 were produced. This shows the potential value of BSFL as a bio-convertor for the effective management of food waste.

1. Introduction

It is estimated that the human population will exceed 9 billion by 2050. An increase in food production of around 50% will be needed to meet their needs [1]. Despite this rising demand, one third of all food produced globally is lost or wasted, equating to approximately 1.3 billion tonnes per year [2]. In the UK alone, 10.2 million tonnes of food waste was generated in 2015, of which 7.1 million tonnes was household waste and the remaining 3.1 million tonnes was from the post farm-gate supply chain [3]. The ‘waste hierarchy’ [4] illustrates destinations for waste ranked by environmental impact: prevention and minimisation (of waste generation such as redistribution), reuse (for other purposes, including use as animal feed and biomaterial processing), recycling (including composting and anaerobic digestion), energy recovery (including incineration for heat generation) and, finally, disposal. This hierarchy has been incorporated into UK law though the Waste (England and Wales) Regulations 2011, the Waste Regulations (Northern Ireland) 2011 and the Waste (Scotland) Regulations 2012 [5]. According to the waste hierarchy, prevention and redistribution have the lowest environmental impact; however, once food has started to spoil, recycling becomes the next best option. Anaerobic digestion (AD) is a go-to technology favoured globally for recycling food and other organic waste into bioenergy. However, these systems suffer from poor stability and low efficiency, due to the characteristics of food waste [6].
Some food waste can be recycled to make animal feed (within certain confines of the law). Bakery or confectionery products, providing they do not contain and or have not been in contact with meat, fish, or shellfish, can be used. Food or catering waste from kitchens which process meat, vegetarian kitchens which handle dairy products, restaurants and commercial kitchens producing vegan food and international catering waste cannot be used [7]. Animal by-products (ABPs) are subject to greater restrictions to maintain safe food supply chains and appropriate management of high-risk materials. ABPs are divided into three categories, categories one and two being high risk materials, while category three are low risk; category three materials can be processed into farm animal or pet feeds, among other products [8].
There is a growing interest in the use of insects as natural bio-convertors of organic waste valorising the waste by consuming the waste, incorporating it into their bodies and, in the process, converting it into valuable products. Life cycle assessment (LCA) has shown that insect bio-conversion is efficient and environmentally sustainable; direct greenhouse gas (GHG) emissions produced by insects are 47 times lower and the resulting global warming potential (GWP) is half that of open air composting [9]. Production of insects as a food also uses comparatively little space (reducing land use), but, usually, has a relatively high energy use (and GWP) for heating, to achieve a suitable culture environment and for drying the insects after harvest. This high energy demand may be exacerbated by the need to transport the food source to an insect production facility [10]. Overall, energy consumption can be reduced by using waste heat from other industrial processes, or using AD or incineration of other low category waste to heat the system [11]. Insect products can replace less sustainable products, such as fishmeal or soy products in aquaculture feeds; if this product replacement is also accounted for during LCA assessment, then the GWP of insect production decreases further [9,10].
Insects have previously been used in organic waste management strategies, recovering nutrients in the form of the constituent parts of the insect yielding high quality protein, lipid and chitin [12,13,14,15]. Insects, or their derivative proteins and fats, are utilized as food for humans [16,17] and in animal feeds [18,19]. Further, as a lipid-rich source, they can also be used for the production of biodiesel [10]. In this paper we focus primarily on the value of the products as constituents of animal feed.
Of the many insect species that have been studied [16,17], the black soldier fly (BSF) (Hermetia illucens) stands out. It has many characteristics that make it particularly attractive for commercial scale production in the UK. It is a species of true fly (Diptera) of the family Stratiomyidae. It originates from the Americas, although they are now more widespread in tropical and temperate regions [20,21,22,23]. They do not tolerate colder climates, such as those found in north-western Europe [24]. Therefore, if any escape from culture facilities, they are unlikely to survive the winter and become an invasive species. The BSF larvae (BSFL) are capable of consuming a wider range of organic materials than other fly species [25,26]. The adult stage is not a vector for human, animal, or plant pathogens. It does not possess mouth apparatus, so cannot bite [25,27,28]. BSF have an excellent nutritional profile, high in protein with a high quality amino acid profile and high levels of lipid, including economically and nutritionally valuable fatty acids [25]. Hermetia illucens was included in the seven insect species listed in the Commission Regulation (EU) 2017/893 [29] as safe for production for food use. This regulation permits the use of processed animal proteins (PAPs) derived from those insect species for aquaculture feeds, pet feeds and fur animal feeds in the EU. Insects grown for the production of processed insect proteins (PIPs) that are fed to other farmed animals are categorized as ‘farmed animals’ (Article 3(6) of Regulation (EC) No 1069/2009; [30]). As such, they are subject to regulations in the use of feed materials used to grow them [31]. The fact that they can be used in aquaculture feeds, their high-quality nutritional profile and their utility for bioconversion of waste strongly suggest that there will be an increase in the demand for BSFL and BSFL products.
Production of BSFL PIPs involves hatching BSFL, then growing them on an organic feed material, until they reach an appropriate life stage. They are then separated from the remains of the feed and larval residue (known as frass) and harvested. BSFL products have several potential uses, the primary use, that we discuss here, is the production of meal. Liu and Chen [32] concluded the early pre-pupae is the most appropriate life stage to harvest for meal production. This stage was, therefore, used during this study. BSFL meal can be further processed to concentrate protein while extracting the lipids for other uses as high-quality feed ingredients. In addition, lipids can also be used for biodiesel production [33] and chitin can be extracted from the meal for many uses, including food, pharmaceuticals, textiles, waste water treatment and cosmetics [34]. The BSFL lipid content is of particular interest because of the high content (approximately 28.6 ± 8.6% of insect mass) and because it is rich in useful fatty acids [25]. Spranghers and Ottoboni [14] showed that the fatty acid profile of BSFL is highly influenced by their diet, highlighting an opportunity for manipulation of the product via diet.
The ‘frass’ is a by-product that consists of faecal matter, residual growing substrate and shed exoskeletons from previous instars. It has value as a good quality, slow release organic fertiliser, with higher NPK values than other animal by-products recognized as fertilizers, such as composted poultry litter and worm castings [35]. Frass can also be processed via AD for further energy recovery, as it possesses suitable characteristics [36]. The anaerobic biodegradability fraction (fd) of BSFL frass is equal to that of food waste (89%); however, it has higher bio-methane potential (502 ± 9 mL CH4/g VS) than food waste (449 ± 53 mL CH4/g VS) [36]. Food waste also causes two main problems for AD, poor stability, due to volatile fatty acids and low organic loading rates and effectively low efficiency [37,38], caused by high levels of easily biodegradable suspended solids [6]. However, significantly, utilising BSFL to bio-convert food waste into high quality feed ingredients can be classed as “prevention”; therefore, it is preferred over AD as a method for processing organic food waste in the waste hierarchy [4,39].
The increased interest in the use of BSFL as an organic waste management tool and a source of raw materials for the manufacture of animal feed has led to a better understanding of how nutrient density and feed substrate quality can influence the development and growth of BSFL [40,41]. BSFL have been shown to achieve a good feed conversion ratio (FCR), ranging between 1.4 and 2.6, when fed food waste materials [42]. Diets consisting of high protein and high lipid achieve the best results. The nutritional profile of the end larval material is also affected and, while protein levels do vary, the lipid levels and profile are more highly affected [14,43]. In this study, we look at the impact of seven potential organic waste streams (Table 1) from pre-consumer and manufacturing situations on BSFL bio-concentration of nutrients and, primarily, fatty acids. We evaluate which of our organic waste materials are most suitable for use in modulating and manipulating fatty acid profiles of BSFL meal and draw conclusions about the valorisation of organic waste by-products via BSFL treatment.
In response to the change in EU law [29] allowing use of insect meals and the growing interest in this area, it is very likely that these meals will become highly valued as aquaculture feed ingredients. Because fish lack the enzymes to completely synthesize polyunsaturated fatty acids (PUFA), or highly unsaturated fatty acids (HUFA) of the n-3 and n-6 series de novo [44], these must be provided preformed via the diet, making them essential fatty acids (EFAs): linoleic acid (18:2n-6), α-linolenic acid (18:3n-3), arachidonic acid (20:4n-6), Eicosapentaenoic acid (EPA, 20:5n-3) and Docosahexaenoic acid (DHA, 22:6n-3) [45]. This study pays close attention to these EFAs and their potential as feed ingredients.

