Feedipedia
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Feedipedia
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Fish meal

Datasheet

Description
Click on the "Nutritional aspects" tab for recommendations for ruminants, pigs, poultry, rabbits, horses, fish and crustaceans
Common names 

Fish meal, fishmeal, brown fish meal, white fish meal, low-temperature (LT) fish meal, prime fish meal [English]; harina de pescado [Spanish]; farinha de peixe, farinha de pescado [Portuguese]; farines de poisson [French]; Fischmehl [German]; farina di pesce [Italian]; 魚粉 [Chinese]; Рыбная мука [Russian]

Description 

Fish meal is a protein-rich feed ingredient obtained by cooking, pressing, drying and milling whole fish or fish processing by-products (FAO, 2025; Nguyen et al., 2022). It is produced from small pelagic fish caught for the manufacture of fish meal and fish oil, such as anchovy, menhaden, sardine, capelin, herring and similar species, and from fish processing by-products including heads, frames, viscera, skin and trimmings (FAO, 2025; Love et al., 2024). The relative contribution of whole fish and by-products varies between countries, fisheries and processing industries, and the use of by-products has increased as a way to improve resource efficiency (FAO, 2025; Love et al., 2024).

Fish meal is generally a brown to greyish-brown powder or granular product with a characteristic marine odour (FAO, 2025; Cho et al., 2011). Its colour, texture and smell depend on the fish species used, the freshness of the raw material, the lipid content, the drying process and storage conditions (Mih et al., 2020; Nguyen et al., 2022). Good quality fish meal is usually palatable and highly digestible, whereas poor-quality meals may have rancid, burnt or putrid odours, or show signs of deterioration, oxidation or heat damage (Mih et al., 2020; Nguyen et al., 2022).

Fish meal is valued in animal feeding as a concentrated marine protein source combining high digestibility, a favourable amino acid profile, minerals, residual marine lipids and palatability (Cho et al., 2011; FAO, 2025). However, it should not be considered as a single uniform ingredient, but as a group of marine protein meals whose composition and feeding value depend on raw material origin and processing quality (Cho et al., 2011; Love et al., 2024; Nguyen et al., 2022).

Fish meal should be distinguished from related marine feed ingredients such as fish protein concentrate, fish protein hydrolysate, fish silage, fish solubles and fish oil (FAO, 2025). These products may share the same raw materials but differ in processing method, physical form, composition, digestibility, palatability and practical use in animal feeds (FAO, 2025; Nguyen et al., 2022).

Commercial grades and quality denominations

Fish meal is commonly traded under commercial denominations that indicate broad quality levels, although these names are not fully standardised between origins, suppliers and markets. Standard or FAQ (fair average quality) fish meal generally refers to ordinary fish meal, often around 64-67% crude protein, with higher variability in freshness, ash content and amine levels than premium products. Prime, Super Prime, Special or high-protein fish meal usually refers to meals made from fresher raw material, with higher protein content, often about 68-72%, lower ash and lower biogenic amine levels. These grades are mainly used in aquafeeds, piglet feeds and other high-value diets where digestibility, palatability and freshness are critical (IFFO, 2026; Feedipedia, 2026).

Other commercial names describe processing or raw material rather than a formal grade. LT fish meal, or low-temperature fish meal, generally indicates a meal dried under milder conditions to preserve protein quality and amino acid digestibility. Steam-dried or indirectly dried fish meal is often preferred to flame-dried meal when heat damage must be minimised. White fish meal is usually produced from lean white fish or white fish processing by-products and is paler and often lower in lipid than oily-fish meals, but its nutritional value still depends on protein, ash and freshness. By-product fish meal or low-protein fish meal may contain more heads, frames and bones, resulting in higher ash and mineral contents but lower protein and energy concentration (Feedipedia, 2026; Nguyen et al., 2022).

Commercial denominations should be used only as preliminary indicators. In diet formulation and feed purchasing, fish meal quality should be checked through analytical specifications such as crude protein, ash, moisture, lipid content, salt, amino acid profile, digestibility, freshness indicators, oxidation status and contaminant control. A named grade such as Prime, Super Prime, FAQ or LT does not guarantee feeding value unless it is supported by analytical data and reliable origin and processing information (Cho et al., 2011; Mih et al., 2020; Nguyen et al., 2022).

Distribution 

Production and market

Fish meal is a globally traded feed ingredient whose supply is structurally limited by the availability of capture fisheries, fisheries management rules, climate variability and the increasing use of fish for direct human consumption (FAO, 2025; OECD-FAO, 2025). Fish processing by-products can improve resource efficiency, but their availability, quality and logistics vary between countries and value chains (FAO, 2025; Love et al., 2024). Their use depends on scale, seasonality, transport distance, processing capacity and the economic value of rendering compared with alternative uses or disposal (Love et al., 2024).

