Astaxanthin deposition in the flesh of Atlantic Salmon, Salmo salar L., in relation to dietary astaxanthin concentration and feeding period

Atlantic salmon, Salmo salar L., were fed nine experimental diets containing from 0 to 200 mg astaxanthin per kg^?1 for six time periods, ranging from 3 to 21 months, in sea cages at Matre Aquaculture Research Station, Matredal, Norway. The sampled fish had an initial mean weight of 115 g and reached a weight of 3.2 kg at the termination of the experiment. Every third month, 10 fish from each dose and time group were sampled and the astaxanthin concentration in the flesh determined. The amount of astaxanthin in the flesh ranged from 0.7 to 8.9 mg kg^?1 at the termination of the experiment. This paper discusses deposition of astaxanthin in the flesh of Atlantic salmon in relation to dietary carotenoid levels in the 0–200 mg kg^?1 range and feeding times of 3–21 months. Under the conditions of this experiment, no significant effect on astaxanthin deposition rate could be achieved by increasing the astaxanthin level above 60 mg kg dry feed^?1. Atlantic salmon should be fed astaxanthin-supplemented diets during the whole seawater stage in order to obtain maximal astaxanthin level in the flesh.     

Atlantic salmon (Salmo salar) postsmolts adapt lipid digestion according to elevated dietary wax esters from Calanus finmarchicus

Wax esters (WE) in copepods constitute huge natural marine lipid resources, which can contribute as future lipid source in formulated diets in aquaculture, and thereby reduce the pressure on use of marine resources at higher trophic levels. The present study was undertaken to investigate factors affecting WE digestibility, including production of bile and lipases in Atlantic salmon fed diets containing high proportions of oil derived from copepods. Individually tagged postsmolt Atlantic salmon (initial weight 250 g) were distributed into three dietary groups in triplicate tanks and fed either a fish oil supplemented diet or diets where 50% or 100% of the fish oil was replaced with oil extracted from Calanus finmarchicus . WE accounted for 30.7% or 47.7% of the lipids in these latter diets, respectively. Over the 100 day feeding period, the salmon fed the fish oil diet displayed a significantly higher specific growth rate (SGR; 0.74) than fish fed the 100% Calanus oil diet (SGR; 0.67). The apparent digestibility coefficient of total lipid and total fatty acids was significantly higher in salmon fed the fish oil and the mixed diet compared to fish fed the pure Calanus oil diet. However, the fish appeared to enhance the lipid digestive capacity by increasing bile volume and the lipolytic activity. It is concluded that the digestion of WE in Atlantic salmon is poorer than for triacylglycerols. However, the digestive capacity is increased by elevating the bile content and lipase activity. At very high levels however, WE of lipid between 37.5% and 47.7%, are there no more compensation and WE utilisation decreases.     

The effect of feed pigment type on flesh pigment deposition and colour in farmed Atlantic salmon, Salmo salar L.

The characteristic pink colour of salmonid flesh is a result of deposition of naturally occurring carotenoid pigments. Achieving successful pigmentation in farmed salmonids is a vital aspect of fish farming and commercial feed production. Currently commercial diets for farmed salmonids contain either or both of the synthetic pigments commercially available, astaxanthin and canthaxanthin. Atlantic salmon, Salmo salar L. ( = 220 g initial weight) were given feeds where the pigment source was astaxanthin only, canthaxanthin only or a astaxanthin/canthaxanthin mix. The rearing environment was 12 × 3 m tanks supplied with sea water at the EWOS research farm Lønningdal, near Bergen, Norway. As the proportion of dietary canthaxanthin increased, flesh pigment levels also showed an increase; the pigment content in the muscle of canthaxanthin‐only fed fish was 0.4 mg kg^?1 (or 14%) higher than that of the astaxanthin‐only fed fish, with the mixed pigment fed fish being intermediate between the two extremes. Results of cross‐section assessment for Minolta colorimeter redness (a*) values and Roche Salmofan^TM scores also showed an increase in colour with increasing proportions of canthaxanthin in the feed. The data reported clearly indicates that S. salar ( = 810 g final weight) of this size deposit canthaxanthin more efficiently than they do astaxanthin. These results contrast with those obtained by other authors with rainbow trout, Oncorynchus mykiss (Walbaum), and imply that the absorption or utilization of the pigments differs between species.     