2. Materials and Methods

2.1. Outcomes

2.1.1. Growth Performance of BSFL Fed Identified Organic Materials

BSFL are produced under optimal conditions, fed on our identified feed materials and converted into BSFL meals. Growth performance is assessed to explore BSFL meal production and waste reduction potential of each organic material.

2.1.2. BSFL Bioconcentration and Modification of Fatty Acid Profile

Samples of feed materials and BSFL meals were collected and analysed for nutritional quality—protein, lipid and fatty acid profiles. Data were analysed to assess bioconcentration of nutrients during production of BSFL meals, in order to identify suitable organic by-products for nutrient recovery by BSFL.

2.1.3. Valorisation of Organic Waste By-Products via BSFL Treatment

The value of the BSFL outputs, meals and frass, was estimated to assess valorisation of the identified organic waste streams via BSFL treatment.

2.2. Processing Organic Waste Materials

Water was added to the sugar beet, bakery waste, cheese waste and fish feed waste to achieve 70% water content prior to feeding, while the fish trimmings, fruit and vegetable waste and brewer’s grains and yeast already contained a high enough water content. All feedstock materials were homogenized, prior to feeding, in order to optimize processing by BSFL. Samples (100 g) of each material were frozen at −20 °C and sent to Nottingham University for proximate analyses and fatty acid analyses.
Material energy content was determined using a Parr 6300 bomb calorimeter connected to a Parr 6520 water recirculation system. One-gram Benzoic acid tablets standardized for bomb calorimetry (26.454 MJ/kg, Parr Instrument Co, item No: 3415) were used as standards. Material protein content was analysed using a Thermo Scientific FlashEA® 1112 N/Protein Analyzer in conjunction with the EAGER software. The lipid content of each sample was analysed using rapid Soxhlet extraction, using a Gerhardt Soxtherm. The extracted lipid samples were further analysed to determine the fatty acid profile of each sample by applying a direct method for fatty acid methyl ester (FAME) synthesis, in conjunction with GC analyses (Perkin Elmer Clarus 500 Gas Chromatograph), utilizing a Varian capillary column CP-Sil 88 for FAME; column length, 100 m, column width, 0.25 mm. Gas flow for air was 450 mL/min and hydrogen was 45 mL/min; the temperature set point was 250 °C. Ash was determined using the AOAC official method 942.05 [48]. Fibre content was analysed using the Gerhardt Fibrebag method.

2.3. BSFL Production

Each of the experimental organic waste stream materials were fed to five replicate groups of 25 larvae, for a total of 35 groups of BSFL. Larvae were grown under environmentally controlled conditions (28 °C and 70% relative humidity) and kept in the dark during production. BSFL growth and performance were assessed through feed conversion ratio (FCR), specific growth rate (SGR) and larval growth rate (LGR). Efficiency of conversion of ingested food (ECI) was assessed. Waste material reduction was assessed through waste reduction index (WRI) and substrate reduction (SR). All using the following equations:
F C R = T F I   k g ÷ W e i g h t   g a i n   k g
where TFI (total feed intake) = total feed given and Weight gain = weight at end of study period–weight at start of study period [49].
S G R   % = 100 × ln W 2 ln W 1 × t 2 t 1 1
where ln = natural log, W1 = initial weight, W2 = final weight, t1 = starting time point (day one) and t2 = end time point (final day number) [50].
L G R   g / d a y = W 2 W 1 / n u m b e r   o f   d a y s
where W1 = initial larval weight (g), W2 = final larval weight (g) [51].
E C I = B W R
where B = total biomass (larvae) (g), W = total amount of feed provided (g) and R = remaining substrate (g) [51].
W R I = W R / W / d a y s   o f   t r i a l   d × 100
where W = total amount of feed provided and R = remaining substrate [51].
S R = W R W × 100
where W = total amount of feed provided and R = remaining substrate [51].

2.4. Nutritional Analyses of BSFL Pre-Pupae Fed Each Organic Material

BSFL groups were harvested at the pre-pupae stage and frozen at −20 °C. They were dried in a drying cabinet at 60 °C for 4 days, then ground into BSFL meal using a benchtop hand grinder. Samples of each meal were sent to Skretting UK for analysis—crude protein, crude lipid, amino acid profile and fatty acid profile. The BSFL meal nutrient content for crude protein, crude lipid and fatty acids were analysed as the feed materials above. Amino acid profiles were determined using hydrolyses and an amino acid analyser. These data were combined with Skretting UK’s undisclosed data regarding protein digestibility of BSFL meal for value estimation as an aquaculture feed ingredient.

2.5. Data Analyses

A representative frass sample was collected during production of the BSFL and analysed by NMR laboratories for nitrogen (N), phosphorus (P), potassium (K) (NPK) and magnesium (Mg) to assess the quality of the waste product for use as a fertiliser.
Nutrient bioconcentration by BSFL from each of the organic waste materials was investigated by generating an apparent bioconcentration factor (aBCF) for each nutrient, i.e., crude protein, crude lipid, fatty acids and fatty acid groups, which are present in both feed materials and BSFL meals, calculated as follows:
a B C F i = F A i T D F A B S F L   m e a l F A i T D F A D i e t         or         a B C F i = N u t r i e n t i B S F L   m e a l N u t r i e n t i D i e t
where i = specific FA (g/100 g DM), or the sum of a group of FA (SFA, MUFA, MUFA trans, PUFA and branched FA) and TDFA = total detected fatty acids (g/100 g DM), or nutrient (g/100 g DM of crude protein or crude lipid) [43].

2.6. Value Estimation of BSFL Outputs

Each BSFL meal was inputted into Skretting’s aquaculture feed formulation software programme; this programme assigned a value to each BSFL meal (as an ingredient), based on their nutritional qualities compared to the quality of all the other available feed ingredients and their current market prices (correct as of February 2019). The potential value of frass can be estimated based on N, P and K content along with current costs of those nutrients available through other marketed fertilisers, as described by Kissel and Risse [52].

2.7. Statistical Analysis

Tests for differences were carried out with 95% confidence levels (p ≤ 0.05) between each test substance. The Kolmogorov–Smirnov tests for normality were carried out, with one-way ANOVA tests, followed by post hoc Tukey’s tests, used for parametric data, and Mann–Whitney U tests, for non-parametric data.

3. Results

3.1. BSFL Growth, Performance and Substrate Reduction

Growth and performance of the BSFL varied significantly depending on the feedstock they were fed (Table 2). Sugar beet pulp and cheese waste were used the least efficiently by BSFL, attaining the lowest ECI, LGR and SGR, subsequently reaching the highest FCR. Bakery waste achieved the greatest performance (FCR and SGR), while fish feed waste was the most efficiently used (ECI). The BSFL consumed more cheese waste (WRI) than any other feedstock. The greatest reduction in feedstock substrate (SR) was seen with fruit and vegetable waste. BSFL mortality rate when fed fish feed waste (48.8%) was significantly higher (p < 0.05) than when fed all other feedstocks (4–12%).

3.2. BSFL Nutrient Bioconcentration

3.2.1. Organic Waste Material and BSFL Meal Profiles

The variety of organic waste materials used display a range in protein (8.4–54.0 g/100 g DM) and lipid (0.4–57.3 g/100 g DM) levels (full nutritional profile of the BSFL meal provided in Appendix A). Each material also displays varied fatty acid profiles (Table 3).
The nutrient profiles of the BSFL meals (Table 4) were influenced by the different organic feed materials. However, there was less variation between the BSFL meals than there was between the organic waste stream materials, with average crude protein levels of 44.1% (±4.57) and lipid levels of 35.4% (±4.12), compared to 30.48% (±19.11) and 16.48% (±21.86). Leucine, aspartic acid and glutamic acid were the three most prevalent amino acids across all the BSFL meals, with tyrosine being exceptionally higher in BSFL fed cheese waste, fish feed waste and brewer’s grain and yeast. The fatty acids most prevalent across all the BSFL meals included Lauric acid, Myristic acid, Palmitic acid, Palmitoleic acid, Oleic acid and linoleic acid. BSFL fed fish trimmings also contained raised levels of EPA. BSFL fed brewer’s grains contained the highest level of n6 fatty acids with a high level of n3 fatty acids, containing EFA’s linoleic and α-linolenic acid, alongside a good level of EPA and small amounts of DHA, with only the fish trimmings and fish feed waste fed BSFL meals possessing higher levels of EPA and DHA.