Global fish meal production is expected to remain in the range of about 5-6 million t/year (OECD-FAO, 2025). The OECD/FAO outlook projects global fish meal production at 5.9 million t by 2034, and fish oil production at 1.5 million t (OECD-FAO, 2025). It also projects that about 31% of fish meal will come from waste and by-products by 2034, compared with 29% in the 2022-2024 base period (OECD-FAO, 2025).

Aquaculture remains the main outlet for fish meal, and its share of fish meal use is projected to rise from 78% in the base period to 84% by 2034 (OECD-FAO, 2025). The fish meal market remains volatile because a large part of the supply depends on a limited number of small pelagic fisheries, especially the Peruvian anchoveta fishery (FAO GLOBEFISH, 2025; OECD-FAO, 2025). Higher catches in Peru increased global supplies in 2025, and FAO GLOBEFISH reported that Peruvian fish meal exports reached 421,000 t in the first quarter of 2025, 67% more than in the same period of the previous year (FAO GLOBEFISH, 2025). This dependence on a limited and variable supply makes fish meal a high-value and supply-sensitive ingredient rather than a routine bulk protein commodity (Kaushik, 2010; FAO GLOBEFISH, 2025; OECD-FAO, 2025).

Processes 

Fish meal is generally manufactured by cooking, pressing, drying and milling whole fish or fish processing by-products (FAO, 2025; Nguyen et al., 2022). Cooking coagulates proteins and releases water and oil, and the cooked material is pressed to produce a solid press cake and a liquid phase (Nguyen et al., 2022). The liquid phase is separated into fish oil and stickwater, the latter being concentrated and usually added back to the press cake before drying (Nguyen et al., 2022). The dried product is then milled and stabilised for storage (FAO, 2025; Nguyen et al., 2022).

The basic process has changed little, but modern processing aims to preserve protein quality, maintain digestibility, reduce lipid oxidation and control undesirable nitrogenous compounds (Nguyen et al., 2022). Fish meal quality is strongly affected by the freshness and species of the raw material, the delay before processing, the conditions of cooking and drying, and the handling of liquid streams (Mih et al., 2020; Nguyen et al., 2022). During industrial processing, chemical composition changes at each step, and non-protein nitrogen compounds such as biogenic amines, total volatile basic nitrogen, trimethylamine and dimethylamine tend to follow the liquid streams, which means that stickwater handling can influence the quality of the final product (Nguyen et al., 2022).

Good quality fish meal is characterised by a high crude protein content, high amino acid availability, moderate ash content, controlled moisture, low lipid oxidation and low levels of biogenic amines (Cho et al., 2011; Mih et al., 2020; Nguyen et al., 2022). High-protein fish meals generally have lower ash and higher digestibility, whereas meals produced from mixed by-products or poorly selected raw material may contain more ash and less protein (Kaushik, 2010; Cho et al., 2011; Love et al., 2024). Low-temperature and steam-dried meals are generally preferred when high digestibility and minimal heat damage are required (Cho et al., 2011; Nguyen et al., 2022).

Environmental impact 

The environmental impact of fish meal is context-dependent. It depends on the fish species used, the status and management of the fisheries, the proportion of processing by-products, fuel use during fishing, processing efficiency, allocation rules in life cycle assessment, and the efficiency with which fish meal is used in animal production systems. Fish meal produced from managed reduction fisheries can support important regional economies and provide a concentrated, stable and highly digestible feed ingredient for aquaculture and livestock. Fish meal produced from processing by-products can also improve resource use by recovering nutrients from material that may otherwise have limited value or create disposal problems (FAO, 2025; Love et al., 2024; Majluf et al., 2024).

The main environmental and food-system questions arise when fish meal is produced from whole small pelagic fish. These fish may have several possible roles: they can support reduction fisheries and export income, supply local or regional food markets, contribute to marine food webs, or be used indirectly through aquaculture and livestock feeds. The relative importance of these roles differs between countries, fisheries and markets. The environmental assessment of fish meal should therefore consider fisheries management, local livelihoods, food security, ecosystem functions and the nutritional value obtained from its final use, rather than assuming that one use is always preferable to another (FAO, 2025; Majluf et al., 2024).