Digestibility of Calanus finmarchicus wax esters in Atlantic salmon (Salmo salar) freshwater presmolts and seawater postsmolts maintained at constant water temperature

Calanoid copepods are a rich source of marine lipid for potential use in aquafeeds. Copepod oil is primarily composed of wax esters (WE) and there are concerns over the efficiency of wax ester, versus triacylglycerol (TAG), digestion and utilization in fish. As smoltification represents a period of major physiological adaptation, the present study examined the digestibility of a high WE diet ( Calanus oil; 48% WE, 26% TAG), compared with a TAG diet (fish oil; 58% TAG), in Atlantic salmon freshwater presmolts and seawater postsmolts, of similar age (9 months) and weight (112 g and 141 g initial, respectively), over a 98-day period at constant temperature. Fish grew significantly better, and possessed lower feed conversion ratios (FCR), in seawater than freshwater. However, total lipid apparent digestibility coefficient (ADC) values were significantly lower in seawater fish, as were total fasted bile volumes. Dietary Calanus oil also had a significant effect, reducing growth and lipid ADC values in both freshwater and seawater groups. Postsmolts fed dietary Calanus oil had the poorest lipid ADC values and analysis of faecal lipid class composition revealed that 33% of the remaining lipid was WE and 32% fatty alcohols. Dietary prevalent 22:1n-11 and 20:1n-9 fatty alcohols were particularly poorly utilized. A decrease in primary bile acid, taurocholate, concentration was observed in the bile of dietary Calanus oil groups which could be related to the lower cholesterol content of the diet. The dietary WE : TAG ratio is discussed in relation to life stage and biliary intestinal adaptation to the seawater environment postsmoltification.     

Modeling optimal dietary pigmentation strategies in farmed Atlantic salmon: Application of mixed-integer non-linear mathematical programming techniques

The most important visual quality characteristic of Atlantic salmon is the red/pink flesh color. The primary source of this coloration in salmon is caused by deposition of relatively large amounts of pigments, such as astaxanthin, obtained from their diet. Astaxanthin is expensive, and in commercial farming practice, dietary color pigments comprises about 15-20% of the total feed cost. One important operational process in commercial fish farms is therefore to minimize pigment costs. Based on recent models on the effects of dietary pigment concentration and fish size on visual color perception of Atlantic salmon, this study has built a mathematical programming model designed to optimize dietary astaxanthin concentrations throughout the grow-out period that results in well-pigmented fish at minimum cost. We have applied a mixed-integer non-linear programming algorithm to solve this problem. Various managerial implications of applying optimization models in product quality management of farmed salmon are discussed.     

Astaxanthin deposition in fillets of Atlantic salmon Salmo salar L. fed two dietary levels of astaxanthin in combination with three levels of α-tocopheryl acetate

The influence of α-tocopheryl acetate (α-TOAc) on plasma concentration and fillet deposition of dietary astaxanthin was investigated in Atlantic salmon Salmo salar L. The diets were added 30 or 50 mg kg^–1 astaxanthin, and 200, 400 or 800 mg kg^–1α-TOAc at each astaxanthin level. Improved flesh deposition of astaxanthin by 8–14% was achieved for fish fed diets with 30 and 50 mg kg^–1 astaxanthin, respectively, by the dietary addition of 800 compared with 200 mg kg^–1α-TOAc. These results were supported by CIE[1976]L*a*b* tristimulus redness measurements (a* value). Plasma astaxanthin concentration mirrored the muscle astaxanthin concentration in the groups of fish fed a diet containing 30 mg kg^–1 astaxanthin. The salmon fed a high astaxanthin and low α-TOAc diet had the highest plasma concentration of idoxanthin (P < 0.05). Astaxanthin retention was significantly higher (P < 0.001) in salmon fed 30 mg kg^–1 astaxanthin than in those fed 50 mg kg^–1 astaxanthin, but was not significantly affected by dietary α-TOAc. Liver weight, body weight, specific growth rate, feed/gain ratio and mortalities were not affected by dietary α-TOAc levels. In conclusion, the dietary addition of α-TOAc appears to increase astaxanthin fillet deposition in salmonids and may reduce the demand for astaxanthin supplementation. The effect was rather small and requires verification.     

