Next Article in Journal
New Insights in Lifetime Migrations of Albacore Tuna (Thunnus alalunga, Bonnaterre, 1788) between the Southwest Indian and the Southeast Atlantic Oceans Using Otolith Microchemistry
Next Article in Special Issue
Administration of Red Macroalgae (Galaxaura oblongata) in the Diet of the Rainbow Trout (Oncorhynchus mykiss) Improved Immunity and Hepatic Gene Expression
Previous Article in Journal
Effects of Cold Stress on the Hemolymph of the Pacific White Shrimp Penaeus vannamei
Previous Article in Special Issue
The Effects of Grapevine (Vitis vinifera L.) Leaf Extract on Growth Performance, Antioxidant Status, and Immunity of Zebrafish (Danio rerio)
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

The Impact of Marine Resource-Free Diets on Quality Attributes of Atlantic Salmon

1
Aqua Cognoscenti LLC., 479 Henslowe Lane, West Columbia, SC 29170, USA
2
Anthropocene Institute, 855 El Camino Real, Ste 13A N399, Palo Alto, CA 94301, USA
3
Food Science and Technology, Virginia Tech, Blacksburg, VA 24061, USA
4
School for the Environment, University of Massachusetts Boston, Boston, MA 02125, USA
5
Aquatic Feed Technologies LLC., 48 West Plaza del Lago, Islamorada, FL 33036, USA
*
Authors to whom correspondence should be addressed.
Fishes 2024, 9(1), 37; https://doi.org/10.3390/fishes9010037
Submission received: 20 December 2023 / Revised: 14 January 2024 / Accepted: 15 January 2024 / Published: 17 January 2024
(This article belongs to the Special Issue Fish Nutrition and Feed Technology II)

Abstract

:
The influence of feeding Atlantic salmon for 90 days on diets that excluded fishmeal (FM) and fish oil (FO) was examined for influence on various quality traits. In addition, the effect of adding krill meal (KM; 0%, 2.5%, and 5%), as a putative feed palatant was also examined. Total replacement of FM/FO had a limited effect on production characteristics, affecting percentage yields of headed and gutted control fish and their standard length (p < 0.05). Variances between dietary groups were observed for pigmentation, and plant protein-based KM-free-fed fish returned deeper hues across their belly, NQC (Norwegian Quality Cut), and back portions (p < 0.03). No differences were measured for relative fin condition. δ13C and δ15N concentrations were lower and higher, respectively (p < 0.05) for fish fed the FM/FO-based diet. δ13C:δ15N likewise differed between treatments with FM/FO-fed salmon expressing higher ratios. Fillet mechanical characteristics varied with fish fed on animal protein-based diets, without KM expressing higher springiness and resilience (p < 0.05). Fish fed plant-based diets were generally preferred by younger taste testers. The results from this trial illustrate that FM/FO can be completely removed from salmon diets without problematic effects on quality and palatability attributes.
Key Contribution: Complete elimination of FM/FO from the diet of Atlantic salmon post-smolts and their replacements with alternative animal or plant proteins, combined with algal oil, had no effect on growth. The fillet color was of a deeper hue in fish fed the all-plant protein diet. Both the use of fillet stable isotope concentration (δ13C and δ15N) and their ratios did not permit distinction between fish fed FM/FO-based diets and those fed FM/FO-free, KM-containing feeds. Complete replacement of FM/FO from Atlantic salmon feeds had little effect on fillet texture or organoleptic profiles.

1. Introduction

The use of fishmeal (FM) and fish oil (FO) in salmon feeds has declined markedly over the last two decades and this trend is predicted to continue [1]. The reduction in FM/FO has been facilitated, to a certain extent, by an improved understanding of salmon nutrition, genetic selection, advances in feed technologies, and innovation in feed delivery methods [2,3,4,5]. Other attributes driving the reduction in the use of FM/FO have been the rising price of both commodities in the international marketplace [6] and the emergence of a more refined and opinionated consumer. Prices for FM/FO have risen as competition for both resources has increased while availability has generally weakened. Reduced catches of forage fish, which provide the raw material for the production of FM/FO, have emerged due to over-fishing, natural and climate-induced effects (e.g., El Niño–Southern Oscillation, the Madden–Julian Oscillation), and the increased consumption of forage fish resources by society [7,8,9,10]. Another concern that has forced the aquafeed sector to reduce its reliance on FM/FO is public awareness of the negative direct and indirect effects of forage fisheries on marine and coastal ecosystems [11]. Consumers are now more mindful of issues surrounding sustainability, including losses to biodiversity such as the consequences of intense fishing operations on populations of marine mammals, seabirds, and reptiles [12,13,14]. Put plainly, nowadays consumers insist that food production systems are safe, ethically, and environmentally reactive and follow the principles of the circular economy with zero discard, combined with more rigorous criteria for animal health and welfare.
In response to the above and other issues, aquafeed manufacturers and researchers have continued to examine the prospect of further reducing or eliminating FM/FO from Atlantic salmon feeds. While this has met with varying degrees of success, the most satisfactory responses have been gained using animal protein-based diets and those comprising blends of plant protein concentrates, and their combinations cf. [15,16,17,18,19,20,21,22,23]. Indeed, some longer-term studies support the concept that, with judicious selection and blending of various alternative proteins and oils, it may prove possible to completely replace FM/FO in salmon feeds [24,25,26,27,28,29,30]. Due to the potential savings inherent in employing FM/FO alternatives, even given poorer Feed Conversion Ratios (FCRs) and reduced growth rates, profit margins can increase [31,32,33] while simultaneously addressing some consumer concerns. In fact, previous studies reveal that shoppers will pay higher prices for salmon produced under sustainable conditions, provided account is taken of fish welfare, and that food safety is guaranteed [34,35,36]. For example, consumers are prepared to pay a 25.3% premium for organic salmon in the UK [37], 20% in Denmark [38], 15% in Norway [39], 11–20% in Croatia [40], and an 11% premium in France [41].
Comparatively few studies have evaluated the quality attributes of Atlantic salmon fed on completely marine resource-free feeds. Most reports have evaluated fish fed diets that substitute either FM or FO rather than excluding both ingredients simultaneously [24,42,43,44,45,46,47]. Since refined consumers will not accept sub-standard foodstuffs, there is a need to determine whether concurrent FM/FO replacement negatively influences the overall quality of farmed Atlantic salmon. Accordingly, we examined the impact of feeding post-smolt Atlantic salmon with various diets over a 90-day period and assessed the impact of each on the mechanical and organoleptic/palatability characteristics of resultant fillets. Fillet color characteristics were examined as a quality indicator and fin and eye condition indices were assessed to determine whether the marine resource-free diets influenced overall animal welfare. In addition, we explored the value of uncovering carbon and nitrogen isotope ratios as a means of confirming the marine resource-free nature of feeds.

2. Materials and Methods

2.1. Raw Material

The fish employed in the present study were derived from a 90-day growth trial which was undertaken to assess the response of Atlantic salmon to dietary krill meal (KM) inclusion. The results of these experiments, which evaluated seven diets, have been presented previously [6], and this study is a further examination of morphological, functional, and consumer acceptance attributes of the fish that were not originally addressed. Four fish were randomly taken from four replicated tanks for each of the seven diets, which comprised a control FM/FO-based feed (C1), plant-based feeds incorporating 0% (P1), 2.5% (P2), and 5% (P3) KM, and animal-based formulas that incorporated 0% (A1), 2.5% (A2), and 5% (A3) KM (n = 16 fish per dietary treatment). The main protein source in the animal-based feeds was poultry meal while that of the plant-based feed was soy protein concentrate. Both animal and plant-based feeds incorporated Schizochytrium sp. and canola oils while the control feed contained FO only. Since each tank accommodated 45 individuals (180 fish per treatment), the sample size represented ~9% of the original trial’s total population. Fish used for image acquisition (n = 8 per dietary treatment) were sacrificed using an overdose of benzocaine (100 mg L−1) and photographed from the left side using a Canon EOS T7i + 18–55 mm lens. Photographs were taken under fluorescent light and each image incorporated a 30 cm divided ruler. Acquired images were rasterized in Photoshop 2022 (Adobe Systems Inc., San Jose, CA USA) and employed for determining the presence of cataracts and degree of fin erosions. Salmon used for filleting, textural analyses, and assessment of δ13C: δ15N ratios were fasted for 48 h to avoid fecal contamination, immobilized in ice, and bled by severance of the gill arches (n = 8 per dietary treatment). Since there is the potential for significant processor variation in fillet yields, filleting was carried out by one individual to minimize this possibility.

2.2. Assessment of Surface Area, Eyes and Fins

Body surface area (BSA) was approximated as a function of mass using the formula (13.9 W0.61), as determined by [48].
BSA = 13.9 × W0.61
All fish images were evaluated for the presence of cataracts (n = 8 per diet) using a 0–4 scale as described in [49]. The dorsal fin was employed to evaluate fin erosion (n = 8 per diet) and was selected since this appendage is one of the most sensitive nociceptive zones [50]. Fin erosion was quantified using a modification of the relative fin index (RFI) as described in [51]:
RFI = ( fin   length × 100 ) standard   length
Standard length (SL) was used in preference to total length to avoid measurement inaccuracies due to caudal fin fraying. Dorsal fin height was measured from the point of insertion of the anterior-most fin ray to its tip. The degree of erosion (fraying, splitting, abrasion, and other forms of deterioration; Figure 1) was assessed using a 5-point ordinal scale adapted from MacLean et al. [51]. A 0 score indicated 0–10% fin erosion representing good condition; 1, 10–20% loss demonstrating moderate condition; 2, 20–30% erosion characterizing moderate damage; 3, 30–60% being indicative of severe damage; and 4, >60% erosion, signifying extensive damage (Figure 1). The overall external condition of each fish was examined visually.