In aquaculture, fish meal inclusion rates have decreased substantially while total production has continued to increase. FAO reports that the proportion of fish meal in aquafeeds declined from 19% in 2000 to 9% in 2020, reflecting improvements in formulation, amino acid balancing and the use of alternative protein sources. However, absolute demand remains high because aquaculture continues to expand, and fish meal remains useful in carnivorous species, young stages and demanding feeds where it provides digestible protein, palatability, minerals and functional compounds (FAO, 2025; OECD-FAO, 2025; Glencross et al., 2024b).

Fish-in:fish-out (FIFO) indicators are useful to describe the dependence of aquaculture on wild fish resources, but they are sensitive to assumptions about fish meal and fish oil yields, inclusion rates, feed conversion ratios and the treatment of by-products. Fish oil is particularly important because its yield is lower and more variable than that of fish meal, and it may drive marine-resource dependency in some carnivorous aquaculture systems. Life cycle assessment data from Peru reported about 320 kg CO2-eq per t of fish meal and 4430 kg CO2-eq per t of fish oil under energy allocation, with the fishery stage accounting for about 45% of greenhouse gas emissions. These figures show that carbon footprint is only one part of the assessment, which also includes fisheries management, ecosystem effects, by-product recovery, food-feed interactions and the socio-economic role of reduction fisheries (Deville et al., 2025; Glencross et al., 2024a; Majluf et al., 2024).

Nutritional aspects
Nutritional attributes 

Fish meal is a concentrated source of high-quality protein, digestible amino acids, minerals and energy, but its feeding value varies markedly with protein and ash contents, raw material origin and processing quality (Feedipedia, 2026; Cho et al., 2011). High-protein fish meal contains about 75% crude protein and 14% ash on a dry matter basis, whereas standard fish meal contains about 71% crude protein and 18% ash, and low-protein fish meal may contain less than 50% crude protein and more than 35% ash (Feedipedia, 2026).

Its amino acid profile is favourable, with high levels of lysine, methionine, threonine, leucine and valine relative to crude protein, which explains its value in young animals, poultry and aquaculture feeds where high digestibility, palatability and balanced essential amino acids are required (Feedipedia, 2026; Cho et al., 2011).

Fish meal is also rich in calcium and phosphorus, but high mineral content usually indicates more bones, heads or frames and is associated with lower protein and energy concentration (Feedipedia, 2026). Energy value and digestibility decline as ash content increases, while moderate rumen degradability and high intestinal digestibility explain its historical use as a source of rumen-undegradable protein in ruminants (Feedipedia, 2026; Hussein et al., 1991).

Overall, fish meal should not be treated as a uniform ingredient. For diet formulation, it should be evaluated according to crude protein, ash, lipid content, amino acid profile, digestibility, energy value, mineral contribution and quality indicators rather than by name alone (Cho et al., 2011).

Potential constraints 

Variability and quality control

Fish meal is a variable ingredient whose protein, ash, lipid content, amino acid availability and mineral content depend on the species processed, the proportion of whole fish and by-products, the freshness of the raw material and the processing conditions (Cho et al., 2011; Love et al., 2024; Nguyen et al., 2022). High ash levels may indicate a high proportion of heads, frames or bones, while excessive heat treatment may reduce amino acid availability (Cho et al., 2011; Nguyen et al., 2022). For animal feeding, fish meal should therefore be purchased on the basis of specifications including crude protein, ash, moisture, lipid content, freshness indicators, digestibility and contaminant status (Cho et al., 2011; FAO, 2025; Nguyen et al., 2022).

Biogenic amines and histamine

Fish proteins and non-protein nitrogen compounds are prone to degradation when raw material is not processed rapidly or adequately preserved (Mih et al., 2020; Nguyen et al., 2022). Biogenic amines, particularly histamine, are among the main quality risks in fish meal made from deteriorated raw material, and histamine content in the final meal is strongly influenced by raw material freshness (Mih et al., 2020; Nguyen et al., 2022). In one study, when raw material freshness remained acceptable, with total volatile basic nitrogen around 30 mg/100 g, histamine levels in the finished fish meal remained below the 500 ppm limit used by the authors (Mih et al., 2020).

Lipid oxidation

Fish meal contains residual lipids rich in long-chain polyunsaturated fatty acids, which are susceptible to oxidation (Cho et al., 2011; FAO, 2025). Oxidised lipids can reduce palatability, impair nutrient value and contribute to poor animal performance or product quality (Cho et al., 2011; FAO, 2025). This risk increases when fish meal is made from fatty raw material, poorly stabilised, stored for long periods, exposed to heat and oxygen, or transported under poor conditions; antioxidant treatment, appropriate moisture control and dry, cool storage are therefore important for maintaining quality (FAO, 2025; Nguyen et al., 2022).