Assessment of flesh colour in Atlantic salmon, Salmo salar L.

The degree of pigmentation in muscle of Atlantic salmon, Salmo salar L., fillets of fish that were fed eight diets fortified with 10, 20, 40, 60, 80.100, 150 and 200 mg astaxanthin kg^?1 and a non-supplemented control diet from 3 to 21 months was assessed using different methods. A tristimulus colorimeter (Minolta Chroma Meter) was used to measure the colour composition of the fillets instrumentally. The colour was also determined using the Roche Colour Card for Salmonids. The concentration of astaxanthin in the muscle was measured by chemical analyses. All measurements for colour were done directly on the epaxial muscle anterior to the dorsal fin. The lightness factor (L *). the red/green chromaticity (a*), the yellow/blue chromaticity (b*) and the saturation C* of the colorimetric readings and the Colour Card scores were compared with the chemical analyses. The astaxanthin concentration in the flesh varied from 1 to 10 mg kg^?1 and the visual appearance of the fillets varied from yellowish-white to red. The relationship between the a*, b* and C* values and the astaxanthin concentration in the muscle was non-linear. Non-linear regression lines were found between the a* value and the astaxanthin concentration in the flesh (r²= 0.974) and the b* value and the astaxanthin concentration in the flesh (r²= 0.984). The instrument was not able to detect differences in astaxanthin concentration at astaxanthin levels above 3-4 mg kg^?1 using the presented method directly on the fillet. The instrument might be useful for rejecting groups of salmon with poor pigmentation. A good linear regression was found between the Colour Card score and the mean astaxanthin concentration in the flesh (r² - 0.992). The Colour Card provided a better prediction of the astaxanthin concentration at higher astaxanthin levels than the Chroma Meter. None of the methods provided a satisfactory prediction of the astaxanthin concentration in the muscle of individual fish using the presented methods.     

Deposition of astaxanthin in fillets of Atlantic salmon (Salmo salar) fed diets with herring, capelin, sandeel, or Peruvian high PUFA oils

To elucidate whether absorption and deposition of dietary astaxanthin are influenced by the use of different dietary fish oils having different melting points and fatty acid profiles, triplicate groups of individually labeled Atlantic salmon (initial average weight 569 g) were reared in 2 m² tanks, supplied with saltwater. The fish were fed four different experimental diets coated with either herring oil, capelin oil, sandeel oil, or a Peruvian oil high in polyunsaturated fatty acids. Salmon fed diets containing Peruvian high PUFA oil had significantly higher (13%) fillet carotenoid content than salmon fed herring oil (P<0.05). Astaxanthin retention was significantly higher (P<0.05) in salmon fed capelin and Peruvian high PUFA oil than in the two other groups. The effects of dietary oil supplements on carotenoid deposition were rather small and require verification. Redness of fillets and blood plasma astaxanthin levels did not differ among treatments. Liver weights, body weights, as well as specific growth rates, and feed conversion ratios were unaffected by dietary oil source. Significant (P<0.05) positive linear relationships were found between final fillet idoxanthin concentration and total saturated fatty acids in supplement oils, astaxanthin and total monounsaturated fatty acids, and redness and total n−3 fatty acids, whereas the relationships between redness and total monounsaturated fatty acids and astaxanthin and total n−3 fatty acids were negative.     

Effect of dietary bile extracts on serum response of astaxanthin in rainbow trout (Oncorhynchus mykiss): a preliminary study

Effects of porcine bile extracts added at three different dietary concentrations 0, 10 and 20 g kg^?1 were studied on astaxanthin serum concentration in rainbow trout (mean weight 200 ± 7 g). Astaxanthin from micro‐algae Haematococcus pluvialis and synthetic astaxanthin (CAROPHYLL® pink) were incorporated in diets of rainbow trout at a rate of 100 mg astaxanthin kg^?1 of feed. Fish were hand fed twice a day. After 5 days of feeding there was a significant effect of the pigment source on the ratio (total blood astaxanthin per unit body weight to cumulative astaxanthin intake per unit body weight). Trout receiving synthetic astaxanthin showed a significantly (P < 0.05) higher ratio than trout fed algal astaxanthin. Increasing dietary bile extract did not lead to produce any effect on this ratio. The power of the statistical analysis is discussed. Therefore, the interaction (pigment source × dietary bile concentration) showed no more effect.     