2.3. Texture and Color Determination

Sample preparation: Frozen fillets were thawed in the refrigerator (<4 °C) for 24 h. Samples were then brought to room temperature (20 °C) over a two-hour period prior to texture analysis. This ensured that all samples were analyzed at the same temperature and were verified by a thermometer. Raw salmon fillets (3 fillets per tank, 28 tanks) from each treatment group underwent texture profile analysis (TPA) using a TA.XT Plus Texture Analyzer outfitted with a spherical TA-18 Probe (Texture Technologies Corp., Hamilton, MA, USA). Measurements were taken two times along the lateral line (anterior and posterior) for each fillet and subsequently averaged. The TPA method employed to determine hardness, springiness, resilience, and cohesiveness was adapted from [53]. Fillet color was visually assessed using a DSM SalmoFan™ Lineal. Inter-observer differences in color determination were avoided by using one individual only.

2.4. Sensory Evaluation

A taste trial was undertaken using fillets derived from each of the experimental and control dietary groups. Thirty-four untrained active consumers of Atlantic salmon were sent blind samples to prepare by baking at 80 °C for 15 min. Each was then asked to establish whether there were differences in the following four main characteristics: odor, flavor, texture, and visual appearance. Within each characteristic, a subset of descriptors was applied, encompassing, odor: sweet odor, off-odor; flavor: sweet flavor, off-flavor, fresh oily flavor; texture: dryness, fiberness, juiciness, softness, chewing residue; and appearance: dry, protein stains, discoloration. After sample evaluation, each panelist was requested to select their favored fillet(s). When several people gathered for the test, each received the identical part of the different fillets to inspect. Ethnicity, gender identity, and age grouping of participants are summarized in Table 1.

2.5. Authenticity of Fillets

Finally, the muscle (taken dorsal to the lateral line, between the second dorsal and caudal fins) of three fish per treatment were also sampled for carbon and nitrogen isotope ratios, as well as strontium analysis. Samples were collected and sent to the Marine Biological Laboratory, Woods Hole, MA, Stable Isotope Laboratory, where they were dried, pulverized, and analyzed for δ15N and δ13C using a Europa 20-20 continuous-flow isotope ratio mass spectrometer interfaced with a Europa ANCA-SL elemental analyzer. The analytical precision based on replicate analyses of isotopically homogeneous international standards is +/− 0.1‰ for both δ15N and δ13C measurements, and about 1% relative to the % N and % C measurements.

2.6. Statistical Analyses

All statistical analyses were performed using JASP software (JASP Team, 2019, Version 0.11.1) at the α = 0.05 level of significance. Differences between treatment means were examined by one-way ANOVA and significant differences were isolated using Tukey’s studentized range (honestly significant difference) test. Any potential tank effect or associated handling/treatment stress was assumed to be identical for each dietary group.

3. Results

There were no differences in weight, length, or K between dietary groups and this extended to gutted weights, headed-gutted weights, fillet weights and yields, and body surface area (Table 2). Percentage yield did however vary between groups, ranging from 79.88 to 83.00% with lower (p < 0.001) values observed for fish fed experimental diets void of KM and salmon fed the P2 formulation (Table 2). Variances (p < 0.03) between dietary groups were apparent for pigmentation in each of the three tested fillet regions and Student’s paired t-tests revealed that, overall, belly color was lighter than either the NQC or back portions (p < 0.001).
Diet had a significant impact on SL, with fish fed the P1 and A3 diets being shorter than those fed the FM/FO-based diet (Table 3). The relative widths (RFW) and heights (RFH) of the dorsal fins did not differ between groups, varying from 42.44 to 45.69 and from 29.81 to 33.88, respectively, with the relative fin index falling (RFI) in the range of 13.4 to 13.8 (Table 3). The number of frays (#F) and fray widths (FW) of the dorsal fin frays also did not differ between treatments (Table 3). No cataracts were discerned in any of the fish, irrespective of dietary treatment.
Mean fillet stable isotope differences (p < 0.05, Table 4, Figure 2) were apparent between salmon fed on the control, FM/FO-based feeds, and all other samples, with δ13C and δ15N concentrations being lower and higher, respectively. Δ13C levels also varied with diet when considering the experimental feeds, with fish fed the diets containing 5% KM and the 2.5% animal protein formulation returning elevated concentrations when compared to P1, P2, and A1 feeds. There were no differences in readings, however, for measured fillet δ15N levels between experimental diets. Nevertheless, the significant variation observed in fillet δ13C had no overall impact on fillet δ13C: δ15N ratios from experimental feeds, which, as illustrated by Figure 2, were all lower (p < 0.05) than the control fillets.
Table 5 and Table 6 summarize measurements for hardness, cohesiveness, springiness, and resilience of the anterior and posterior halves of the fillets derived from the different dietary treatments, respectively. There were no differences discerned in any measured parameter when comparing the anterior fillets. However, evaluation of springiness and resilience for the posterior half of the fillet revealed a higher value for springiness (p < 0.005) in A1-fed salmon fillets when compared against all others, which returned comparable results (Table 6). Additionally, A1 fillets expressed higher resilience readings than those observed in other experimental diets (p < 0.007). The fillets from the FM/FO-fed fish (C1), however, did not differ in resilience to any of the experimental feeds (Table 6).
The average age of the untrained taste testers was 43.1 ± 16.3 years. Declared preferences for specific fillets were in the following order: P3 > P2 > no preference > A2 = A3 (p > 0.05; Figure 3). Testers of Asian, African, and Latino descent expressed preference only for fish fed plant-based, KM-containing feeds (P2 and P3), whereas Caucasians were apparently less discerning, selecting fillets derived from each dietary group except for the control (C1). Interestingly, taster testers who selected no preference were generally older (66.4 ± 12.1 years) than those who selected the P3 fillets (42.2 ± 4.6 years).