Gizzerosine and heat damage

Overheating during drying may promote the formation of gizzerosine, a compound derived from histamine (Jiao et al., 2024). Gizzerosine is particularly important in poultry because it can cause gizzard erosion and black vomit (Jiao et al., 2024). The risk is associated with excessive heat treatment and poor control of drying conditions, and recent work confirms that detection methods and control of heat damage remain important in animal feed matrices (Jiao et al., 2024; Nguyen et al., 2022).

Persistent contaminants

Fish meal may contain persistent environmental contaminants such as dioxins, dioxin-like PCBs, non-dioxin-like PCBs and some heavy metals (EFSA CONTAM Panel, 2026; FAO, 2025). Their levels depend on fish species, fishing area, trophic level, lipid content and processing (EFSA CONTAM Panel, 2026; FAO, 2025). These contaminants are relevant because fish meal can transfer contaminants into animal products when inclusion rates are high or when contaminated lots are used, and EFSA's 2026 update confirms that dioxins and dioxin-like PCBs remain a food and feed safety concern (EFSA CONTAM Panel, 2026).

Microbial contamination and storage

Cooking generally destroys most microorganisms present in the raw material, but recontamination may occur during drying, cooling, milling, storage or transport (FAO, 2025; Nguyen et al., 2022). Low moisture limits bacterial growth, but contaminated storage buildings, condensation, rodents, birds, insects or poor handling may compromise product safety (FAO, 2025). Fish meal should be stored dry and protected from moisture, heat and contamination (FAO, 2025).

Palatability and product taint

Fish meal is usually palatable, especially for young animals and aquatic species, but excessive inclusion or poor-quality meal may cause undesirable odours or fishy taints in animal products, particularly eggs and meat (Cho et al., 2011; FAO, 2025). This risk is influenced by inclusion level, lipid quality, freshness, species, feed withdrawal before slaughter or egg marketing, and the sensitivity of the target market (Cho et al., 2011; FAO, 2025).

Cost, availability and regulatory constraints

The use of fish meal is limited by price, variable availability and competition from aquaculture, piglet feeds, poultry feeds, pet food and other high-value markets (FAO, 2025; OECD-FAO, 2025). In ruminant nutrition, regulatory restrictions are a major constraint in several regions (European Commission, 2001; European Commission, 2013; Animal Health Australia, 2026). In the European Union, Regulation (EC) No 999/2001 prohibits feeding ruminants with protein derived from animals, with tightly defined derogations, while Regulation (EU) No 56/2013 authorises fish meal for unweaned ruminants only in milk replacers under specific conditions (European Commission, 2001; European Commission, 2013; European Commission, 2021). Australia applies an inclusive ruminant feed ban covering meals derived from vertebrates, including fish and birds (Animal Health Australia, 2026).

Ruminants 

Fish meal is a nutritionally valuable but now rarely routine ingredient in ruminant feeding. It has been used as a source of high-quality rumen-undegradable protein and digestible amino acids, particularly in high-producing dairy cows, young growing animals and diets based on medium- or poor-quality forages. However, its practical use is now strongly limited by regulation, cost, availability and competition from other protein sources or protected amino acids. It should therefore be considered only where it is legally permitted and where a specific need for high-quality undegradable protein has been identified (Hussein et al., 1991; Santos et al., 1998; European Commission, 2013).

Fish meal has historically been used in ruminant diets as a source of high-quality rumen-undegradable protein, because processing reduces ruminal protein degradation while maintaining a high intestinal digestibility of amino acids (Hussein et al., 1991; González et al., 1998; Yoon et al., 1998). Its value is mainly related to the supply of metabolizable protein and essential amino acids, particularly lysine and sulphur-containing amino acids, in diets where microbial protein and rumen-degradable protein do not fully meet animal requirements (Santos et al., 1998; Korhonen et al., 2002).

The response to fish meal supplementation has been variable and depends on the basal diet, forage quality, production level, physiological stage and the balance between rumen-degradable and rumen-undegradable protein (Hussein et al., 1991; Santos et al., 1998). Fish meal was more likely to improve performance when it supplemented medium- or poor-quality forages, high-forage diets, early lactation cows, young growing ruminants or diets deficient in metabolizable protein or amino acids (Hussein et al., 1991; Schroeder et al., 2000; Korhonen et al., 2002). In dairy cows, fish meal has been reported to improve amino acid supply, milk yield or milk protein yield in some experiments, but low inclusion levels or well-balanced diets did not always result in measurable benefits (Allison et al., 2002; Korhonen et al., 2002; Schroeder et al., 2000).