Carotenoid deposition in pen-reared salmonids fed diets containing oil extracts of red crab (Pleuroncodes planipes)

The rate of deposition of carotenoids in pen-reared coho salmon was investigated by the addition of known carotenoid levels to diets. The carotenoids added to the diets were derived from red crab (P. planipes), and a process is described for the preparation of a soya oil carotenoid concentrate. Using a 3-stage counter-current extraction process, extracts containing 155 mg/100 g oil were prepared from red crab (P. planipes). Oregon moist pellets containing 3, 6, and 9 mg carotenoid/100 g were prepared using these extracts and were fed to coho salmon (Oncorhynchus kisutch) for 120 days. The amount of carotenoid deposited in the flesh of the fish was related to the carotenoid content of the diet and to the weight of the fish. Fish fed diets containing 6 and 9 mg carotenoid/100 g for the same length of time contained 60% more flesh carotenoids than those fed 3 mg/100 g. In general, after 120 days of feeding, only those fish feeding on diets containing 6.0 and 9.0 mg carotenoid/100 g and weighing over 215 g were assessed as having good-to-excellent coloration. Analysis of the flesh showed that there was no correlation between its carotenoid and fat contents.     

The effect of synthetic and natural pigments on the colour of the cichlids (<Emphasis Type="Italic">Cichlasoma severum</Emphasis> sp., Heckel 1840)

In this study, we have investigated the effects of Porphyridium cruentum (Rodophyta) as a natural pigment source and astaxanthin and β-carotene as synthetic pigment sources on the skin colour of cichlid fish (Cichlasoma severum sp., Heckel 1840), which are generally light orange with white patches and becomes shiny orange in the reproductive phase. The fish were fed diets containing 50 mg kg⁻¹ astaxanthin and β-carotene, and P. cruentum powder. The amount of both natural and synthetic pigment sources given as feed was 50 mg kg⁻¹, and the experiment was continued for 50 days. Total carotenoid content of the fish was determined spectrophotometrically at the end of the experiment. As a result, while a visible change of colour in the skin of the fish fed on the feed containing astaxanthin was observed with 0.34 ± 0.2 mg g⁻¹ of pigment accumulation, a relatively small change of colour was observed in the skin of other fish that were fed on the feed containing P. cruentum and β-carotene with 0.22 ± 0.2 mg g⁻¹ and 0.26 ± 0.1 mg g⁻¹ of pigment accumulations, respectively. Therefore, it was determined that these pigment sources have an effect on the colour of cichlid fish.     

Effects of feeding diets containing various dietary protein and lipid ratios on the growth performance and pigmentation of post-juvenile coho salmon Oncorhynchus kisutch reared in sea water

Six extruded dry diets formulated to contain one of two levels of digestible protein (37% or 44%) and one of three levels of digestible lipid (16%, 23% or 30%) on a dry weight basis and a seventh diet (commercial control) were used to feed triplicate groups of post‐juvenile coho salmon Oncorhynchus kisutch in sea water. Fish were fed to satiation twice daily for 168 days. Growth performances were monitored every 28 days. On day 168, samples were taken from each replicate group per dietary treatment for determinations of whole‐body and muscle proximate compositions. Fatty acid compositions and astaxanthin concentration in both the experimental diets and fish flesh were assessed by gas chromatography (GC) and high‐performance liquid chromatography (HPLC) respectively. Coho salmon fed diets containing the higher lipid levels (23–30%) exhibited improved feed efficiency, protein efficiency ratio, percentage protein deposition and percentage gross energy utilization. Higher protein content diets supported better growth than those that had lower protein content, but the former led to lowered protein efficiency ratio, percentage protein deposition and gross energy utilization. Fish fed the diets with high lipid levels (23% or 30%) also had higher astaxanthin content in raw flesh.     