4. Discussion

Seafood consumers generally make purchasing decisions based on safety and quality. Willingness to pay (WTP) for products by more sophisticated buyers, however, may include consideration of a variety of other factors. These include issues that are predominantly aligned to commercial fisheries (e.g., by-catch and at-sea discards, ghost fishing, toxic fisheries subsidies, carbon emissions from fleets, human rights infringements) as well as those that are more affiliated with aquaculture (e.g., animal welfare, environmental degradation, genetic pollution, carbon emissions from feed manufacturers, human rights infringements in production and supply chain sectors) [34,54,55,56,57,58,59,60]. Irrespective of whether a salmon is fished or farmed, however, the first impression a consumer obtains is generally visual. How the salmon presents, therefore, represents a significant element in a purchaser’s decision-making process and WTP for the product.
During cultivation, Atlantic salmon are exposed to various stressors that can influence their overall appearance. For example, eyes can become variably opaque due to the presence of cataracts [61]. This condition, which is generally considered to be irreversible, may be caused by nutritional, environmental, chemical, and infectious insults [62]. During the culture of Atlantic salmon, cataracts and the attending poorer vision can lead to abnormal behavior, reduced feed intake, inferior performance, and lowered survival, which also influences profitability. Sissener et al. [63] observed a 6–14% occurrence of cataracts with post-smolts 3 months following transfer to net pens, while Tröße [64], reported mild cataracts and smaller-sized lenses in Atlantic salmon fed on a substantially plant-based diet for 12 months. She suggested that increased risks for cataracts existed due to the low histidine and N-acetylhistidine content of the plant diet. In the present trial, however, there were no signs of eye opacity or hemorrhaging between treatment groups. Thus, over the duration of the trial, the rearing environment and nutrition were acceptable, an observation identical to that of Sissener et al. [63]. Nonetheless, the possibility of cataract development should be thoroughly examined, especially if FM/FO-free feeds are to be deployed over a full production cycle since it has been suggested that dietary levels of histidine should be 14.4 g kg−1 feed [65], which is higher than used herein.
More obvious than cataracts are external injuries to the skin and fins. High-density holding of Atlantic salmon has been reported to elevate fin erosion [66]. However, in the current study stocking densities were maintained below that which is considered stressful [66,67]. Moreover, there were no signs of skin or opercular damage at trial end, indicating a low level of aggressive interaction within tanks and further evidence that the rearing environment used was appropriate. However, cultured salmonids often suffer from fin erosion—damage to the epidermis, dermis, and fin rays—resulting in fraying, splitting, and changes in histology and fin size [68]. Fin erosion is considered an important welfare issue in fish since caudal, dorsal, and pectoral fins are nociceptive. The causes of fin erosion, which can achieve a prevalence of 60–90%+ [63,69,70,71], appear diverse [68,72,73,74,75] but, unlike fin rot, it is not due to bacterial infection. Nor is fin erosion transmissible, but it may, nonetheless, open fish to secondary bacterial infections. In salmonids, damaged fins can result in downgrading by processors on aesthetic grounds and reduced WTP by consumers [76]. In the present study, fin erosion was noted in approximately 45% of the fish examined with no differences between dietary treatments. Moreover, the average fray width of affected fish was 2.12 mm, with the majority only exhibiting modest levels of erosion. A lower prevalence of fin erosion has been observed by others [77,78], although the latter studies used fish maintained in net pens at stocking densities one-quarter to one-tenth that used during the present trial—differences that may provide partial explanations for the detected variations. Nevertheless, further examination of the causes and mitigation of fin damage is warranted.
Flesh color is another important visual quality characteristic, and, in the marketplace, the pink-red color of salmon not only separates them from other species but represents an indicator of freshness and flavor [79]. Most salmon are sold as fillets, and therefore, color is more apparent than eye or fin attributes. The color of salmon also contributes to a consumers’ general enjoyment and gastronomic delight [80]; a detail that increases a shopper’s WTP for redder fillets [79]. Most studies with Atlantic salmon evaluate production characteristics using much larger fish (4+ kg) than employed here, with the consequence that comparison of morphological relationships and sensory characteristics is problematic. For example, several authors have commented on the relationship between the development of flesh color and fish size, which itself is linked to the duration and quantity of pigmented feed fed, dietary lipid concentration, pigment intensity, type, digestibility, deposition, and retention [81,82,83]. In the current study, the belly regions of examined fillets were lighter than the back or Norwegian Quality Cut (NQC), which corroborates the report of Young et al. [84] and others who examined larger fish. However, herein, the overall intensity of color attained for fish of the size range evaluated was in accord with previous observations [85]. Interestingly, there was a tendency toward a more vivid hue in salmon fed the alternative protein diets when compared to the control group, which contrasts with the observations with salmon and trout, where increased fillet lightness has been reported [86,87,88]. Because alternate lipid sources appear to have no influence on pigmentation [30,31,89], the color differences encountered in the current study are difficult to resolve since the darkest hues, as measured by the SalmoFan™, were from fish fed the plant-based diet void of krill meal. The likeliest explanation for the more pronounced coloration of the alternative protein diets, therefore, was the incorporation of Schizochytrium sp. oil at 4.5% of the diet. The oil from these heterotrophic microalgae, belonging to the order Thraustochytriales, not only provides a source of docosahexaenoic acid (DHA)/eicosapentaenoic acid (EPA) but is also known to contain astaxanthin and other pigments [90].
In the present study, irrespective of the animal’s dietary background, instrumental measurements failed to reveal any differences in texture for anterior fillets. However, some subtle differences were observed in springiness and resilience for one of the posterior fillets. Indeed, herein, overall comparisons of anterior and posterior fillets failed to reveal significant anteroposterior differences within treatments. In contrast, under normal conditions of rearing, using FM/FO-based feeds, Casas et al. [91] reported differences in fillet textural measurements taken at anterior and posterior positions of samples from 3+ kg animals, with posterior sites registering greater hardness but lower cohesiveness and springiness. These anterior-to-posterior differences in muscle characters were recorded earlier by [92,93] and others. The noted divergence between the present and other studies may simply reflect disparities in the age/size of fish examined, the dietary formulations employed, or even the season and method of slaughter used [94]. Indeed, it is difficult to compare the findings from the present study with those of others since most have examined the effect of supplementary ingredients or only partial replacements of FM with alternative proteins, and often with larger fish. Nevertheless, both [95,96] reported increased firmness in salmon flesh fed supplementary glutamate, while [44], using an FM-free diet and similarly sized post-smolts to those used here, observed no effect of diet on shear force. Augmented muscle hardness, gumminess, and chewiness have also been reported for other species in which diets were supplemented with high levels of plant and animal proteins and distiller’s grains [89,97,98] although contrary effects have also been encountered [99,100]. KM has been demonstrated to increase fillet firmness in Atlantic salmon and the impact of poultry and plant-based meals on the mechanical and organoleptic characteristics of fillets has received attention elsewhere [2,44,101].
Quality and sensorial analyses of Atlantic salmon have generally employed the so-called NQC as being a typical sample [46,101]. However, as pointed out previously [102,103,104], the distribution of fat in salmon is not homogenous and this can affect organoleptic qualities and distribution of omega-3 fatty acids along the fillet. Accordingly, Nøstbakken and colleagues [105] suggest that the whole fillet rather than just the NQC be used to obtain an impartial compositional analysis, and here we extended this concept to organoleptic evaluation. Additionally, because a small, trained taste panel could never represent the varied perceptions of a naïve target market [106,107], we elected to use regular consumers of salmon (naïve assessors) for the sensory evaluation. Indeed, many studies have determined a null effect of training over consumer assessments for various foods [108,109,110]. Quality elements generally considered relevant to the judgment of seafood include taste, texture, and appearance, and, for salmonids, [80] indicates that taste and texture are especially significant in revealing consumer preferences for salmonid flesh. It is the triumvirate of taste, odor, and color, however, that has true physiologic importance since these attributes stimulate appetite and gratification. An individual’s perceived quality determinants do, however, differ with age, gender, income, educational attainment, racial origin, culinary heritage, and other factors [111,112,113,114]. The latter may explain differences in preference reported here since the naïve testers were of varied age, gender, ethnicity, and educational attainment, while also being of differing culinary heritage (Caucasian, Afro-American, Hispanic, Asian) and geographic origin.
The methods of cooking employed, including baking, as used in the present study, do not appear to interfere with salmon fillet lipid quality or omega-3 fatty acid dynamics [115,116,117] and, by way of confirmation, Barrows et al. [6] reported that a 75 g serving of fish from the present study, irrespective of dietary treatment, was sufficient to exceed daily intake recommendations for EPA+DHA. The use of algal oil as a replacement for FO was suitable given the study findings. The association of fish size to body fat levels and the relationship between fillet fattiness and sensory quality in Atlantic salmon is well documented [118,119,120,121], but size (this study) and body fat did not vary between treatments [6], implying that neither issue impacted sensorial evaluations. Interestingly, Atlantic salmon fed with non-FM/-containing feed, but with 5% KM (P3), proved preferable to all other treatments, with 42% of the respondents having a positive view. Of the remainder, 21% of the panel expressed a liking of P2-fed fish, 15% had no preference, while fillets derived from A2 and A3 feeds polled 6% and 9%, respectively. Noteworthy was that the ‘no preference’ group was of the greatest mean age whereas the P3 group was younger. This is perhaps not surprising given that a higher prevalence of taste disorder has been described in older people from various geographic regions [122,123,124,125], and also reflects the age skew of the taste testers.
Contemporary consumers demand safer and higher-quality food and, when paying premium prices, insist on increased transparency relating to product identity. For salmon, whole, filleted, and cutlet products are generally easy to recognize. Less straightforward, however, is the determination of provenance and production processes for specific seafoods, such as marine resource-free or organic variations. Indeed, according to the FAO, fish products are among the food products most susceptible to fraud [126]. For this reason, a variety of methods have been examined to authenticate, for example, wild and farmed salmon, adulteration (particularly of processed foodstuffs), organic products, and to determine pigment and element levels in salmon muscle [126,127,128,129,130,131,132,133]. In this regard, stable isotope analyses have proven especially useful [131], and we have previously demonstrated its utility in verifying the marine resource-free status of farmed largemouth bass [133]. In the current trial, however, evaluation of muscle δ13C: δ15N ratios at the trial end did not provide the degree of discrimination previously encountered, for example, with largemouth bass. While there was a clear separation between FM/FO and the alternative plant and animal protein diets, the method was unable to separate fish fed diets supplemented with KM. The reason for this remains obscure but further studies are required to substantiate the suitability of the method as a technique for verifying the fidelity of marine resource-free farmed salmon.

5. Conclusions

Total replacement of FM/FO from Atlantic salmon post-smolts had limited effect on growth, influencing only % yields of headed and gutted fish and their standard length. Fillet color was impacted, however, with plant protein-based diets generally providing better coloration. Both δ13C and δ15N and their ratios were also affected but this result did not allow discrimination of marine resource-free (KM) animals from those devoid of KM. There was limited impact of treatment on texture or organoleptic profiles, although springiness and resilience were both affected in the posterior section of the fillets. Notable, however, was that fish reared using plant-based diets were generally preferred by younger taste testers. This study demonstrates categorically that FM/FO can be completely removed from salmon diets without untoward effects on quality attributes. Future studies must be undertaken in order to optimize dietary formulations and fish performance further.

Author Contributions

Conceptualization, F.T.B.; draft manuscript preparation, E.M.; Resources, K.B.C. and E.M.; Writing—review and editing, F.T.B., D.D.K., M.F.T. and K.B.C.; Project administration, K.B.C. All authors have read and agreed to the published version of the manuscript.

Funding

This research received funding through the Anthropocene Institute.

Institutional Review Board Statement

This study was executed at the Centro Experimental Acuícola, Vitapro Chile, Carretera Austral km 23.8, Quillaipe, Puerto Montt, Chile. The described research complied with all relevant internal (code: CEA-1-C-0522; date: September 2022) and international animal welfare laws, guidelines, and policies.

Informed Consent Statement

Not applicable.

Data Availability Statement

All author-owned experimental data are available on request.

Acknowledgments

The authors express gratitude to the staff of the Centro Experimental Acuícola, Chile for assistance in executing the trial and the Anthropocene Institute for its unwavering support throughout.

Conflicts of Interest

Ewen McLea was employed by the company Aqua Cognoscenti LLC and Frederick T. Barrows was employed by the company Aquatic Feed Technologies LLC. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