3.2.2. BSFL Bioconcentration of Nutrients

According to the method used to calculate aBCF, values higher than unity are considered to indicate nutrient concentration. These results show that BSFL bioconcentrate nutrients from most organic food materials very well. Lauric acid is the fatty acid which BSFL accumulate the greatest across all feed materials (Table 5). BSFL fed cheese waste is the only meal where lauric acid is not the most bioconcentrated FA; EPA is higher. BSFL achieve the greatest bioconcentration of the overall desired EFAs from fish trimmings, followed by brewer’s grains and cheese waste.

3.3. Valorisation of BSFL Products

3.3.1. Value of BSFL Meals as Aquaculture Feed Ingredients

The predicted value of each BSFL meal, as feed ingredients within the aquaculture feed market, based on nutritional quality, is as follows:
  • BSFL fed fish trimmings = GBP 824 per tonne
  • BSFL fed sugar beet pulp = GBP 743 per tonne
  • BSFL fed bakery waste = GBP 792 per tonne
  • BSFL fed fruit and vegetable = GBP 792 per tonne
  • BSFL fed cheese waste = GBP 787 per tonne
  • BSFL fed fish feed waste = GBP 822 per tonne
  • BSFL fed brewer’s grains and yeast = GBP 819 per tonne
(correct as of February 2019).

3.3.2. Quality and Value of BSFL Frass

Analyses of the BSFL frass revealed a magnesium level of 0.26% (2589 mg/kg) and an NPK of 4.9-2.6-1.7. Therefore, it would take approximately 5 tonnes of dry material or 8 tonnes of wet material (62.4% DM) to reach a maximum fertilizer application rate of 250 kg/ha of nitrogen. The BSFL frass contains high NPK levels compared to other manure fertilisers (Table 6). Utilising other fertiliser prices and NPK content (Table 7), the BSFL frass has been estimated to be worth a value of GBP 57.12/tonne. When the value of other manure fertilisers is calculated using the midpoint values for NPK taken from Table 5, the BSFL frass compares very favourable, achieving the highest value (Table 8).

4. Discussion

The results achieved here clearly concur with that of other studies [32,55]—the nutritional profile of BSFL is highly influenced by their diet.
Protein is frequently the most expensive component of agricultural diets, especially in aquaculture diets [56]. The BSFL meals produced here are high in crude protein (>43%), except when produced using fruit and vegetable waste (36%). This level reaches as high as 51% when produced using brewer’s grains. These meals are rich in the amino acids leucine, aspartic acid and glutamic acid and very rich in tyrosine, when produced with cheese waste, fish feed waste and brewer’s grains, on an % DM basis. Fishmeal is considered a very high-quality protein source for aquaculture diets [57]. Compared to an average 65% (70.7% DM) seen in fishmeal [58], the quality of this BSFL meal is also high, with a well-balanced amino acid profile. However, BSFL meal contains relatively lower levels of the three common limiting amino acids, arginine, lysine and methionine, although levels of the latter two are still good; however, it is richer in histidine, isoleucine, phenylalanine, tyrosine, valine, alanine and proline, on a percentage protein basis (Table A1a). Soybean meal is the most commonly used plant protein in aquaculture feeds, despite its nutritional restrictions [59,60,61]. The BSFL meals are overall richer in the amino acids alanine, glycine, histidine, methionine, proline and valine, compared to high protein soybean meal [62], on a percentage protein basis (Table A1a).
The fatty acid profile is the nutritional aspect of the BSFL meal most affected by diet. The most prevalent fatty acids across all BSFL meals are lauric acid, oleic acid, palmitic acid and linoleic acid, both on a % DM (Table 3b) and % total fatty acid basis (Table A1b), although they do vary considerably, depending on the BSFL food source.
Lauric acid, the most prevalent fatty acid found in BSF meal, is credited with antimicrobial, antiviral and antifungal properties [63,64,65]. It has been shown to reduce Campylobacter spp. in broilers [66]. The other most abundant fatty acids found here also have many uses, including use in food [67], as emulsifiers in soap [68], as emollients in cosmetics [69] and as excipients in pharmaceuticals [67]. A high level of linoleic acid, which also has been credited with antimicrobial properties [70], along with the other essential FAs, is desirable in agriculture and aquaculture feed ingredients for many species.
The bioconcentration data we present indicate how efficiently each nutrient is recovered from the organic materials by BSFL treatment. The bioconcentration of each nutritional element varies with each organic feed stock. BSFL fed on fruit and vegetable waste had high EPA conversion rates; however, the final amount of EPA remained low in the BSFL meal, because the EPA levels were low in the fruit and vegetable waste material. The highest conversion rates for the essential fatty acids is seen in BSFL fed on fish trimmings, cheese waste and brewer’s grains. BSFL fed fish trimmings and brewer’s grains also had the highest levels of essential FAs. These food waste feed stocks, therefore, are likely the most viable that we tested for production of feed ingredients for use in aquaculture or agriculture feeds. The BSFL that were fed fish feed waste also had high levels of these essential FAs; however, the bioconcentration factor was low (viz. there was no apparent concentration during BSFL treatment), so the high levels of essential FAs were due to the high levels of these nutrients in the fish feed waste material.
These results provide evidence that manipulation of the fatty acid profile is achievable via diet. The BSFL meal that was produced, beyond use in feeds, has several possibilities for further refinement, such as lipid extraction. The high lipid content of BSFL meal, once extracted, would be suitable feedstock for biodiesel production [33]; BSFL that were fed fruit and vegetable waste generated the highest lipid levels. This meal also has the lowest crude protein level achieved here. While a detailed examination is beyond the scope of this study, we could speculate that lipid extraction would also provide an improved protein meal, as well as the richest biodiesel lipid feedstock.
Depending on the target nutrient or product and target use, we have identified several industrial and pre-consumer organic by-products that could be processed via BSFL treatment and provided data to show which of these generate high-value nutrients for feed production or other added value products, instead of simply sending this “food waste” for AD, composting, landfill, or incineration.
We have shown that all of our selected organic waste materials can be utilised as feedstock by BSFL; however, our growth and performance data indicate which are most suitable to accomplish higher levels of production of BSFL products. In all cases, waste reduction (DM basis) was achieved. Therefore, BSFL treatment could be a viable method of reducing all these pre-consumer organic waste materials, generating lower volumes of more valuable and accessible materials.
BSFL treatment, as well as being more sustainable according to the waste hierarchy, clearly provides opportunities for increased valorisation of organic by-products, especially as the frass produced from BSFL treatment is more suitable than many organic food materials for AD treatment, or, as discussed, has value as fertiliser. The value calculated here is purely based on NPK content compared to the costs of other manure fertilisers. However, when looking to source BSFL frass fertilisers, they attract a considerably higher value than that of its NPK content would suggest; Ecothrive charge is a frass soil conditioner selling at GBP 29.95 per 3.5 kg, which scales to GBP 8557.14 per tonne (correct as of April 2020 [71]), a vastly improved value from the estimated GBP 57 per tonne. BSFL frass qualities which contribute to this high value include slow release of nutrients, support of soil microbiota [72] and promotion of plant health and growth; BSFL frass has also indicated insecticidal properties against wireworm [35].

5. Conclusions

This study shows how seven organic waste by-products influence the nutritional profile of BSFL. We identify that fish feed trimmings, along with brewer’s grains and yeast, are ideal organic waste materials for BSFL treatment in order to generate high quality BSFL meals which would be suitable for inclusion in aquaculture or agriculture feeds. We have also identified that fruit and vegetable waste is a potential candidate for BSFL treatment, followed by lipid extraction, for recovery and production of lipid feedstock for biodiesel due to the higher lipid content.
BSFL treatment is a viable option for recovering and recycling organic waste by-products, especially if it is traceable to source. It provides opportunity for the valorisation of these organic waste products as constituents of animal feed, providing a more environmentally friendly alternative route than landfill or AD.

Author Contributions

Conceptualization, I.Y. and R.S.; methodology, K.M., J.H.; validation, J.H.; formal analysis, K.M.; investigation, K.M. and J.H.; resources, R.S., J.H. and I.Y.; data curation, K.M.; writing—original draft preparation, K.M.; writing—review and editing, K.M., I.Y.; visualization, K.M.; supervision, K.M. and I.Y.; project administration, I.Y. and R.S.; funding acquisition, I.Y. and R.S. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by Innovate UK, grant number 7714.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not Applicable.

Data Availability Statement

Not Applicable.

Acknowledgments

We would like to acknowledge the following for their contributions to our research: Tim Parr and Jon Stubberfield at the School of Biosciences, University of Nottingham, Sutton Bonington Campus, Loughborough for providing analysis, in kind, of the seven organic waste stream materials we trialled. Skretting UK for provision of the waste fish feed material, for providing nutritional analyses of the BSFL meals and for utilising their feed formulation software to associate a value of the BSFL meals as aquaculture feed ingredients based on their quality. Sarah Gaunt and SPG innovation Ltd. were pivotal in navigation of the funding landscape to help us deliver proof of concept projects for our innovative technologies.