The influence of dietary astaxanthin and temperature on flesh colour in Arctic charr Salvelinus alpinus L.

Arctic charr Salvelinus alpinus L. averaging 150 g were fed six diets containing from 0 to 192 mg astaxanthin per kilogram dry diet al two temperatures (8 C and 12 C), After reaching an average weight of 320 g (102 days at 12 C and 126 days at 8 C), the fish were killed for evaluation of flesh pigmentation using instrumental colour measurement. There was a positive relationship between dietary astaxanthin and muscle redness up to a dietary concentration of around 70 mg kg^-1, where a plateau in pigmentation was reached. Tail sections were more intensely pigmented compared with the neck and dorsal regions. Within each temperature regime, flesh coloration was positively correlated to specific growth rate. Fish maintained at 8 C had significantly higher pigmentation compared to those grown at 12 C.     

不同脂肪源日粮补充维生素E对罗氏沼虾生长、免疫及肉品质的影响

本研究旨在完善罗氏沼虾（）饲料配方,降低罗氏沼虾饲料成本。研究采用3×2双因素设计,配制6组饲料,分别包含鱼油（fish oil,FO）、豆油（soybean oil,SO）、菜籽油（rapeseed oil,RO）三种脂肪源;200 mg/kg（200VE）和600 mg/kg（600VE）两个维生素E（VE）水平。养殖实验在温室水泥池中进行,每个处理3个重复,养殖期8周,每天定点定量投喂3次。结果显示,相对于FO组,SO和RO组增重率、特定生长率显著升高,饵料系数显著下降（>0.05）。对于血淋巴抗氧化指标,在相同VE水平下,FO组血淋巴总抗氧化能力（T-AOC）和超氧化物歧化酶（SOD）活性均显著低于SO和RO组,谷胱甘肽过氧化物酶（GPX）活性均显著高于SO和RO组（<0.05）。在相同脂肪源下,600VE可显著提高FO组T-AOC活性,RO组GPX活性以及SO和RO组SOD活性（>0.05）。对于血淋巴生理生化指标,谷草转氨酶（AST）、总蛋白（TP）、白蛋白（ALB）和甘油三酯（TC）受日粮影响显著（<0.05）。此外,日粮脂肪源和VE水平对肉质也有显著影响。其中,SO组肌肉鲜度和滋味强度较高;RO组鱼腥味较低;FO组肌肉亮度较高,气味强度较低。在200 mg/kg VE水平下,FO组肌肉硬度、胶黏性、耐咀性、黏性和回复性显著高于植物油组（<0.05）,而对肌肉蒸煮损失和滴水损失无显著影响（>0.05）。上述结果表明,相对于鱼油,豆油和菜籽油等植物油是罗氏沼虾更优质的脂肪源,VE在以鱼油为单一脂肪源的饲料中有一定的促生长和缓解应激的作用,且脂肪源和VE均显著影响肌肉品质。本研究结果将为降低鱼油在罗氏沼虾饲料中的使用提供数据支持。     

Efficacy of an equal blend of canola oil and poultry fat as an alternate dietary lipid source for Atlantic salmon (Salmo salar L.) in sea water. I: effects on growth performance, and whole body and fillet proximate and lipid composition