References

  1. OECD. OECD Review of Fisheries 2022; OECD Publishing: Paris, France, 2022. [Google Scholar] [CrossRef]
  2. McLean, E. Feed ingredients for sustainable aquaculture. In Reference Module in Food Science; Ferranti, P., Ed.; Sustainable Food Science: A Comprehensive Approach; Elsevier Inc.: Amsterdam, The Netherlands, 2023. [Google Scholar] [CrossRef]
  3. Næve, I.; Korsvoll, S.A.; Santi, N.; Medina, M.; Aunsmo, A. The power of genetics: Past and future contribution of balanced genetic selection to sustainable growth and productivity of the Norwegian Atlantic salmon (Salmo salar) industry. Aquaculture 2022, 553, 738061. [Google Scholar] [CrossRef]
  4. Lekang, O.-I. Feeding equipment and control systems. In Feed and Feeding Practices in Aquaculture; Davis, D.A., Ed.; Woodhead Publishing: Cambridge, MA, USA, 2022; pp. 399–426. [Google Scholar]
  5. Bogomolov, I.S.; Afanasyev, V.A.; Ostrikov, A.N.; Startseva, S.V. The choice of rational modes of vacuum deposition of fatty components in the preparation of feed for valuable fish species. IOP Conf Ser. Earth Environ. Sci. 2022, 1052, 012090. [Google Scholar] [CrossRef]
  6. Barrows, F.T.; Campbell, K.B.; Gaylord, T.G.; Sanchez, R.C.M.; Castillo, S.A.; McLean, E. Influence of Krill Meal on the Performance of post-smolt Atlantic salmon that are fed plant-based and animal-based fishmeal and fish oil-free diets. Fishes 2023, 8, 590. [Google Scholar] [CrossRef]
  7. Doney, S.C.; Ruckelshaus, M.; Duffy, J.E.; Barry, J.P.; Chan, F.; English, C.A.; Galindo, H.M.; Grebmeier, J.M.; Hollowed, A.B.; Knowlton, N.; et al. Climate change impacts on marine ecosystems. Ann. Rev. Mar. Sci. 2012, 5, 11–37. [Google Scholar] [CrossRef] [PubMed]
  8. Pacoureau, N.; Rigby, C.L.; Kyne, P.M.; Sherley, R.B.; Winker, H.; Carlson, J.K.; Fordham, S.V.; Barreto, R.; Fernando, D.; Francis, M.P.; et al. Half a century of global decline in oceanic sharks and rays. Nature 2021, 589, 567–571. [Google Scholar] [CrossRef]
  9. Smith, K.E.; Burrows, M.T.; Hobday, A.J.; King, N.G.; Moore, P.J.; Gupta, A.S.; Thomsen, M.S.; Wernberg, T.; Smale, D.A. Biological impacts of marine heatwaves. Ann. Rev. Mar. Sci. 2023, 15, 119–145. [Google Scholar] [CrossRef] [PubMed]
  10. Zeller, D.; Palomares, M.L.D.; Pauly, D. Global fisheries science documents human impacts on oceans: The Sea Around Us serves civil society in the twenty-first century. Ann. Rev. Mar. Sci. 2023, 15, 147–165. [Google Scholar] [CrossRef]
  11. Georgian, S.; Hameed, S.; Morgan, L.; Amon, D.J.; Sumaila, U.R.; Johns, D.; Ripple, W.J. Scientists’ warning of an imperiled ocean. Biol. Cons. 2022, 272, 109595. [Google Scholar] [CrossRef]
  12. Lewison, R.L.; Crowder, L.B.; Wallace, B.P.; Moore, J.E.; Cox, T.; Zydelis, R.; McDonald, S.; DiMatteo, A.; Dunn, D.C.; Kot, C.Y.; et al. Global patterns of marine mammal, seabird, and sea turtle bycatch reveal taxa-specific and cumulative megafauna hotspots. Proc. Natl. Acad. Sci. USA 2014, 111, 5271–5276. [Google Scholar] [CrossRef]
  13. O’Hara, C.C.; Frazier, M.; Halpern, B.S. At-risk marine biodiversity faces extensive, expanding, and intensifying human impacts. Science 2021, 372, 84–87. [Google Scholar] [CrossRef]
  14. Ramos, J.A.; Pereira, L. (Eds.) Seabird Biodiversity and Human Activities; CRC Press: Boca Raton, FL, USA, 2022; p. 270. [Google Scholar]
  15. Mente, E.; Deguara, S.; Santos, M.B.; Houlihan, D. White muscle free amino acid concentrations following feeding a maize gluten dietary protein in Atlantic salmon (Salmo salar L.). Aquaculture 2003, 225, 133–147. [Google Scholar] [CrossRef]
  16. Espe, M.; Lemme, A.; Petri, A.; El-Mowafi, A. Can Atlantic salmon (Salmo salar) grow on diets devoid of fish meal? Aquaculture 2006, 255, 255–262. [Google Scholar] [CrossRef]
  17. Torstensen, B.; Espe, M.; Sanden, M.; Stubhaug, I.; Waagbø, R.; Hemre, G.-I.; Olsvik, P. Novel production of Atlantic salmon (Salmo salar) protein based on combined replacement of fish meal and fish oil with plant meal and vegetable oil blends. Aquaculture 2008, 285, 193–200. [Google Scholar] [CrossRef]
  18. Øverland, M.; Sørensen, M.; Storebakken, T.; Penn, M.; Krogdahl, Å.; Skrede, A. Pea protein concentrate substituting fish meal or soybean meal in diets for Atlantic salmon (Salmo salar)—Effect on growth performance, nutrient digestibility, carcass composition, gut health, and physical feed quality. Aquaculture 2009, 288, 305–311. [Google Scholar] [CrossRef]
  19. Burr, G.S.; Wolters, W.R.; Barrows, F.T.; Hardy, R.W. Replacing fishmeal with blends of alternative proteins on growth performance of rainbow trout (Oncorhynchus mykiss), and early or late stage juvenile Atlantic salmon (Salmo salar). Aquaculture 2012, 334–337, 110–116. [Google Scholar] [CrossRef]
  20. Davidson, J.; Barrows, F.T.; Kenney, P.B.; Good, C.; Schroyer, K.; Summerfelt, S.T. Effects of feeding a fishmeal-free versus a fishmeal-based diet on post-smolt Atlantic salmon Salmo salar performance, water quality, and waste production in recirculation aquaculture systems. Aquacult. Eng. 2016, 74, 38–51. [Google Scholar] [CrossRef]
  21. Metochis, C.P.; Crampton, V.O.; Ruohonen, K.; El-Mowafi, A.; Bell, J.G.; Adams, A.; Thompson, K.D. Effects of marine protein-, marine oil- and marinefree diets on the growth performance and innate immune responses of Atlantic salmon (Salmo salar, L. ) post-smolts. Aquacult. Res. 2017, 48, 2495–2515. [Google Scholar] [CrossRef]
  22. Egerton, S.; Wan, A.; Murphy, K.; Ahern, G.; Sugrue, I.; Busca, K.; Egan, F.; Muller, J.; Whooley, J.; McGinniyy, P.; et al. Replacing fishmeal with plant protein in Atlantic salmon (Salmo salar) diets by supplementation with fish protein hydrolysate. Sci. Rep. 2020, 10, 4194. [Google Scholar] [CrossRef]
  23. Mikołajczak, Z.; Mazurkiewicz, J.; Rawski, M.; Kierończyk, B.; Józefiak, A.; Świątkiewicz, S.; Józefiak, D. Black soldier fly full-fat meal in Atlantic salmon nutrition—Part B: Effects on growth performance, feed utilization, selected nutriphysiological traits and production sustainability in pre-smolts. Ann. Anim. Sci. 2023, 23, 239–251. [Google Scholar] [CrossRef]
  24. Torstensen, B.E.; Bell, J.G.; Sargent, J.R.; Rosenlund, G.; Henderson, R.J.; Graff, I.E.; Lie, Ø.; Tocher, D.R. Tailoring of Atlantic salmon (Salmo salar L.) flesh lipid composition and sensory quality by replacing fish oil with a vegetable oil blend. J. Agric. Food Chem. 2005, 53, 10166–10178. [Google Scholar] [CrossRef]
  25. Jordal, A.-E.O.; Lie, Ø.; Torstensen, B.E. Complete replacement of dietary fish oil with a vegetable oil blend affect liver lipid and plasma lipoprotein levels in Atlantic salmon (Salmo salar L.). Aquacult. Nutr. 2007, 13, 114–130. [Google Scholar] [CrossRef]
  26. Schmidt, V.; Amaral-Zettler, L.; Davidson, J.; Summerfelt, S.; Good, C. The influence of fishmeal-free diets on microbial communities in Atlantic salmon Salmo salar recirculation aquaculture systems. Appl. Environ. Microbiol. 2016, 82, 4470–4481. [Google Scholar] [CrossRef] [PubMed]
  27. Belghit, I.; Liland, N.S.; Gjesdal, P.; Biancarosa, I.; Menchetti, E.; Li, Y.; Waagbø, R.; Krogdahl, Å.; Lock, E.-J. Black soldier fly larvae meal can replace fish meal in diets of sea-water phase Atlantic salmon (Salmo salar). Aquaculture 2019, 503, 609–619. [Google Scholar] [CrossRef]
  28. Tibbetts, S.M.; Scaife, M.A.; Armenta, R.E. Apparent digestibility of proximate nutrients, energy and fatty acids in nutritionally-balanced diets with partial or complete replacement of dietary fish oil with microbial oil from a novel Schizochytrium sp. (T18) by juvenile Atlantic salmon (Salmo salar L.). Aquaculture 2020, 520, 735003. [Google Scholar]
  29. Santigosa, E.; Olsen, R.E.; Madaro, A.; Trichet, V.V.; Carr, I. Algal oil gives control of long-chain omega-3 levels in full-cycle production of Atlantic salmon, without detriment to zootechnical performance and sensory characteristics. J. World Aquacult. Soc. 2023, 2023, 1–21. [Google Scholar] [CrossRef]
  30. Wei, M.; Parrish, C.C.; Guerra, N.I.; Armenta, R.E.; Colombo, S.M. Extracted microbial oil from a novel Schizochytrium sp. (T18) as a sustainable high DHA source for Atlantic salmon feed: Impacts on growth and tissue lipids. Aquaculture 2021, 534, 736249. [Google Scholar] [CrossRef]