Conflicts of Interest

Mr Richard Small is the owner/CEO of Inspro Ltd.—a company that aims to become a supplier of BSFL meal. All other authors declare no conflict of interest.

Appendix A

Table A1. (a) Nutritional profile of BSFL meals, amino acid given as % protein, compared to an average 65% fishmeal and an average high protein soybean meal. (b) Nutritional profile of BSFL meals, fatty acids given as % total fatty acids, compared to an average 65% fishmeal and an average high protein soybean meal.
Table A1. (a) Nutritional profile of BSFL meals, amino acid given as % protein, compared to an average 65% fishmeal and an average high protein soybean meal. (b) Nutritional profile of BSFL meals, fatty acids given as % total fatty acids, compared to an average 65% fishmeal and an average high protein soybean meal.
(a)
Diet ComponentAverage 65% Protein FishmealHigh Protein Soybean MealFish TrimmingsSugar Beet PulpBakery WasteFruit and Vegetable WasteCheese WasteFish Feed WasteBrewer’s Grains and Yeast
Proximate analyses (% DM)Crude Protein (% DM)70.755.246.6243.1543.0736.0343.1845.751.05
Lipid (crude fat) (% DM)101.735.0535.4937.6340.336.9435.2227
Essential amino acids (% protein)Arginine (Arg)6.217.304.424.154.273.974.524.683.84
Histidine (His) 2.502.73.073.113.042.803.013.152.62
Isoleucine (Ile)4.144.64.234.264.094.024.214.354.13
Leucine (Leu)7.177.78.268.306.486.336.606.896.46
Lysine (Lys)7.506.25.175.085.605.475.515.546.17
Methionine (Met)2.721.41.871.811.831.751.901.751.67
Cystine (Cys)0.861.60.620.630.770.800.530.480.72
Phenylalanine (Phe)3.905.13.713.924.204.194.284.494.78
Tyrosine (Tyr)3.043.54.354.434.554.1112.2312.5410.66
Threonine (Thr)4.143.83.603.623.743.553.803.943.76
Tryptophan (Try/Trp)1.001.4-------
Valine (Val)4.984.85.735.846.085.866.116.375.95
Non-essential amino acids (% protein)Alanine (Ala)6.294.36.316.776.526.556.396.378.74
Aspartic acid (Asp)9.0911.38.288.719.038.608.559.027.93
Glutamic acid (Glu)12.5717.99.599.8710.159.6610.199.6310.05
Glycine (Gly)6.654.25.565.455.465.115.495.715.19
Proline (Pro)4.3455.685.725.395.306.676.506.56
Serine (Ser)3.894.63.934.013.953.693.914.003.80
Tryptophan was not analysed.
(b)
Diet ComponentAverage 65% Protein FishmealHigh Protein Soybean MealFish TrimmingsSugar Beet PulpBakery WasteFruit and Vegetable WasteCheese WasteFish Feed WasteBrewer’s Grains and Yeast
Essential fatty acids (% total fatty acids)C18:2n-6 (Linoleic acid)2.1546.533.615.614.093.445.6813.22
C18:3n-3 (α-linolenic acid)1.97.20.940.510.800.890.620.801.56
C20:4n-6 (Arachidonic acid)2.4 0.40<LOD<LOD0.100.140.090.07
C20:5n-3 (Eicosapentaenoic acid (EPA))9 3.420.250.110.200.492.211.96
C22:6n-3 (Docosahexaenoic acid (DHA))6.6 0.91<LOD<LOD<LOD<LOD0.170.26
Non-essential fatty acids (% total fatty acids)C8:0 (Caprylic acid) <LOD<LOD<LOD<LOD0.03<LOD<LOD
C10:0 (Capric acid) 0.970.990.900.691.001.360.85
C12:0 (Lauric acid) 35.9257.4052.6238.1933.4347.4426.59
C14:0 (Myristic acid)60.26.6510.4010.318.419.728.436.78
C14:1n-5 (Myristelaidic acid) 0.170.250.210.690.840.230.22
C15:0 (Pentadecanoic acid) 0.37<LOD0.110.200.600.170.30
C16:0 (Palmitic acid)17.811.213.4412.0912.6014.1920.0110.2517.04
C16:1n-7 (Palmitoleic acid)7.20.16.362.732.795.114.873.354.96
C16:2n-6 0.11<LOD<LOD<LOD<LOD0.06<LOD
C18:0 (Stearic acid)3.63.81.571.551.811.812.571.252.56
C18:1n-5 <LOD<LOD<LOD<LOD<LOD0.060.04
C18:1n-9 (Elaidic acid, Oleic acid)12.323.115.868.5110.6022.0118.0811.7315.67
C18:1n-7 (cis-vaccenic acid) 1.20<LOD0.290.300.620.741.41
C18:2n-4 <LOD<LOD<LOD<LOD0.110.03<LOD
C18:3n-6 (Gamma-linolenic acid (GLA)) 0.09<LOD<LOD<LOD0.050.030.04
C18:4n-3 (Stearidonic acid (SDA))1.5 0.66<LOD<LOD<LOD0.030.620.63
C20:0 (Arachidic acid) <LOD0.11<LOD<LOD0.080.090.22
C20:1n-8 0.26<LOD<LOD<LOD<LOD0.680.74
C20:1n-9 (Eicosenoic acid)6.6
C20:1n-11 (Gadoleic acid) 1.26<LOD<LOD<LOD0.300.971.11
C20:2n-6 (Eicosadienoic acid) <LOD<LOD<LOD<LOD0.190.200.22
C22:0 (Behenic acid) <LOD<LOD<LOD<LOD0.080.060.15
C22:1 n-9 (Erucic acid)7.7
C22:1n-11 (Cetoleic acid) <LOD<LOD<LOD<LOD<LOD0.340.26
C22:5n-3 (Docosapentaenoic acid (DPA))2.6
<LOD = below level of detection.