This study assessed the suitability and cost efficacy of an equal blend of canola oil (CO) and poultry fat (PF) as a supplemental dietary lipid source for juvenile Atlantic salmon. Quadruplicate groups of Atlantic salmon (～400 g) held in 4000 L outdoor fibreglass tanks supplied with running (35–40 L min^?1), aerated (dissolved oxygen, 7.88–10.4 mg L^?1), ambient temperature (8.6–10.9°C) sea water (salinity, 26–35 g L^?1) were fed twice daily to satiation one of three extruded dry pelleted diets of equivalent protein (488–493 g kg^?1 dry matter) and lipid (267–274 g kg^?1 dry matter) content for 84 days. The diets were identical in composition except for the supplemental lipid (234.7 g kg^?1) source viz., 100% anchovy oil (AO; diet COPF‐0), 70.2% AO and 29.8% CO and PF (diet COPF‐30), and 40.3% AO and 59.7% CO and PF (diet COPF‐60). Atlantic salmon growth rate, feed intake, feed efficiency, protein and gross energy utilization, percent survival and whole body and fillet proximate compositions were not affected by diet treatment. Cost per kilogram weight gain was about 10% less for fish fed diet COPF‐60 than for diet COPF‐0. Percentages of saturated fatty acids in dietary and fillet lipids varied narrowly. Moreover, percentages of 18:1n‐9, monounsaturated fatty acids, 18:2n‐6, n‐6 fatty acids, 18:3n‐3, and ratios of n‐6 to n‐3 fatty acids in the flesh lipids were directly related to the dietary level of CO and PF whereas 22:6n‐3, the total of 20:5n‐3 (eicosapentaenoic acid; EPA) and 22:6n‐3 (docosahexaenoic acid; DHA), and n‐3 fatty acids revealed the opposite trend. Percentages of 22:6n‐3, EPA and DHA, and n‐3 fatty acids were significantly depressed in fish fed diet COPF‐60 versus diet COPF‐0. We conclude that a 1:1 blend of CO and PF is an excellent cost‐effective dietary source of supplemental lipid for Atlantic salmon in sea water.     

Protein from Northern krill (Thysanoessa inermis), Antarctic krill (Euphausia superba) and the Arctic amphipod (Themisto libellula) can partially replace fish meal in diets to Atlantic salmon (Salmo salar) without affecting product quality

The main objective of the present study was to evaluate the effect of using three different crustacean meals (Tysanoessa inermis, Euphausia superba, Themisto libellula) on product quality of Atlantic salmon (Salmo salar L.). In order to do this, a total of six iso‐protein, iso‐lipid and iso‐carotenoid diets were prepared. Two experimental diet series were prepared. In the first series, a control feed (K0) was compared with diets where 20%, 40% and 60% of the fish meal protein were replaced with protein from Northern krill T. inermis (K20, K40 and K60, respectively). In the second series, control feed (K0) was compared with diets where 40% of the dietary protein was replaced by protein from T. inermis (K40), Antarctic krill E. superba (AK40) and the Arctic amphipod T. libellula (AMP40). The salmon groups were fed the various diets for 160 days and the average weight of the fish increased from 410 g to around 1500 g. Fish given diets containing krill displayed a general better growth compared with the ones given pure fish meal diet. Replacing fish meal protein with protein from the crustacean sources had, in general, only minor effects on the flesh quality measured both by technical and sensory methods. However, some significant effects were noted. Postmortem muscle pH was generally lower (P < 0.05), for K20, K40, AMP40 in fish fed crustacean diets compared with those receiving the control diet. Increasing the replacement level of non‐fish meal protein from Northern krill (K20, K60) significantly reduced the rigor contraction. Fish given K20 had a slightly firmer meat texture, measured as resistance to post‐rigor compression, especially when compared with K60 (P < 0.05). Fish from the K20 and AMP40 groups had a deeper red flesh coloration [both light reflection (A*‐value and chroma) and flesh astaxanthin concentration] than fish fed K0 and higher inclusions of krill meal. The groups with the highest astaxanthin flesh content also showed the best growth and had the highest feed intake. Finally, a sensory panel analysis differed slightly from the technical measurements in that K0, rather than K20 was given the highest score for hardness and colour. In comparison with K0, AK40 got the lowest salty taste and hardness scores from the panellists relative to the control fish (P < 0.05). Despite minor effects on the present quality measures, it is concluded that meal from three different crustacean species can successfully replace fish meal up to 60% with Northern krill, and 40% of Antarctic krill and amphipod meal of dietary proteins.     

Intestinal absorption of astaxanthin, plasma astaxanthin concentration, body weight, and metabolic rate as determinants of flesh pigmentation in salmonid fish

Experiments were conducted to determine whether poor intestinal absorption of astaxanthin or some other metabolic factor is primarily responsible for pigmentation failure in white chinook salmon and small juvenile fish of other salmonid species. None of the fish studied failed to absorb astaxanthin from a single oral dose of the pigment. Intensity of flesh pigmentation in coho ranging in weight from 30–400 g, and fed a diet supplemented with astaxanthin, was significantly correlated with body weight. There was no correlation, however, between flesh colour and plasma astaxanthin concentration or between body weight and plasma astaxanthin concentration. Dietary triiodothyronine reduced both flesh pigmentation and plasma astaxanthin. It is concluded that poor flesh pigmentation results from rapid metabolism of absorbed pigment to colourless derivatives rather than from failure of the fish to absorb pigment.     