  31. Bolivar, R.B.; Vera Cruz, E.M.; Jimenez, E.B.T.; Sayco, R.M.V.; Argueza, R.L.B.; Ferket, P.R.; Stark, C.R.; Malheiros, R.; Ayoola, A.A.; Johnstone, W.M., III; et al. Feeding Reduction Strategies and Alternative Feeds to Reduce Production Costs of Tilapia Culture; Tech Rep Invest 20007–2009; AquaFish CRSP, Oregon State University: Corvallis, OR, USA, 2010. [Google Scholar]
  32. Skiba, S.; Médale, F.; Kaushik, S.; Lemarié, S.; Gaunand, A. Replacement of Marine Ingredients by Plant Products in Fish Diets; [Technical Report] Inconnu. 2015, p. 25; hal-01901445. Available online: hal.science/hal-01901445/document (accessed on 10 November 2023).
  33. Savonitto, G.; Barkan, R.; Harpaz, S.; Neori, A.; Chernova, H.; Terlizzi, A.; Guttman, L. Fishmeal replacement by periphyton reduces the fish in fish out ratio and alimentation cost in gilthead sea bream Sparus aurata. Sci. Rep. 2021, 11, 20990. [Google Scholar] [CrossRef]
  34. Risius, A.; Janssen, M.; Hamm, U. Consumer preferences for sustainable aquaculture products: Evidence from in-depth interviews, think aloud protocols and choice experiments. Appetite 2017, 113, 246–254. [Google Scholar] [CrossRef]
  35. Zander, K.; Feucht, Y. Consumers’ WTP for sustainable seafood made in Europe. J. Int. Food Agribus. Mark 2018, 30, 251–275. [Google Scholar] [CrossRef]
  36. Hynes, S.; Ravagnan, E.; Gjerstad, B. Do concerns for the environmental credentials of salmon aquaculture translate into WTP a price premium for sustainably farmed fish? A contingent valuation study in Ireland and Norway. Aquacult. Int. 2019, 27, 1709–1723. [Google Scholar] [CrossRef]
  37. Asche, F.; Larsen, T.; Smith, M.; Sogn-Grundvåg, G.; Young, J. Pricing of eco-labels with retailer heterogeneity. Food Policy 2015, 53, 82–93. [Google Scholar] [CrossRef]
  38. Ankamah-Yeboah, I.; Nielsen, M.; Nielsen, R. Price premium of organic salmon in Danish retail sale. Ecol. Econ. 2016, 122, 54–60. [Google Scholar] [CrossRef]
  39. Olesen, I.; Alfnes, F.; Rora, M.B.; Kolstad, K. Eliciting consumers’ WTP for organic and welfare-labelled salmon in a non-hypothetical choice experiment. Livest. Sci. 2010, 127, 218–226. [Google Scholar] [CrossRef]
  40. Ferfolja, M.; Cerjak, M.; Matulić, D.; Tomić Maksan, M. Consumer knowledge and perception about fresh fish from organic farming in Croatia. Cro. J. Fish 2022, 80, 7–16. [Google Scholar] [CrossRef]
  41. Chen, X.; Alfnes, F.; Rickertsen, K. Consumer preferences, ecolabels, and effects of negative environmental information. AgBioForum 2015, 18, 327–336. [Google Scholar]
  42. Hardy, R.W.; Scott, T.M.; Harrell, L.W. Replacement of herring oil with menhaden oil, soybean oil, or tallow in the diets of Atlantic salmon raised in marine net-pens. Aquaculture 1987, 65, 267–277. [Google Scholar] [CrossRef]
  43. Davidson, J.; Kenney, P.B.; Barrows, F.T.; Good, C.; Summerfelt, S.T. Fillet quality and processing attributes of postsmolt Atlantic salmon, Salmo salar, fed a fishmeal-free diet and a fishmeal-based diet in recirculation aquaculture systems. J. World Aquacult. Soc. 2018, 49, 183–196. [Google Scholar] [CrossRef]
  44. Kousoulaki, K.; Østbye, T.K.K.; Krasnov, A.; Torgersen, J.S.; Mørkøre, T.; Sweetman, J. Metabolism, health and fillet nutritional quality in Atlantic salmon (Salmo salar) fed diets containing n-3-rich microalgae. J. Nutr. Sci. 2015, 4, e24. [Google Scholar] [CrossRef]
  45. Kousoulaki, K.; Gerd, M.B.; Mørkøre, T.; Krasnov, A.; Baeverfjord, G.; Ytrestøyl, T.; Carlehög, M.; Sweetman, J.; Ruyter, B. Microalgal Schizochytrium limacinum biomass improves growth and filet quality when used long-term as a replacement for fish oil, in modern salmon diets. Front. Mar. Sci. 2020, 7, 57. [Google Scholar] [CrossRef]
  46. Zatti, K.M.; Ceballos, M.J.; Vega, V.V.; Denstadli, V. Full replacement of fish oil with algae oil in farmed Atlantic salmon (Salmo salar)—Debottlenecking omega 3. Aquaculture 2023, 574, 739653. [Google Scholar] [CrossRef]
  47. Einen, O.; Mørkøre, T.; Rørå, A.M.B.; Thomassen, M.S. Feed ration prior to slaughter—A potential tool for managing product quality of Atlantic salmon (Salmo salar). Aquaculture 1999, 178, 149–169. [Google Scholar] [CrossRef]
  48. Frederick, C.; Brady, D.C.; Bricknell, I. Landing strips: Model development for estimating body surface area of farmed Atlantic salmon (Salmo salar). Aquaculture 2017, 473, 299–302. [Google Scholar] [CrossRef]
  49. MacLean, A. Compensatory Growth, Life-History Decisions and Welfare of Farmed Atlantic Salmon (Salmo salar L.) parr. Ph.D. Thesis, Division of Environmental and Evolutionary Biology, Institute of Biomedical and Life Sciences, University of Glasgow, Glasgow, Scotland, 1999; 165p. [Google Scholar]
  50. Bass, N.; Wall, T. A Standard Procedure for the Field Monitoring of Cataracts in Farmed Atlantic Salmon and Other Species; BIM, Irish Sea Fisheries Board, Dun Laoghaire, Co.: Dublin, Ireland, 2008; p. 3. [Google Scholar]
  51. Kindschi, G.A.; Shaw, H.T.; Bruhn, D.S. Effect of diet on performance, fin quality and dorsal skin lesions in steelhead. J. Appl. Aquacult. 1991, 1, 113–120. [Google Scholar] [CrossRef]
  52. MacLean, A.; Metcalfe, N.B.; Mitchell, D. Alternative competitive strategies in juvenile Atlantic salmon (Salmo salar): Evidence from fin damage. Aquaculture 2000, 184, 291–302. [Google Scholar] [CrossRef]
  53. Browning, H. Improving welfare assessment in aquaculture. Front. Vet Sci Sec. Anim. Behav. Welf. 2023, 10, 1060720. [Google Scholar] [CrossRef] [PubMed]
  54. Savoca, M.S.; Brodie, S.; Welch, H.; Hoover, A.; Benaka, L.R.; Bograd, S.J.; Hazen, E.L. Comprehensive bycatch assessment in US fisheries for prioritizing management. Nat Sust. 2020, 3, 472–480. [Google Scholar] [CrossRef]
  55. Huntington, T. Best Practice Framework for the Management of Aquaculture gear; Global Ghost Gear Initiative—Ocean Conservancy: Washington, DC, USA, 2021; p. 81. [Google Scholar]
  56. HRAT. Does It Do What It Says on the Tin? Fisheries and Aquaculture Certification, Standards and Ratings Ecosystem: An Independent Review; Human Rights at Sea: Havant, UK, 2023; p. 33. [Google Scholar]
  57. US Department of Labor-International Bureau of Labor Affairs. List of Goods Produced by Child Labor or Forced Labor. 2020. Available online: https://www.dol.gov/agencies/ilab/reports/child-labor/list-of-goods (accessed on 10 November 2023).
  58. Nakamura, K.; Ota, Y.; Blaha, F. A practical take on the duty to uphold human rights in seafood workplaces. Mar. Policy 2022, 135, 104844. [Google Scholar] [CrossRef]
  59. Gephart, J.A.; Henriksson, P.J.G.; Parker, R.W.R.; Shepon, A.; Gorospe, K.D.; Bergman, K.; Eshel, G.; Golden, C.D.; Halpern, B.S.; Hornborg, S.; et al. Environmental performance of blue foods. Nature 2021, 507, 360–366. [Google Scholar] [CrossRef]
  60. Ersdal, C.; Midtlyng, P.J.; Jarp, J. An epidemiological study of cataracts in seawater farmed Atlantic salmon Salmo salar. Dis. Aquat. Org. 2001, 45, 229–236. [Google Scholar] [CrossRef]
  61. Bjerkås, E.; Holst, J.C.; Bjerkås, I. Cataract in farmed and wild Atlantic salmon (Salmo salar L.). Anim. Eye Res. 2004, 23, 3–13. [Google Scholar]
  62. Sissener, N.H.; Hamre, K.; Fjelldal, P.G.; Philip, A.J.P.; Espe, M.; Miao, L.; Høglund, E.; Sørensen, C.; Skjærven, K.H.; Holen, E.; et al. Can improved nutrition for Atlantic salmon in freshwater increase fish robustness, survival and growth after seawater transfer? Aquaculture 2021, 542, 736852. [Google Scholar] [CrossRef]
  63. Tröße, C. Mechanisms of Cataract Development in Adult Atlantic Salmon Growers Relative to Dietary Histidine and Plant Feed Ingredients. Ph.D. Thesis, University of Bergen, Bergen, Norway, 2010. [Google Scholar]
  64. Remø, S.C.; Hevroy, E.M.; Olsvik, P.A.; Fontanillas, R.; Breck, O.; Waagbo, R. Dietary histidine requirement to reduce the risk and severity of cataracts is higher than the requirement for growth in Atlantic salmon smolts, independently of the dietary lipid source. Br. J. Nutr. 2014, 111, 1759–1772. [Google Scholar] [CrossRef]
  65. Cañon Jones, H.A.; Noble, C.; Damsgård, B.; Pearce, G.P. Social network analysis of the behavioural interactions that in uence the development of n damage in Atlantic salmon parr (Salmo salar) held at different stocking densities. Appl. Anim. Behv. Sci. 2011, 113, 117–126. [Google Scholar] [CrossRef]