References

  1. FAO. The Future of Food and Agriculture–Trends and Challenges; Food and Agriculture Organization of the United Nations: Rome, Italy, 2017. [Google Scholar]
  2. FAO. Key Facts on Food Loss and Waste You Should Know! Save Food: Global Initiative on Food Loss and Waste Reduction. 2019. Available online: http://www.fao.org/save-food/resources/keyfindings/en/ (accessed on 12 March 2019).
  3. WRAP. Courtauld 2025 Signatory Data Report: 2015 and 2016; Harris, B., Ed.; WRAP: Banbury, UK, 2017. [Google Scholar]
  4. European Commission. Directive 2008/98/EC of The European Parliament and of The Council of 19 November 2008 on Waste and Repealing Certain Directives; Official Journal of the European Union: Aberdeen, UK, 2008. [Google Scholar]
  5. House of Commons; Environment, Food and Rural Affairs Committee. Food Waste in England, Eighth Report of Session 2016–2017; Environment, Food and Rural Affairs Committee’s Website: London, UK, 2017.
  6. Ye, M.; Liu, J.; Ma, C.; Li, Y.-Y.; Zou, L.; Qian, G.; Xu, Z.P. Improving the stability and efficiency of anaerobic digestion of food waste using additives: A critical review. J. Clean. Prod. 2018, 192, 316–326. [Google Scholar] [CrossRef] [Green Version]
  7. DEFRA. Statutory Guidance. Food and Drink Waste Hierarchy: Deal with Surplus and Waste. 2018. Available online: https://www.gov.uk/government/publications/food-and-drink-waste-hierarchy-deal-with-surplus-and-waste/food-and-drink-waste-hierarchy-deal-with-surplus-and-waste (accessed on 25 July 2021).
  8. DEFRA and APHA. Animal By-Product Categories, Site Approval, Hygiene and Disposal. 2018. Available online: https://www.gov.uk/guidance/animal-by-product-categories-site-approval-hygiene-and-disposal (accessed on 25 July 2021).
  9. Mertenat, A.; Diener, S.; Zurbrügg, C. Black Soldier Fly biowaste treatment–Assessment of global warming potential. Waste Manag. 2019, 84, 173–181. [Google Scholar] [CrossRef] [PubMed]
  10. Salomone, R.; Saija, G.; Mondello, G.; Giannetto, A.; Fasulo, S.; Savastano, D. Environmental Impact of Food Waste Bioconversion by Insects: Application of life Cycle Assessment to Process Using Hermetia illucens. J. Clean. Prod. 2017, 140, 890–905. [Google Scholar] [CrossRef]
  11. Lalander, C.; Nordberg, A.; Vinneras, B. A comparison in product-value potential in four treatment strategies for food waste and faeces, assessing composting, fly larvae composting and anaerobic digestion. GCB Bioenergy 2018, 10, 84–91. [Google Scholar] [CrossRef] [Green Version]
  12. Caligiani, A.; Marseglia, A.; Leni, G.; Baldassarre, S.; Maistrello, L.; Dossena, A.; Sforza, S. Composition of black soldier fly prepupae and systematic approaches for extraction and fractionation of proteins, lipids and chitin. Food Res. Int. 2018, 105, 812–820. [Google Scholar] [CrossRef] [PubMed]
  13. Sosa, D.A.T.; Fogliano, V. Potential of Insect-Derived Ingredients for Food Applications. In Insect Physiology and Ecology; Intech Open: London, UK, 2017; pp. 215–231. [Google Scholar]
  14. Spranghers, T.; Ottoboni, M.; Klootwijk, C.; Ovyn, A.; Deboosere, S.; Meulenaer, B.D.; Michiels, J.; Eeckhout, M.; Clercq, P.D.; Smet, S.D. Nutritional composition of black soldier fly (Hermetia illucens) prepupae reared on different organic waste substrates. J. Sci. Food Agric. 2017, 97, 2594–2600. [Google Scholar] [CrossRef]
  15. Wasko, A.; Bulak, P.; Polak-Berecka, M.; Nowak, K.; Polakowski, C.; Bieganowski, A. The first report of the physicochemical structure of chitin isolated from Hermetia illucens. Int. J. Biol. Macromol. 2016, 92, 316–320. [Google Scholar] [CrossRef]
  16. Rumpold, B.A.; Schluter, O.K. Potential and challenges of insects as an innovative source for food and feed production. Innov. Food Sci. Emerg. Technol. 2013, 17, 1–11. [Google Scholar] [CrossRef]
  17. Rumpold, B.A.; Schluter, O.K. Nutritional composition and safety aspects of edible insects. Mol. Nutr. Food Res. 2013, 57, 802–823. [Google Scholar] [CrossRef]
  18. Makkar, H.P.S.; Tran, G.; Heuze, V.; Ankers, P. State-of-the-art on use of insects as animal feed. Anim. Feed Sci. Technol. 2014, 197, 1–33. [Google Scholar] [CrossRef]
  19. Henry, M.; Gasco, L.; Piccolo, G.; Fountoulaki, E. Review on the use of insects in the diet of farmed fish: Past and future. Anim. Feed Sci. Technol. 2015, 203, 1–22. [Google Scholar] [CrossRef]
  20. Callan, E.M. Hermetia illucens (L.) (Dipt., Stratiomyidae), a cosmopolitan American species long established in Australia and New Zealand. Entomol. Mon. Mag. 1974, 109, 232–234. [Google Scholar]
  21. Kim, J.I. Newly recording two exotic insects species from Korea. J. Kor. Biota. 1997, 2, 223–225. [Google Scholar]
  22. May, B.M. The occurrence in New Zealand and the life-history of the soldier fly Hermetia illucens (L.) (Diptera: Stratiomyidae). New Zealand J. Sci. 1961, 4, 55–65. [Google Scholar]
  23. Üstüner, T.; Hasbenli, A.; Rozkosny, R. The first record of Hermetia illucens (Linnaeus, 1758) (Diptera, Stratiomyidae) from the Near East. Stud. Dipterol. 2003, 10, 181–185. [Google Scholar]
  24. Spranghers, T.; Noyez, A.; Schildermans, K.; Clercq, P.D. Cold Hardiness of the Black Soldier Fly (Diptera: Stratiomyidae). J. Econ. Entomol. 2017, 110, 1501–1507. [Google Scholar] [CrossRef]
  25. Wang, Y.-S.; Shelomi, M. Review of Black Soldier Fly (Hermetia illucens) as Animal Feed and Human Food. Foods 2017, 6, 91. [Google Scholar] [CrossRef] [Green Version]
  26. Kim, W.; Bae, S.; Park, K.; Lee, S.; Choi, Y.; Han, S.; Koh, Y. Biochemical characterization of digestive enzymes in the black soldier fly, Hermetia illucens (Diptera: Stratiomyidae). J. Asia-Pac. Entomol. 2011, 14, 11–14. [Google Scholar] [CrossRef]
  27. Cicková, 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]
  28. Sheppard, D.C.; Tomberlin, J.K.; Joyce, J.A.; Kiser, B.C.; Sumner, S.M. Rearing Methods for the Black Soldier Fly (Diptera: Stratiomyidae). J. Med Entomol. 2002, 39, 695–698. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  29. European Commission. Commission Regulation (EU) 2017/893 of 24 May 2017 amending Annexes I and IV to Regulation (EC) No 999/2001 of the European Parliament and of the Council and Annexes X, XIV and XV to Commission Regulation (EU) No 142/2011 As Regards the Provisions on Processed Animal Protein; Official Journal of the European Union: Aberdeen, UK, 2017. [Google Scholar]
  30. European Commission. Regulation (Ec) No 1069/2009 of The European Parliament AND OF The Council Laying Down Health Rules as Regards Animal By-Products and Derived Products Not Intended for Human Consumption and Repealing Regulation (EC) No 1774/2002 (Animal By-Products Regulation); Official Journal of the European Union: Aberdeen, UK, 2009. [Google Scholar]
  31. APHA. Import of Processed Animal Protein (PAP) Derived from Farmed Insects Not for Human Consumption from Third Countries. Import Information Note (IIN) ABP/45; The Animal and Plant Health Agency (APHA): Surrey, UK, 2020.
  32. Liu, X.; Chen, X.; Wang, H.; Yang, Q.; Rehman, K.u.; 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]
  33. Wang, C.; Qian, L.; Wang, W.; Wang, T.; Deng, Z.; Yang, F.; Xiong, J.; Feng, W. Exploring the potential of lipids from black soldier fly: New paradigm for biodiesel production (I). Renew. Energy 2017, 111, 749–756. [Google Scholar] [CrossRef]