The effect of three carotenoid sources on growth and pigmentation of juvenile freshwater crayfish Cherax quadricarinatus

The effect of adding carotenoids from various sources to feed of juvenile freshwater crayfish Cherax quadricarinatus on pigmentation, growth and survival was examined under laboratory conditions. Juvenile crayfish were fed diets fortified with carotenoids at a level of 100 μg g⁻¹ for a period of either 49 or 55 days. Carotenoid sources were: dried algal cells prepared from Dunaliella salina in which the main carotenoid is β-carotene; a synthetic carotenoid, astaxanthin (Carophyll Pink 8%, manufactured by Hoffman–La Roche) and alfalfa meal. Crayfish receiving feeds fortified with carotenoids exhibited better body colouration than those in the control group, which were fed a diet to which no carotenoids were added. Growth and survival of the crayfish were not affected by the addition of carotenoids to their diet.     

Natural bixin as a potential carotenoid for enhancing pigmentation and colour in goldfish (Carassius auratus)

Discovering natural carotenoids for colour enhancement and health benefits of fish is important to develop new feed formulations. We have purified natural bixin from achiote seeds and evaluated the effect of colour enhancing and pigmentation in goldfish. Varying levels of bixin‐based diets were prepared with 420 g kg^?1 of crude protein and 120 g kg^?1 of lipid content. Our results clearly showed that bixin (0.05, 0.10, 0.20 and 0.60 g kg^?1) based diets significantly (P < 0.05) enhanced the skin and fin colour at 30 and 60 days compared to diet without bixin. Interestingly, diet which contains 0.20 g kg^?1 bixin and commercial feed (with astaxanthin) had similar effect on carotenoid deposition in skin. Moreover, total carotenoid deposition in fin was higher than in skin of all bixin‐containing diets. However, 0.60 g kg^?1 bixin‐containing diet had lower specific growth rate (1.01 ± 0.01) and higher feed conversion ratio (2.05 ± 0.19) compared to the control group. The present results demonstrate that achiote bixin can be successfully used as an alternative natural carotenoid source against synthetic astaxanthin in fish feed. Our data indicate that 0.20 g kg^?1 is a suitable dietary level of bixin to ensure strong pigmentation, acceptable growth and feed utilization in goldfish.     

Dorsal aorta cannulation: a method to monitor changes in blood levels of astaxanthin in voluntarily feeding Atlantic salmon, Salmo salar L.

This study was undertaken to assess dorsal aorta cannulation as a method to evaluate alterations in diet composition and feeding protocol on pigment retention in salmonid fish. Temporal changes in blood astaxanthin concentrations of dorsal aortacannulated Atlantic salmon, Salmo salar L., were followed in relation to variations in dietary pigment concentration and fish-feeding husbandry protocol. The fish were held individually in 200-L fibreglass tanks supplied with running sea water. Each fish was forced to swim at 0.5 body lengths s^?1 and was fed daily by hand to satiation. The fish had an average growth rate of 1% day^?1. Blood astaxanthin concentrations were noted to be highly correlated (r= 0.995) with dietary levels of astaxanthin, but not as well correlated (r= 0.71) with total gut content of this pigment. Marked variations in blood astaxanthin concentration were noted between individual fish at each dietary pigment concentration, but the ranking of the fish was generally unaffected between each dietary pigment level. After cessation of feeding a diet supplemented with 75 mg of astaxanthin kg^?1, salmon fed a diet with no pigment showed more-rapid blood pigment clearance than those that were starved. Likely, feed remaining in the alimentary tract of the starved fish functioned as a reservoir of pigment for the blood until the intestinal tract was empty. Blood pigment levels were not depressed in salmon fed a diet supplemented with 75 mg of astaxanthin kg^?1 once daily instead of twice daily.