  66. Soderberg, R.W.; Meade, J.W. Effects of rearing density on growth, survival, and fin condition of Atlantic salmon. Prog. FishCult. 1987, 49, 280–283. [Google Scholar] [CrossRef]
  67. Ellis, T.; Oidtmann, B.; St-Hilaire, S.; Turnbull, J.F.; North, B.P.; MacIntyre, C.M.; Nikolaidis, J.; Hoyle, I.; Kestin, S.C.; Knowles, T.G. Fin erosion in farmed fish. In Fish Welfare; Branson, E.J., Ed.; Blackwell Publishing Ltd.: Oxford, UK, 2008; pp. 121–149, 300. [Google Scholar]
  68. Larsen, M.H.; Nemitz, A.; Steinheuer, M.; Lysdale, J.; Thomassen, S.T.; Holdensgaard, G. Effects of Hatchery Feeding Practices on Fin and Operculum Condition of Juvenile Atlantic Salmon Salmo salar. 2018, p. 22. Available online: https://danmarksvildlaks.dk/wp-content/uploads/2018/04/Technical-report_feeding_opercula.pdf (accessed on 3 November 2023).
  69. Ellis, M.A. Fin Damage in Juvenile Atlantic Salmon: Farm and Experimental, Causes and Consequences. Ph.D. Thesis, University of Stirling, Institute of Aquaculture, Stirling, Scotland, 2019; p. 265. [Google Scholar]
  70. Timmerhaus, G.; Lazado, C.C.; Cabillon, N.A.R.; Reiten, B.K.M.; Johansen, L.-H. The optimum velocity for Atlantic salmon post-smolts in RAS is a compromise between muscle growth and fish welfare. Aquaculture 2021, 532, 7360765. [Google Scholar] [CrossRef]
  71. Lemm, C.A.; Rottiers, D.S.; Dropkin, D.S.; Dennison, B.A. Growth, composition, and fin quality of Atlantic Salmon fed different diets at seasonal temperatures in a laboratory and hatchery. US Fish Wildl. Serv. Biol. Rep. 1988, 88, 1–12. [Google Scholar]
  72. Bourne, M. Texture profile analysis. Food Technol. 1978, 32, 62–66. [Google Scholar]
  73. Latremouille, D.N. Fin erosion in aquaculture and natural environments. Rev. Fish Sci. 2003, 11, 315–335. [Google Scholar] [CrossRef]
  74. Cañon Jones, H.A.; Noble, C.; Damsgård, B.; Pearce, G.P. Evaluating the effects of a short-term feed restriction period on the behaviour and welfare of Atlantic salmon (Salmo salar) parr using social network analysis and fin damage. J. World Aquacult. Soc. 2017, 48, 35–45. [Google Scholar] [CrossRef]
  75. Hoyle, I.; Oidtmann, B.; Ellis, T.; Turnbull, J.; North, B.; Nikolaidis, J.; Knowles, T.G. A validated macroscopic key to assess fin damage in farmed rainbow trout (Onchorynchus mykiss). Aquaculture 2007, 270, 142–148. [Google Scholar] [CrossRef]
  76. Noble, C.; Kadri, S.; Mitchell, D.F.; Huntingford, F.A. The effect of feed regime on the growth and behaviour of 1+ Atlantic salmon post-smolts (Salmo salar L.) in semi-commercial sea cages. Aquacul. Res. 2007, 38, 1686–1691. [Google Scholar] [CrossRef]
  77. Noble, C.; Kadri, S.; Mitchell, D.F.; Huntingford, F.A. Growth, production and fin damage in cage-held 0+ Atlantic salmon pre-smolts (Salmo salar L.) fed either (a) on-demand, or (b) to a fixed satiation–restriction regime: Data from a commercial farm. Aquaculture 2008, 275, 163–168. [Google Scholar] [CrossRef]
  78. Amoroso, G.; Nguyen, C.D.H.; Vo, T.T.M.; Ventura, T.; Elizur, A. Understanding Flesh Colour Variation in Atlantic Salmon: Molecular Mechanisms and Genetic Effect. 2020, p. 201. Available online: https://www.frdc.com.au/project/2014-248 (accessed on 2 November 2023).
  79. Sylvia, G.; Morrisey, M.T.; Graham, T.; Garcia, S. Organoleptic qualities of farmed and wild salmon. J. Aquat. Food Prod. Technol. 1995, 4, 51–64. [Google Scholar] [CrossRef]
  80. Storebakken, T.; Foss, P.; Schiedt, K.; Austreng, E.; Liaaen-Jensen, S.; Mans, U. Carotenoids in diets for salmonids. IV. Pigmentation of Atlantic salmon with astaxanthin, astaxanthin dipalmitate and canthaxanthin. Aquaculture 1987, 65, 279–292. [Google Scholar] [CrossRef]
  81. Bjerkeng, B.; Refstie, S.; Fjalestad, K.T.; Storebakken, T.; Rodbotten, M.; Roem, A.J. Quality parameters of the flesh of Atlantic salmon (Salmo salar) as affected by dietary fat content and full-fat soybean meal as a partial substitute for fish meal in the diet. Aquaculture 1997, 157, 297–309. [Google Scholar] [CrossRef]
  82. Buttle, L.G.; Crampton, V.O.; Williams, P.D. The effect of feed pigment type on flesh pigment deposition and colour in farmed Atlantic salmon, Salmo salar L. Aquacult. Res. 2001, 32, 103–111. [Google Scholar] [CrossRef]
  83. Young, A.; Morris, P.C.; Huntingford, F.A.; Sinnott, R. The effects of diet, feeding regime and catch-up growth on fl esh quality attributes of large (1 + sea winter) Atlantic salmon, Salmo salar. Aquaculture 2005, 248, 59–73. [Google Scholar] [CrossRef]
  84. Sinnott, R. Carcass quality monitoring at the farm and factory. In Farmed Fish Quality; Kestin, S.C., Warrriss, P.D., Eds.; Blackwell Science: Osney Mead, UK, 2001; pp. 318–334, 430. [Google Scholar]
  85. de Francesco, M.; Parisi, G.; Medale, F.; Lupi, P.; Kaushik, S.J.; Poli, B.M. Effect of long-term feeding with a plant protein mixture based diet on growth and body/fillet quality traits of large rainbow trout Oncorhynchus mykiss. Aquaculture 2004, 236, 413–429. [Google Scholar] [CrossRef]
  86. D’Souza, N.; Skonberg, D.I.; Stone, D.A.J.; Brown, P.B. Effect of soybean meal-based diets on the product quality of rainbow trout fillets. J. Food Sci. 2006, 71, S337–S342. [Google Scholar] [CrossRef]
  87. Johnsen, C.A.; Hagen, Ø.; Bendiksen, E.Å. Long-term effects of high-energy, low-fishmeal feeds on growth and flesh characteristics of Atlantic salmon (Salmo salar L.). Aquaculture 2011, 312, 109–116. [Google Scholar] [CrossRef]
  88. Liu, K.K.M.; Barrows, F.T.; Hardy, R.W.; Dong, F.M. Body composition, growth performance, and product quality of rainbow trout (Oncorhynchus mykiss) fed diets containing poultry fat, soybean/corn lecithin, or menhaden oil. Aquaculture 2004, 238, 309–328. [Google Scholar] [CrossRef]
  89. Kwan, D.; Dai, L.; Liu, D.; Liu, H.; Du, W. Efficient biodiesel conversion from microalgae oil of Schizochytrium sp. Catalysts 2019, 9, 341. [Google Scholar] [CrossRef]
  90. Casas, C.; Martinez, O.; Guillen, M.D.; Pin, C.; Salmeron, J. Textural properties of raw Atlantic salmon (Salmo salar) at three points along the fillet, determined by different methods. Food Control 2006, 17, 511–515. [Google Scholar] [CrossRef]
  91. Sigurgisladottir, S.; Hafsteinsson, H.; Jonsson, A.; Lie, Ø.; Nortvedt, R.; Thomassen, M.S.; Torrissen, O. Textural properties of raw salmon fillets as related to sampling method. J. Food Sci. 1999, 64, 99–104. [Google Scholar] [CrossRef]
  92. Jonsson, A.; Sigurgisladottir, S.; Hafsteinson, H.; Kristbergsson, K. Textural properties of raw Atlantic salmon (Salmo salar) fillets measured by different methods in comparison to expressible moisture. Aquacult. Nutr. 2001, 7, 81–89. [Google Scholar] [CrossRef]
  93. Merkin, G.V.; Stein, L.H.; Pittman, K.; Nortvedt, R. The effect of stunning methods and season on muscle texture hardness in Atlantic salmon (Salmo salar L.). J. Food Sci. 2014, 79, E1137–E1141. [Google Scholar] [CrossRef]
  94. Larsson, T.; Koppang, E.O.; Espe, M.; Terjesen, B.F.; Krasnov, A.; Moreno, H.M.; Rørvik, K.-A.; Thomassen, M.; Mørkøre, T. Fillet quality and health of Atlantic salmon (Salmo salar L.) fed a diet supplemented with glutamate. Aquaculture 2014, 426, 288–295. [Google Scholar] [CrossRef]
  95. Ostbye, T.K.K.; Ruyter, B.; Standal, I.B.; Stien, L.H. Functional amino acids stimulate muscle development and improve fillet texture of Atlantic salmon. Aquacult. Nutr. 2018, 24, 14–26. [Google Scholar] [CrossRef]
  96. Azm, F.R.A.; Kong, F.; Wang, X.; Zhu, W.; Yu, H.; Long, X.; Tan, Q. The interaction of dried distillers grains with solubles (DDGS) type and level on growth performance, health, texture, and muscle-related gene expression in grass carp (Ctenopharyngodon idellus). Front. Nutr. Sec. Nutr. Sustain. Diets 2022, 28, 832651. [Google Scholar] [CrossRef]
  97. Hu, Y.; Hu, Y.; Wu, T.; Chu, W. Effects of high dietary levels of cottonseed meal and rapeseed meal on growth performance, muscle texture, and expression of muscle-related genes in grass carp. N. Am. J. Aquacult. 2019, 81, 235–241. [Google Scholar] [CrossRef]
  98. Kong, F.; Azm, F.R.A.; Wang, X.; Zhu, Y.; Yu, H.; Yao, J.; Luo, Z.; Tan, Q. Effects of replacement of dietary cottonseed meal by distiller’s dried grains with solubles on growth performance, muscle texture, health and expression of muscle-related genes in grass carp (Ctenopharyngodon idellus). Aquacult Nutr. 2021, 27, 13266. [Google Scholar] [CrossRef]