  34. Gortari, M.C.; Hours, R.A. Biotechnological processes for chitin recovery out of crustacean waste: A mini-review. Electron. J. Biotechnol. 2013, 16, 14. [Google Scholar]
  35. Temple, W.D.; Radley, R.; Baker-French, J.; Richardson, F. Use of Enterra Natural Fertilizer (Black Soldier Fly Larvae Digestate) As a Soil Amendment; Enterra Feed Corporation: Maple Ridge, BC, Canada, 2013; Available online: https://easyasorganics.com.au/wp-content/uploads/2021/02/I-172_Frass_Research_Final-Report.pdf (accessed on 25 July 2021).
  36. Win, S.S.; Ebner, J.H.; Brownell, S.A.; Pagano, S.S.; Cruz-Dilone, P.; Trabold, T.A. Anaerobic digestion of black solider fly larvae (BSFL) biomass as part of an integrated biorefinery. Renew. Energy 2018, 127, 705–712. [Google Scholar] [CrossRef]
  37. Braguglia, C.M.; Gallipoli, A.; Gianico, A.; Pagliaccia, P. Anaerobic bioconversion of food waste into energy: A critical review. Bioresour. Technol. 2018, 248, 37–56. [Google Scholar] [CrossRef]
  38. Zhang, C.; Su, H.; Baeyens, J.; Tan, T. Reviewing the anaerobic digestion of food waste for biogas production. Renew. Sustain. Energy Rev. 2014, 38, 383–392. [Google Scholar] [CrossRef]
  39. WRAP. Why Take Action: Legal/Policy Case. Available online: http://www.wrap.org.uk/content/why-take-action-legalpolicy-case (accessed on 25 July 2021).
  40. Bava, L.; Jucker, C.; Gislon, G.; Lupi, D.; Savoldelli, S.; Zucali, M.; Colombini, S. Rearing of Hermetia illucens on Different Organic By-Products: Influence on Growth, Waste Reduction, and Environmental Impact. Animals 2019, 9, 289. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  41. 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]
  42. Oonincx, D.G.A.B.; Broekhoven, S.v.; 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] [PubMed] [Green Version]
  43. Danieli, P.P.; Lussiana, C.; Gasco, L.; Amici, A.; Ronchi, B. The Effects of Diet Formulation on the Yield, Proximate Composition, and Fatty Acid Profile of the Black Soldier Fly (Hermetia illucens L.) Prepupae Intended for Animal Feed. Animals 2019, 9, 178. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  44. Henderson, R.J. Fatty acid metabolism in freshwater fish with particular reference to polyunsaturated fatty acids. Arch Tierernahr. 1996, 49, 5–22. [Google Scholar] [CrossRef]
  45. Tacon, A.G.J. The Nutrition and Feeding of Farmed Fish and Shrimp–A Training Manual, 1. The Essential Nutrients; Food and Agriculture Organization of The United Nations: Brasilia, Brazil, 1987. [Google Scholar]
  46. Dick, H.; Scholes, P. Comparing the Costs of Alternative Waste Treatment Options; WRAP: Banbury, UK, 2019. [Google Scholar]
  47. Kerby, C.; Vriesekoop, F. An Overview of the Utilisation of Brewery By-Products as Generated by British Craft Breweries. Beverages 2017, 3, 24. [Google Scholar] [CrossRef] [Green Version]
  48. Thiex, N.; Novotny, L.; Crawford, A. Determination of ash in animal feed: AOAC official method 942.05 revisited. J. AOAC Int. 2012, 95, 1392–1397. [Google Scholar] [CrossRef]
  49. NRC. Nutrient Requirements of Fish and Shrimp; Animal Nutrition Series; The National Academies Press: Washington, DC, USA, 2011. [Google Scholar]
  50. Korkmaz, A.S.; Cakirogullari, G.C. Effects of partial replacement of fish meal by dried baker’s yeast (Saccharomyces cerevisiae) on growth performance, feed utilization and digestibility in koi carp (Cyprinus carpio L., 1758) fingerlings. J. Anim. Vet. Adv. 2011, 10, 346–351. [Google Scholar] [CrossRef] [Green Version]
  51. Jucker, C.; Lupi, D.; Moore, C.D.; Leonardi, M.G.; Savoldelli, S. Nutrient Recapture from Insect Farm Waste:Bioconversion with Hermetia illucens (L.) (Diptera: Stratiomyidae). Sustainability 2020, 12, 362. [Google Scholar] [CrossRef] [Green Version]
  52. Kissel, D.E.; Risse, M.; Sonon, L.; Harris, G. Calculating the Fertilizer Value of Broiler Litter; The U.S. Department of Agriculture and Counties of the State Cooperating, The University of Georgia and Fort Valley State University: Fort Valley, GA, USA, 2015.
  53. Penhallegon, R. Nitrogen-Phosphorus-Potassium Values Oforganic Fertilizers; Oregon State University Extension Service: Lane County Office: Eugene, OR, USA, 2003. [Google Scholar]
  54. AHDB. Monthly Average Prices for October 2019 in GB Fertiliser Price Market Update A.a.H.D.B. (AHDB), Editor; Agriculture and Horticulture Development Board (AHDB): Warwickshire, CV8 2TL, UK, 2019; Available online: https://ahdb.org.uk/GB-fertiliser-prices (accessed on 25 July 2021).
  55. Tschirner, M.; Simon, A. Influence of different growing substrates and processing on the nutrient composition of black soldier fly larvae destined for animal feed. J. Insects Food Feed 2015, 1, 249–259. [Google Scholar] [CrossRef]
  56. Wilson, R.P. Protein and amino acids. In Fish Nutrition, 3rd ed.; Halver, J.E., Hardy, R.W., Eds.; Elsevier Science: San Diego, CA, USA, 2002; pp. 144–179. [Google Scholar]
  57. Miles, R.D.; Chapman, F.A. The Benefits of Fish Meal in Aquaculture Diets; Place, N.T., Ed.; The Fisheries and Aquatic Sciences Department, U.S. Department of Agriculture, UF/IFAS Extension, University of Florida: Gainesville, FL, USA, 2018.
  58. INRA-CIRAD-AFZ. Fish Meal, Protein 65%. INRA-CIRAD-AFZ Feed Tables 2020. Available online: https://www.feedtables.com/content/fish-meal-protein-65 (accessed on 10 April 2020).
  59. Bhat, T.H.; Balkhi, M.H.; Banday, T. Use of soybean products in aquafeeds: A review. In Soybean in Aquaculture; University of Agricultural Sciences and Technology of Kashmir: Srinagar, India, 2012. [Google Scholar]
  60. Hasan, A.; Tan, J. The Current State of Plant-Based Proteins in Aquaculture Feed; Biomin: Getzersdorf, Austria, 2020; Available online: https://www.biomin.net/science-hub/the-current-state-of-plant-based-proteins-in-aquaculture-feed/ (accessed on 25 July 2021).
  61. Cremer, M.C. Use and Future Prospects for Use of Soy Products in Aquaculture; USSEC-U.S. Soybean Export Council: Singapore, 2019; Available online: https://ussec.org/resources/future-prospects-soy-products-aquaculture/ (accessed on 25 July 2021).
  62. Heuzé, V.; Tran, G.; Kaushik, S. Soybean Meal. Feedipedia 4 March. Available online: http://www.feedipedia.org/node/674 (accessed on 10 April 2020).
  63. Dayrit, F.M. The Properties of Lauric Acid and Their Significance in Coconut Oil. J. Am. Oil Chem. Soc. 2015, 92, 1–15. [Google Scholar] [CrossRef]
  64. Kabara, J.J.; Swieczkowski, D.M.; Conley, A.J.; Truant, J.P. Fatty Acids and Derivatives as Antimicrobial Agents. Antimicrob. Agents Chemother. 1972, 2, 23–28. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  65. Walters, D.R.; Walker, R.L.; Walker, K.C. Lauric Acid Exhibits Antifungal Activity Against Plant Pathogenic Fungi. J. Phytopathol. 2003, 151, 228–230. [Google Scholar] [CrossRef]
  66. Zeiger, K.; Popp, J.; Becker, A.; Hankel, J.; Visscher, C.; Klein, G.; Meemken, D. Lauric acid as feed additive–An approach to reducing Campylobacter spp. in broiler meat. PLoS ONE 2017, 12, e0175693. [Google Scholar] [CrossRef] [Green Version]
  67. Hayes, D.G. Fatty Acids Based Surfactants and Their Uses. In Fatty Acids, Chemistry, Synthesis, and Applications; Ahmad, M.U., Ed.; Academic Press and AOCS Press: Cambridge, MA, USA, 2017; pp. 355–384. [Google Scholar]
  68. McNaught, A.D.; Wilkinson, A. Compendium of Chemical Terminology, (the “Gold Book”), 2nd ed.; Chalk., S.J., Ed.; Blackwell Scientific Publications: Oxford, UK, 1997. [Google Scholar]
  69. Kelm, G.R.; Wickett, R.R. The Role of Fatty Acids in Cosmetic Technology. In Fatty Acids, Chemistry, Synthesis, and Applications; Ahmad, M.U., Ed.; Academic Press and AOCS Press: Cambridge, MA, USA, 2017; pp. 385–404. [Google Scholar]
  70. Huang, C.B.; George, B.; Ebersole, J.L. Antimicrobial activity of n-6, n-7 and n-9 fatty acids and their esters for oral microorganisms. Arch. Oral Biol. 2010, 55, 555–560. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  71. Ecothrive. Ecothrive Charge, Soil Conditioner and Biostimulant. 2020. Available online: https://www.ecothrive.co.uk/catalogue/charge_6/ (accessed on 25 July 2021).
  72. Schmitt, E.; de Vries, W. Potential benefits of using Hermetia illucens frass as a soil amendment on food production and for environmental impact reduction. Curr. Opin. Green Sustain. Chem. 2020, 25, 100335. [Google Scholar]
Table 1. Pre-consumer and manufacturing organic waste streams identified for study.
Table 1. Pre-consumer and manufacturing organic waste streams identified for study.
Organic WasteSourceReason Waste Was Chosen for InvestigationWaste Category and Disposal MethodMedian Gate Fezzze (GBP/tonne) [46]
Fish trimmingsCollected from local fish mongerWaste generated at fish processing facilities. Seeking to track long chain fatty acids in BSFL.Fallen stock and digestive tracks—category II. Parts of stock unconsumed—category III.Material recovery facilities (MRFs): all wastes, GBP 25, contracts from 2018 are GBP 35.
In vessel composting (IVC): mixed food and green, GBP 50; all feedstock types, GBP 46.
AD: all gates fees, GBP 27.
Energy recovery: GBP 89.
Landfill: non-hazardous waste, including landfill tax (standard rate for 2017/18 is GBP 88.95/tonne), GBP 113.
Sugar beet pulpBritish sugarHighly produced by sugar industry and meat-free.Covered under fruit and vegetable waste.
Bakery wasteLocal bakeryAvailable in high volumes due to short shelf life and meat freeNon-animal by-product approved, depackaged and shred.
Fruit and vegetable wasteHousehold waste (representative of supermarket waste)Available in high volumes and meat-freeNon-animal by-product approved, depackaged and shred.
Cheese wasteHarvey & Brockless (H&B) Cheese in LondonAvailable in high volumes, meat-free and high in fat. Investigating how BSFL respond to high fat material.Covered under dairy products. Treated as bakery and fruit and vegetable, depackaged and shred.
Industrial fish feed wasteSkretting feed manufacturing facilityBy product of aquaculture feed industryAs for fish trimmings.
Brewer’s grains and yeastFirebird BreweryAvailable in high volumes from brewing industry and meat-free.Often used as animal feed or disposed via landfill [47].
Table 2. Substrate reduction alongside growth and performance of BSFL when raised on the identified organic feedstocks.
Table 2. Substrate reduction alongside growth and performance of BSFL when raised on the identified organic feedstocks.
DietFeed Conversion Rate (FCR)Specific Growth Rate (SGR)Larval Growth Rate (LGR) (mg/day)Efficiency of Conversion of the Ingested Food (ECI)Waste Reduction Index (WRI) (g/day)Substrate Reduction (SR) (%)
Fish trimmings5.98 ± 2.77 ac16.92 ± 3.36 a9.25 ± 4.94 a0.32 ± 0.08 a28.17 ± 5.26 ad −54.49 ± 8.59 a
Sugar beet pulp20.54 ± 8.68 b9.95 ± 1.84 b2.19 ± 0.54 b0.11 ± 0.04 b14.79 ± 0.68 b −60.98 ± 8.31 ac
Bakery waste4.84 ± 1.45 a17.66 ± 1.68 a9 ± 2.83 a0.35 ± 0.08 a22.66 ± 1.26 ae −70.26 ± 9.49 bc
Fruit and vegetable waste7.97 ± 1.1 ac16.08 ± 1.21 a6.45 ± 0.79 ac0.15 ± 0.01 b28.02 ± 2.21 ad −79.28 ± 6.18 b
Cheese waste12.92 ± 2.06 c9.55 ± 0.99 b2.71 ± 0.19 c0.11 ± 0.03 b45.17 ± 4.98 c −63.86 ± 5.63 ac
Fish feed waste6.42 ± 1.25 ac17.39 ± 1.43 a16.05 ± 1.9 d0.55 ± 0.07 c31 ± 1.42 d −37.27 ± 5.4 d
Brewer’s grain and yeast6.78 ± 1.12 ac16.59 ± 1.19 a6.99 ± 0.38 ac0.31 ± 0.04 a21.19 ± 3.32 be −52.04 ± 5.02 a
LGR, ECI, WRI and SR were calculated on a DM basis. Organic materials which do not share a common letter in each column are significantly different p < 0.05.
Table 3. (a) Nutritional profile of waste stream feed materials, proximate. (b) Fatty acid profiles of organic waste stream feed materials.
Table 3. (a) Nutritional profile of waste stream feed materials, proximate. (b) Fatty acid profiles of organic waste stream feed materials.
(a)
ParameterFish TrimmingsSugar Beet PulpBakery WasteFruit and Vegetable WasteCheese WasteFish Feed WasteBrewer’s Grains and Yeast
Dry matter (DM) (%)31.0752.6558.6312.4753.5493.9321.66
Crude protein (g/100 g DM)42.428.6218.228.4231.7154.0249.95
Crude fat (g/100 g DM)36.470.362.661.6857.2710.406.56
Fibre (g/100 g DM)0.004.210.650.100.221.630.88
Ash (g/100 g DM)5.224.221.970.663.356.511.03
Energy (MJ/kg)7.58.4711.112.0216.3320.894.41
(b)
Fatty Acids (g/100 g DM)Fish TrimmingsSugar Beet PulpBakery WasteFruit and Vegetable WasteCheese WasteFish Feed WasteBrewer’s Grains and Yeast
Caproic acidC6:01.60.00.10.16.40.30.1
Caprylic acidC8:00.010.010.010.000.310.010.00
Capric acidC10:00.000.000.000.000.760.000.00
Undecanoic acidC11:00.000.000.000.000.180.000.00
Lauric acidC12:00.020.010.010.001.020.020.01
Tridecanoic acidC13:03.030.050.770.550.881.463.06
Myristic acidC14:00.950.010.010.013.740.630.01
Myristoleic acidC14:1n-50.030.000.000.010.640.010.00
Pentadecanoic acidC15:00.080.000.000.000.410.040.00
cis-10 pentadecanoic acidC15:10.650.000.110.090.290.400.31
Palmitic acidC16:02.620.080.290.0510.751.550.35
Palmitoleic acidC16:1n-70.710.000.000.000.740.420.01
cis-10 heptadecanoic acidC17:10.030.000.000.000.030.010.01
Stearic acidC18:00.500.020.040.013.450.280.03
Elaidic acid, Oleic acidC18:1n-92.700.030.620.037.572.490.22
Linoleic acidC18:2n-60.950.030.450.070.541.380.66
α-linolenic acidC18:3n-30.200.000.060.010.160.380.07
Gamma-linolenic acid (GLA)C18:3n-60.010.000.000.000.010.010.00
Arachidic acidC20:00.040.000.010.000.060.050.00
Gondoic acidC20:1n-94.420.000.030.000.030.980.07
Eicosadienoic acidC20:2n-60.120.000.010.000.020.050.00
cis-11,14,17 eicosatrienoic acidC20:3n-30.120.000.000.000.000.030.00
cis-8,11,14 eicosatrienoic acidC20:3n-60.030.000.000.000.030.010.01
Arachidonic acidC20:4n-60.030.000.000.000.030.040.00
Eicosapentaenoic acid (EPA)C20:5n-30.240.000.000.000.010.560.01
Heneicosanoic acidC21:00.020.000.000.000.030.010.03
Behenic acidC22:00.020.000.000.000.040.060.01
Erucic acidC22:1n-90.580.000.010.000.010.120.01
cis-13,16-docosadienoic acidC22:20.070.000.000.000.020.010.01
Docosahexaenoic acid (DHA)C22:6n-30.220.000.000.000.000.610.00
tricosanoic acidC23:00.010.000.000.000.020.000.00
lignoceric acidC24:00.030.000.000.010.030.010.01
nervonic acidC24:10.600.000.000.000.000.080.01
Sum Sat FA8.950.231.230.7728.124.433.66
Sum unsaturated FA11.730.061.300.2210.137.561.39
Sum monoenes9.730.030.780.149.304.500.64
Sum n-6 FA1.140.030.460.070.631.480.68
Sum n-3 FA0.790.000.060.010.171.570.07
Unsat/Saturated1.310.281.060.290.361.710.38
n-6/n-31.4413.477.176.093.660.949.29
n-3/n-60.690.070.140.160.271.060.11
Table 4. (a) Nutritional profiles of BSFL meals, proximate and amino acid analysis. (b) Nutritional profiles of BSFL meals, fatty acid analysis.