  99. Wu, F.; Tian, J.; Yu, L.; Wen, H.; Jiang, M.; Lu, X. Effects of dietary rapeseed meal levels on growth performance, biochemical indices and flesh quality of juvenile genetically improved farmed tilapia. Aquacult. Rep. 2021, 20, 100679. [Google Scholar] [CrossRef]
  100. Mørkøre, T.; Moreno, H.M.; Borderías, J.; Larsson, T.; Hellberg, H.; Hatlen, B.; Romarheim, O.H.; Ruyter, B.; Lazado, C.C.; Jiménez-Guerrero, R.; et al. Dietary inclusion of Antarctic krill meal during the finishing feed period improves health and fillet quality of Atlantic salmon (Salmo salar L.). Br. J. Nutr. 2020, 124, 418–431. [Google Scholar] [CrossRef] [PubMed]
  101. Sigurgisladottir, S.; Torrissen, O.; Lie, Ø.; Thomassen, M.; Hafsteinsson, H. Salmon quality: Methods to determine the quality parameters. Rev. Fish Sci. 1997, 5, 223–252. [Google Scholar] [CrossRef]
  102. Zhu, F.; Peng, J.; Gao, J.; Zhao, Y.; Yu, K.; He, Y. Determination and visualization of fat contents in salmon fillets based on visible and near-infrared hyperspectral imagery. Trans. Chin. Soc. Ag. Eng. 2014, 30, 314–323. [Google Scholar]
  103. Einen, O.; Waagan, B.; Thomassen, M.S. Starvation prior to slaughter in Atlantic salmon (Salmo salar) I. Effects on weight loss, body shape, slaughter- and fillet-yield, proximate and fatty acid composition. Aquaculture 1998, 166, 85–104. [Google Scholar] [CrossRef]
  104. Nøstbakken, O.J.; Reksten, A.M.; Hannisdal, R.; Dahl, L.; Duinker, A. Sampling of Atlantic salmon using the Norwegian Quality cut (NQC) vs. whole fillet; differences in contaminant and nutrient contents. Food Chem. 2023, 418, 136056. [Google Scholar] [CrossRef]
  105. Ares, G.; Varela, P. Trained vs. consumer panels for analytical testing: Fueling a long lasting debate in the field. Food Qual. Prefer 2017, 61, 79–86. [Google Scholar] [CrossRef]
  106. Calanche, J.B.; Beltrán, J.B.; Arias, A.J.H. Aquaculture and sensometrics: The need to evaluate sensory attributes and the consumers’ preferences. Rev. Aquacult. 2020, 12, 805–821. [Google Scholar] [CrossRef]
  107. Chambers, E.I.V.; Smith, E.A. Effects of testing experience on performance of trained sensory panelists. J. Sens. Stud. 1993, 8, 155–166. [Google Scholar]
  108. Elgaard, L.; Jensen, S.; Mielby, L.A.; Byrne, D.V. Performance of beer sensory panels: A comparison of experience level, product knowledge, and responsiveness to feedback calibration. J. Sens. Stud. 2019, 34, e12540. [Google Scholar] [CrossRef]
  109. Roberts, A.K.; Vickers, Z.M. A comparison of trained and untrained judges, evaluation of sensory attribute intensities and liking of Cheddar cheeses. J. Sens. Stud. 1994, 9, 1–20. [Google Scholar] [CrossRef]
  110. Carlucci, D.; Nocella, G.; De Devitiis, B.; Viscecchia, R.; Bimbo, F.; Nardone, G. Consumer purchasing behaviour towards fish and seafood products. Patterns and insights from a sample of international studies. Appetite 2015, 84, 212–227. [Google Scholar] [CrossRef] [PubMed]
  111. Altintzoglou, T.; Cordeiro, C.M.; Honkanen, P.; Onozaka, Y. “It gives me peace of mind”. A new perspective on the identification of quality cues on salmon fillet products in Japan and the USA. Aquaculture 2022, 554, 728112. [Google Scholar] [CrossRef]
  112. Tomić, M.; Kovačićek, T.; Matulić, D. Attitudes as basis for segmenting Croatian fresh fish consumers. New Medit. 2016, 4, 63–71. [Google Scholar]
  113. Verbeke, W.; Vackier, I. Individual determinants of fish consumption: Application of the theory of planned behaviour. Appetite 2005, 44, 67–82. [Google Scholar] [CrossRef]
  114. Al-Saghir, S.; Thurner, K.; Wagner, K.-H.; Frisch, G.; Luf, W.; Razzazi-Fazell, E.; Elmadfa, I. Effects of different cooking procedures on lipid quality and cholesterol oxidation of farmed salmon fish (Salmo salar). J. Agric. Food Chem. 2004, 52, 5290–5296. [Google Scholar] [CrossRef]
  115. Gladyshev, M.I.; Sushchik, N.N.; Gubanenko, G.A.; Demirchieva, S.M.; Kalachova, G.S. Effect of way of cooking on content of essential polyunsaturated fatty acids in muscle tissue of humpback salmon (Oncorhynchus gorbuscha). Food Chem. 2006, 96, 446–451. [Google Scholar] [CrossRef]
  116. Larsen, D.; Quek, S.Y.; Eyres, L. Effect of cooking method on the fatty acid profile of New Zealand King Salmon (Oncorhynchus tshawytscha). Food Chem. 2010, 119, 785–790. [Google Scholar] [CrossRef]
  117. Shearer, K.D. Factors affecting the proximate composition of cultured fishes with emphasis on salmonids. Aquaculture 1994, 119, 63–88. [Google Scholar] [CrossRef]
  118. Einen, O.; Skrede, G. Quality characteristics in raw and smoked fillets of Atlantic salmon, Salmo salar, fed high-energy diets. Aquacult. Nutr. 1998, 4, 99–108. [Google Scholar] [CrossRef]
  119. Turchini, G.M.; Francis, D.S.; Du, Z.-Y.; Olsen, R.E.; Ringø, E.; Tocher, D.R. The lipids. In Fish Nutrition; Hardy, R.W., Kaushik, S., Eds.; Academic Press: San Diego, CA, USA, 2022; pp. 303–467. [Google Scholar]
  120. Wang, Z.; Qiao, F.; Zhang, W.-B.; Parisi, G.; Du, Z.-Y.; Zhang, M.-L. The flesh texture of teleost fish: Characteristics and interventional strategies. Rev. Aquac. 2023, 16, 12849. [Google Scholar] [CrossRef]
  121. Drewnowski, A. Taste preferences and food intake. Annu. Rev. Nutr. 1997, 17, 237–253. [Google Scholar] [CrossRef] [PubMed]
  122. Methven, L.; Allen, V.J.; Withers, C.A.; Gosney, M.A. Ageing and taste. Proc. Nutr. Soc. 2012, 71, 556–565. [Google Scholar] [CrossRef] [PubMed]
  123. Ogawa, T.; Annear, M.J.; Ikebe, K.; Maeda, Y. Taste-related sensations in old age. J. Oral Rehabil. 2017, 44, 626–635. [Google Scholar] [CrossRef] [PubMed]
  124. Wang, J.-J.; Liang, K.-L.; Lin, W.-J.; Chen, C.-Y.; Jiang, R.S. Influence of age and sex on taste function of healthy subjects. PLoS ONE 2020, 15, e0227014. [Google Scholar] [CrossRef] [PubMed]
  125. Gidhini, S.; Varrà, M.O.; Zanardi, E. Approaching authenticity issues in fish and seafood products by qualitative spectroscopy and chemometrics. Molecules 2019, 24, 1812. [Google Scholar] [CrossRef]
  126. Hikima, J.I.; Ando, M.; Hamaguchi, H.O.; Sakai, M.; Maita, M.; Yazawa, K.; Takeyama, H.; Aoki, T. On-site direct detection of astaxanthin from salmon fillet using Raman spectroscopy. Mar. Biotech. 2017, 19, 157–163. [Google Scholar] [CrossRef]
  127. Fiorino, G.M.; Losito, I.; De Angelis, E.; Arlorio, M.; Logrieco, A.F.; Monaci, L. Assessing fish authenticity by direct analysis in real time-high resolution mass spectrometry and multivariate analysis: Discrimination between wild-type and farmed salmon. Food Res. Int. 2019, 116, 1258–1265. [Google Scholar] [CrossRef]
  128. Chen, Z.; Wu, T.; Xiang, C.; Xu, X.; Tian, X. Rapid identification of rainbow trout adulteration in Atlantic salmon by Raman spectroscopy combined with machine learning. Molecules 2019, 24, 2851. [Google Scholar] [CrossRef]
  129. Han, C.; Dong, S.L.; Li, L.; Gao, Q. Efficacy of using stable isotopescoupled with chemometrics to differentiate the production method and geographical origin of farmed salmonids. Food Chem. 2021, 364, 130364. [Google Scholar] [CrossRef] [PubMed]
  130. Han, C.; Li, L.; Dong, X.; Gao, Q.; Dong, S. Current progress in the authentication of fishery and aquatic products using multi-element and stable isotope analyses combined with chemometrics. Rev. Aquacult. 2022, 14, 2023–2037. [Google Scholar] [CrossRef]
  131. Wang, Y.V.; Wan, A.H.L.; Lock, E.-J.; Andersen, N.; Winter-Schuh, C.; Larsen, T. Know your fish: A novel compound-specific isotope approach for tracing wild and farmed salmon. Food Chem. 2018, 256, 380–389. [Google Scholar] [CrossRef] [PubMed]
  132. Wang, C.; Bi, H. Super-fast seafood authenticity analysis by One-step pretreatment and comparison of mass spectral patterns. Food Control 2021, 123, 107751. [Google Scholar] [CrossRef]
  133. McLean, E.; Fredriksen, L.; Alfrey, K.; Tlusty, M.F.; Barrows, F.T. Growth, integrity, and consumer acceptance of largemouth bass, Micropterus salmoides (Lacépède, 1802), fed marine resource-free diets. Int. J. Fish. Aquat. Stud. 2020, 8, 365–369. [Google Scholar] [CrossRef]
Figure 1. The effect of experimental diets on fin erosion was assessed using a categorical method based on an ordinal scale of 0–4 as suggested by Person Le-Ruyet et al. [52]. Arrows indicate positions of posterior-most intact rays.