Table 4. (a) Nutritional profiles of BSFL meals, proximate and amino acid analysis. (b) Nutritional profiles of BSFL meals, fatty acid analysis.
(a)
Parameter (g/100 g DM)BSFL Meals
Fish TrimmingsSugar Beet PulpBakery WasteFruit and Vegetable WasteCheese WasteFish Feed WasteBrewer’s Grains and Yeast
ProximateCrude protein46.6243.1543.0736.0343.1845.7051.05
Crude fat35.0535.4937.6340.3036.9435.2227.00
Amino acids
EssentialArginine2.061.791.841.431.952.141.96
Histidine1.431.341.311.011.301.441.34
Isoleucine1.971.841.761.451.821.992.11
Leucine3.853.582.792.282.853.153.30
Lysine2.412.192.411.972.382.533.15
Methionine0.870.780.790.630.820.800.85
Cystine0.290.270.330.290.230.220.37
Phenylalanine1.731.691.811.511.852.052.44
Tyrosine2.031.911.961.485.285.735.44
Threonine1.681.561.611.281.641.801.92
Valine2.672.522.622.112.642.913.04
Non-essentialAlanine2.942.922.812.362.762.914.46
Aspartic acid3.863.763.893.103.694.124.05
Glutamic acid4.474.264.373.484.404.405.13
Glycine2.592.352.351.842.372.612.65
Proline2.652.472.321.912.882.973.35
Serine1.831.731.701.331.691.831.94
Sum of AA39.3136.9536.6829.4740.5643.6147.51
Tryptophan was not tested for.
(b)
Parameter (g/100 g DM)BSFL Meals
Fish TrimmingsSugar Beet PulpBakery WasteFruit and Vegetable WasteCheese WasteFish Feed WasteBrewer’s Grains and Yeast
Fatty acids
Caprylic acidC8:0<LOD<LOD<LOD<LOD0.01<LOD<LOD
Capric acidC10:00.340.350.340.280.370.480.23
Lauric acidC12:012.5920.3719.8015.3912.3516.717.18
Myristic acidC14:02.333.693.883.393.592.971.83
Myristelaidic acidC14:1n-50.060.090.080.280.310.080.06
Pentadecanoic acidC15:00.13<LOD0.040.080.220.060.08
Palmitic acidC16:04.714.294.745.727.393.614.60
Palmitoleic acidC16:1n-72.230.971.052.061.801.181.34
C16:2n-60.04<LOD<LOD<LOD<LOD0.02<LOD
Stearic acidC18:00.550.550.680.730.950.440.69
C18:1n-5<LOD<LOD<LOD<LOD<LOD0.020.01
Elaidic acid, Oleic acidC18:1n-95.563.023.998.876.684.134.23
cis-vaccenic acidC18:1n-70.42<LOD0.110.120.230.260.38
C18:2n-4<LOD<LOD<LOD<LOD0.040.01<LOD
Linoleic acidC18:2n-62.291.282.111.651.272.003.57
α-linolenic acidC18:3n-30.330.180.300.360.230.280.42
Gamma-linolenic acid (GLA)C18:3n-60.03<LOD<LOD<LOD0.020.010.01
Stearidonic acid (SDA)C18:4n-30.23<LOD<LOD<LOD0.010.220.17
Arachidic acidC20:0<LOD0.04<LOD<LOD0.030.030.06
C20:1n-80.09<LOD<LOD<LOD<LOD0.240.20
Gadoleic acidC20:1n-110.44<LOD<LOD<LOD0.110.340.30
Eicosadienoic acidC20:2n-6<LOD<LOD<LOD<LOD0.070.070.06
Arachidonic acidC20:4n-60.14<LOD<LOD0.040.050.030.02
Eicosapentaenoic acid (EPA)C20:5n-31.200.090.040.080.180.780.53
Behenic acidC22:0<LOD<LOD<LOD<LOD0.030.020.04
Cetoleic acidC22:1n-11<LOD<LOD<LOD<LOD<LOD0.120.07
Docosahexaenoic acid (DHA)C22:6n-30.32<LOD<LOD<LOD<LOD0.060.07
Sum Sat FA20.6429.2829.4725.5924.9324.3314.70
Sum unsaturated FA13.375.647.6813.4610.999.8511.43
Sum monoenes8.794.085.2311.329.126.386.58
Sum n-6 FA2.501.282.111.691.412.133.66
Sum n-3 FA2.080.270.340.440.421.341.20
Unsat/Saturated0.650.190.260.530.440.400.78
n-6/n-31.204.706.223.823.351.593.06
n-3/n-60.830.210.160.260.300.630.33
Unknown2.951.610.91.42.742.933.24
<LOD = below level of detection. Essential fatty acids highlighted in bold.
Table 5. Apparent bioconcentration factor (aBCF) of nutritional parameters tested for and present in both feed materials and BSFL meals, achieved by BSFL during production feeding on each waste stream material.
Table 5. Apparent bioconcentration factor (aBCF) of nutritional parameters tested for and present in both feed materials and BSFL meals, achieved by BSFL during production feeding on each waste stream material.
Parameter (%DM)BSFL Apparent Bioconcentration Factor (aBCF)
Fish TrimmingsSugar Beet PulpBakery WasteFruit and Vegetable WasteCheese WasteFish Feed WasteBrewer’s Grains and Yeast
Crude protein1.15.02.44.31.40.81.0
Crude fat1.098.414.123.90.63.44.1
Fatty acids
Caprylic acidC8:000000.100
Capric acidC10:0216.4043.46.40.757.40
Lauric acidC12:0561.921.1114.6157.918.8230.2329.0
Myristic acidC14:02.64.929.115.21.51.457.2
Pentadecanoic acidC15:01.701.42.70.80.48.2
Palmitic acidC16:01.90.51.14.71.10.73.1
Palmitoleic acidC16:1n-73.39.217.742.53.80.864.2
Stearic acidC18:01.10.31.12.10.40.55.5
Elaidic acid, Oleic acidC18:1n-92.11.10.510.61.40.54.6
Linoleic acidC18:2n-62.50.50.31.03.60.41.3
α-linolenic acidC18:3n-31.70.90.31.32.30.21.6
Gamma-linolenic acid (GLA)C18:3n-62.40004.80.20
Arachidic acidC20:00.00.4000.70.23.1
Eicosadienoic acidC20:2n-60.00005.20.53.0
Arachidonic acidC20:4n-64.7002.62.50.34.7
Eicosapentaenoic acid (EPA)C20:5n-35.104.914.119.80.419.7
Behenic acidC22:000001.30.12.0
Docosahexaenoic acid (DHA)C22:6n-31.500000.00
Sum Sat FA2.41.31.71.41.41.61.0
Sum unsaturated FA1.20.90.42.51.70.42.0
Sum monoenes0.91.20.53.41.50.42.5
Sum n-6 FA2.30.50.31.03.50.41.3
Sum n-3 FA2.71.40.41.63.80.34.0
Table 6. Comparison of BSFL frass NPK values with other manure fertilizers [53].
Table 6. Comparison of BSFL frass NPK values with other manure fertilizers [53].
FertiliserNitrogen (N) %Phosphorus (P) %Potassium (K) %
BSFL frass4.92.61.7
Cow manure0.5–20.2–0.70.4–2
Horse manure0.7–1.50.2–0.70.6–0.8
Pig manure0.4–20.5–10.4–1.2
Poultry manure1.5–61–40.5–3
Sheep manure2.2–3.60.3–0.60.7–1.7
Rabbit manure3–4.81.5–2.81–1.3
Table 7. Cost of each nutrient (N, P and K) based on other fertiliser prices.
Table 7. Cost of each nutrient (N, P and K) based on other fertiliser prices.
FertiliserCost (GBP/Tonne)Kg of Nutrient Per TonneCost of Nutrient (GBP/Tonne)Average Cost of Nutrient (GBP/kg)
Ammonium nitrite (34.5% N)2583450.750.67
Granular Urea-standard specification (46% N)2724600.59
Muriate of Potash (MOP) (60% K20)2836000.470.47
Diammonium Phosphate (DAP) (46% P2O5)3504600.760.71
Triple Super Phosphate (TSP) (46% P2O5)3024600.66
Prices correct as of October 2019 [54].
Table 8. Estimated value of BSFL frass compared to other manure fertilisers based on midpoint NPK content, taken from Table 5, and value of nutrients, taken from Table 6.
Table 8. Estimated value of BSFL frass compared to other manure fertilisers based on midpoint NPK content, taken from Table 5, and value of nutrients, taken from Table 6.
FertiliserCost of Nutrient (GBP/Tonne)Total Cost (GBP/Tonne)
Nitrogen (N)Phosphorus (P)Potassium (K)
BSFL frass32.812.212.157.1
Cow manure8.42.18.519.0
Horse manure7.42.15.014.5
Pig manure8.03.55.717.2
Poultry manure25.111.812.449.3
Sheep manure19.42.18.530.1
Rabbit manure26.110.18.244.4
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Magee, K.; Halstead, J.; Small, R.; Young, I. Valorisation of Organic Waste By-Products Using Black Soldier Fly (Hermetia illucens) as a Bio-Convertor. Sustainability 2021, 13, 8345. https://0-doi-org.brum.beds.ac.uk/10.3390/su13158345

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Magee K, Halstead J, Small R, Young I. Valorisation of Organic Waste By-Products Using Black Soldier Fly (Hermetia illucens) as a Bio-Convertor. Sustainability. 2021; 13(15):8345. https://0-doi-org.brum.beds.ac.uk/10.3390/su13158345

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Magee, Kieran, Joe Halstead, Richard Small, and Iain Young. 2021. "Valorisation of Organic Waste By-Products Using Black Soldier Fly (Hermetia illucens) as a Bio-Convertor" Sustainability 13, no. 15: 8345. https://0-doi-org.brum.beds.ac.uk/10.3390/su13158345

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