Figure 1. The effect of experimental diets on fin erosion was assessed using a categorical method based on an ordinal scale of 0–4 as suggested by Person Le-Ruyet et al. [52]. Arrows indicate positions of posterior-most intact rays.
Fishes 09 00037 g001
Figure 2. Isotope values for δ15N and δ13C, for Atlantic salmon post-smolts fed one of seven diets. Values are means + 95% confidence intervals. For A, P, and C diet formulations see [6].
Figure 2. Isotope values for δ15N and δ13C, for Atlantic salmon post-smolts fed one of seven diets. Values are means + 95% confidence intervals. For A, P, and C diet formulations see [6].
Fishes 09 00037 g002
Figure 3. Differences in fillet preference, by gender. Fish fed the P3 diet (for formulations see [6]) were favored by both sexes. NP = no preference.
Figure 3. Differences in fillet preference, by gender. Fish fed the P3 diet (for formulations see [6]) were favored by both sexes. NP = no preference.
Fishes 09 00037 g003
Table 1. Ethnicity, gender, and age-group breakdown of thirty-four untrained taste testers employed during the organoleptic evaluation of the various salmon fillets.
Table 1. Ethnicity, gender, and age-group breakdown of thirty-four untrained taste testers employed during the organoleptic evaluation of the various salmon fillets.
FemaleMale
EthnicityCaucasian415
African/Afro-American22
(Eur)Asian71
Latino/Hispanic 3
Age group18–2421
25–3426
35–4436
45–5422
55–6424
65+22
Table 2. The impact of dietary treatments (±SD) on morphometric and fillet characteristics of post-smolt Atlantic salmon. Data in a row displaying different superscripts were significantly different (p < 0.05). K = condition factor; HG wt = headed and gutted weight. For comprehensive diet formulations see [6].
Table 2. The impact of dietary treatments (±SD) on morphometric and fillet characteristics of post-smolt Atlantic salmon. Data in a row displaying different superscripts were significantly different (p < 0.05). K = condition factor; HG wt = headed and gutted weight. For comprehensive diet formulations see [6].
DietC1P1P2P3A1A2A3
Weight (g)603.13 ± 76.95568.75 ± 47.49610.63 ± 58.76606.88 ± 67.03613.75 ± 36.52626.88 ± 61.76605.63 ± 57.54
Length (cm)36.81 ± 1.9335.63 ± 0.7936.81 ± 1.3136.19 ± 1.1036.88 ± 0.6436.69 ± 1.2536.56 ± 1.05
K1.21 ± 0.051.26 ± 0.091.22 ± 0.081.28 ± 0.101.22 ± 0.031.27 ± 0.061.24 ± 0.04
Surface area (cm2)689.16 ± 53.90665.57 ± 34.21694.88 ± 41.16692.08 ± 46.55697.48 ± 25.12706.08 ± 42.67691.45 ± 39.78
Gutted wt550.00 ± 73.29503.13 ± 42.25547.50 ± 57.63553.75 ± 60.58552.50 ± 37.51564.38 ± 56.28545.63 ± 51.30
HG wt (g)501.88 ± 66.44455.50 ± 40.44487.50 ± 54.31500.00 ± 55.16496.88 ± 33.48509.38 ± 50.25493.13 ± 48.10
HG Yield (%)83.00 ± 1.51 a81.13 ± 1.13 b79.88 ± 1.64 b82.50 ± 0.76 a80.88 ± 0.84 b81.25 ± 1.28 a81.38 ± 0.74 a
Fillet wt (g)302.50 ± 43.01273.75 ± 27.22293.75 ± 42.74311.25 ± 46.73305 ± 40.00316.25 ± 39.62303.75 ± 36.23
Fillet yield (%)50.19 ± 4.1348.19 ± 3.5248.02 ± 4.3051.26 ± 4.9649.58 ± 4.5350.42 ± 3.3950.08 ± 2.22
Color back20.88 ± 1.13 a23.88 ± 0.84 b22.75 ± 1.17 a,b23.00 ± 1.07 b22.38 ± 1.19 a,b22.63 ± 1.41 a,b23.00 ± 1.77 b
Color belly20.38 ± 0.74 a22.88 ± 0.84 b21.75 ± 1.17 a,b22.00 ± 1.07 a,b21.38 ± 1.19 a,b21.63 ± 1.41 a,b22.00 ± 1.51 a,b
Color NQC20.88 ± 1.13 a23.88 ± 0.84 b22.63 ± 1.19 a,b23.00 ± 1.07 b22.38 ± 1.19 a,b22.50 ± 1.51 a,b23.00 ± 1.77 b
Table 3. The impact of dietary treatments (±SD) on standard length and dorsal fin characteristics of post-smolt Atlantic salmon. SL = standard length; RFW = relative fin width; RFH = relative fin height; RFI = relative fin index; FW = fray width; #F = number of frays. For comprehensive diet formulations see [6]. Data in a row displaying different superscripts were significantly different (p < 0.05).
Table 3. The impact of dietary treatments (±SD) on standard length and dorsal fin characteristics of post-smolt Atlantic salmon. SL = standard length; RFW = relative fin width; RFH = relative fin height; RFI = relative fin index; FW = fray width; #F = number of frays. For comprehensive diet formulations see [6]. Data in a row displaying different superscripts were significantly different (p < 0.05).
DietC1P1P2P3A1A2A3
SL33.57 ± 17.9 a31.18 ± 10.0 b31.46 ± 11.7 a,b32.09 ± 12.6 a,b33.08 ± 11.3 a,b31.78 ± 17.0 a,b31.46 ± 11.73 b
RFW45.18 ± 3.4942.44 ± 2.8342.75 ± 1.6743.69 ± 3.7445.69 ± 3.1443.69 ± 3.7042.44 ± 2.47
RFH33.88 ± 2.1229.81 ± 3.7730.81 ± 1.8330.94 ± 4.0133.63 ± 3.1430.56 ± 4.2530.63 ± 3.71
RFI13.48 ± 1.0813.60 ± 0.6813.59 ± 0.5013.64 ± 1.3513.80 ± 0.6313.73 ± 0.4913.40 ± 0.71
FW3.50 ± 2.691.63 ± 2.152.00 ± 1.691.81 ± 2.070.75 ± 1.492.81 ± 4.002.31 ± 2.74
#F2.75 ± 2.250.88 ± 0.992.00 ± 2.391.00 ± 1.691.25 ± 3.152.00 ± 2.561.00 ± 1.31
Table 4. The impact of various dietary treatments on mean (±SD) stable isotope concentrations of δ13C and δ15N and δ13C: δ13N ratios in fillets of post-smolt Atlantic salmon. For comprehensive diet formulations see [6]. Data in a row displaying different superscripts were significantly different (p < 0.05).
Table 4. The impact of various dietary treatments on mean (±SD) stable isotope concentrations of δ13C and δ15N and δ13C: δ13N ratios in fillets of post-smolt Atlantic salmon. For comprehensive diet formulations see [6]. Data in a row displaying different superscripts were significantly different (p < 0.05).
DietC1P1P2P3A1A2A3
δ13C−19.3 ± 0.3 a−20.0 ± 0.2 b−20.6 ± 0.4 b−21.1 ± 0.4 c−20.6 ± 0.3 b−20.9 ± 0.4 c−20.9 ± 0.3 c
δ15N10.8 ± 0.4 a6.7 ± 0.2 b6.4 ± 0.3 b6.2 ± 0.3 b6.2 ± 0.1 b6.3 ± 0.2 b6.6 ± 0.2 b
δ13C: δ15N−1.8 ± 0.1 a−3.0 ± 0.1 b−3.2 ± 0.2 b−3.4 ± 0.2 b−3.3 ± 0.1 b−3.3 ± 0.1 b−3.2 ± 0.1 b
Table 5. Mean (±SE) measurements for various texture variables taken from the anterior section of fillets of post-smolt Atlantic salmon fed on different diets over a 90-day period. For comprehensive diet formulations see [6].
Table 5. Mean (±SE) measurements for various texture variables taken from the anterior section of fillets of post-smolt Atlantic salmon fed on different diets over a 90-day period. For comprehensive diet formulations see [6].
DietHardnessCohesivenessSpringinessResilience
C1638.0 ± 34.640.9 ± 1.499.9 ± 0.113.7 ± 0.7
P1610.5 ± 41.637.2 ± 1.299.9 ± 0.011.5 ± 0.5
P2608.5 ± 40.441.1 ± 1.5100.2 ± 0.313.4 ± 1.3
P3536.0 ± 25.138.9 ± 1.5100.0 ± 0.012.2 ± 0.8
A1633.4 ± 17.238.9 ± 0.8100.6 ± 0.514.4 ± 1.3
A2552.8 ± 45.439.7 ± 1.8100.1 ± 0.213.3 ± 0.8
A3537.8 ± 45.439.2 ± 1.4101.6 ± 1.316.1 ± 2.7
Table 6. Mean (±SE) measurements for various texture variables taken from the posterior section of fillets of post-smolt Atlantic salmon fed on different diets over a 90-day period. For comprehensive diet formulations see [6]. Data in a row displaying different superscripts were significantly different (p < 0.05).
Table 6. Mean (±SE) measurements for various texture variables taken from the posterior section of fillets of post-smolt Atlantic salmon fed on different diets over a 90-day period. For comprehensive diet formulations see [6]. Data in a row displaying different superscripts were significantly different (p < 0.05).
DietHardnessCohesivenessSpringinessResilience
C1764.3 ± 133.538.3 ± 1.2100.2 ± 0.3 b13.3 ± 1.0 a,b
P1691.5 ± 62.835.6 ± 1.699.8 ± 0.0 b10.9 ± 0.5 b
P2681.5 ± 63.638.3 ± 1.599.9 ± 0.0 b12.8 ± 0.9 a,b
P3619.8 ± 73.936.2 ± 1.299.9 ± 0.0 b11.9 ± 0.7 b
A1711.7 ± 41.136.4 ± 1.2102.4 ± 1.0 a17.8 ± 2.6 a
A2729.1 ± 63.237.0 ± 1.499.9 ± 0.0 b12.3 ± 0.6 b
A3659.3 ± 38.536.1 ± 0.999.0 ± 0.0 b11.7 ± 0.6 b
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

McLean, E.; Campbell, K.B.; Kuhn, D.D.; Tlusty, M.F.; Barrows, F.T. The Impact of Marine Resource-Free Diets on Quality Attributes of Atlantic Salmon. Fishes 2024, 9, 37. https://doi.org/10.3390/fishes9010037

AMA Style

McLean E, Campbell KB, Kuhn DD, Tlusty MF, Barrows FT. The Impact of Marine Resource-Free Diets on Quality Attributes of Atlantic Salmon. Fishes. 2024; 9(1):37. https://doi.org/10.3390/fishes9010037

Chicago/Turabian Style

McLean, Ewen, Kelly B. Campbell, David D. Kuhn, Michael F. Tlusty, and Frederick T. Barrows. 2024. "The Impact of Marine Resource-Free Diets on Quality Attributes of Atlantic Salmon" Fishes 9, no. 1: 37. https://doi.org/10.3390/fishes9010037

Article Metrics

Back to TopTop