The practical value of fish meal in ruminants is now much more limited than its nutritional value would suggest. In many production systems, its use has been reduced by high price, limited availability, competition with aquaculture and monogastric feeds, and the availability of alternative sources of rumen-undegradable protein or protected amino acids (Santos et al., 1998; Allison et al., 2002). In sheep, fish meal has also been used as a source of undegradable protein, particularly in late pregnancy, lactation or early-weaned lambs, but reported effects on forage intake, lamb growth, milk production, reproductive responses or periparturient parasite status were context-dependent and are now of limited practical relevance where animal protein meals are restricted or cheaper protein sources are available (Hussein et al., 1991; Donaldson et al., 1998; Poppi et al., 1988).

Pigs 

Fish meal is mainly useful in pig nutrition as a high-quality, palatable and digestible protein source for weaned and nursery pigs. Its value is greatest when feed intake, gut adaptation and amino acid supply are limiting after weaning. It is much less commonly justified in grower-finisher pigs and sows, where its high price, variable availability and competition with other protein sources usually restrict its use. The quality of the fish meal is critical, as digestibility, energy value and amino acid availability can vary substantially between products (Cho et al., 2011; Kim et al., 2001; Yang et al., 2025).

In weaned and nursery pigs, fish meal has been used to improve growth performance, feed intake and feed efficiency during the post-weaning period. Its effects are linked to its high content of digestible protein, lysine, methionine, minerals and residual marine lipids, and to its generally good palatability. Older studies reported positive responses in starter and weaned pigs at inclusion rates below 10%, while higher inclusion rates were less attractive economically (Patience et al., 1995; Lopes et al., 2007; Zivkovic et al., 2007). More recent work also showed that fish meal source and inclusion level can affect nursery pig growth performance, confirming that fish meal remains a useful ingredient in high-value nursery diets when product quality and price are favourable (Jones et al., 2018).

Fish meal may also support digestive adaptation after weaning because it provides highly digestible amino acids and reduces the need for less digestible protein sources in early diets. It has sometimes been described as suitable for piglets with low health status or poor post-weaning performance, but its effects should not be interpreted as a systematic health response. Benefits depend on diet formulation, sanitary conditions, weaning age, inclusion level and the quality of the fish meal used (Bergstrom et al., 1997; Cho et al., 2011; Jones et al., 2018).

In grower-finisher pigs and sows, the practical interest of fish meal is more limited. These animals have lower requirements for very highly digestible protein sources than newly weaned pigs, and their diets can generally be balanced with vegetable protein sources, processed animal proteins where authorised, and crystalline amino acids. Fish meal may still have nutritional value, but it is rarely economically justified unless it is locally available, of good quality and competitively priced (Cho et al., 2011; Patience et al., 1995).

Fish meal has little specific interest for product quality in pig production. At normal inclusion levels in starter diets, it is not used to modify carcass or meat quality. However, poor-quality fish meal, oxidised lipids or excessive inclusion may reduce palatability and could theoretically contribute to undesirable odours or flavour problems, especially when used close to slaughter. From an environmental and nitrogen-use perspective, fish meal can be beneficial when its high digestibility and favourable amino acid profile allow more precise formulation of piglet diets, but this potential advantage is limited by cost, marine origin, competition with aquaculture and the availability of other highly digestible protein sources and crystalline amino acids (Cho et al., 2011; Patience et al., 1995; Yang et al., 2025).

The main practical constraints are cost, availability, variability between sources, lipid oxidation, biogenic amines and the risk of using low-quality or overheated products. Recent data obtained with different fish meal varieties in weaned pigs confirmed that nutrient digestibility and energy value can vary considerably between products, supporting the need for quality specifications and updated feed values rather than the use of a single generic fish meal value (Yang et al., 2025). In practice, fish meal is best regarded as a strategic ingredient for prestarter and starter diets rather than as a routine protein source for all pig categories.

Poultry 

Fish meal is a high-quality but expensive protein source for poultry. It is mainly useful in young birds, high-value diets, organic or low-synthetic-amino-acid formulations, and situations where palatability, digestible amino acids, minerals and marine lipids are valuable. Its routine use in commercial poultry feeds is limited by cost, variable quality, competition from other protein sources, lipid oxidation, biogenic amines and the possibility of fishy taints in meat or eggs. In poultry, quality control is particularly important because overheated or poorly processed fish meal may cause gizzard erosion through gizzerosine formation (Blair, 2008; Chadd, 2008; Cho et al., 2011; Sugahara, 1995; Jiao et al., 2024).

Broilers

In broilers, fish meal can improve performance when it supplies digestible protein, lysine, methionine, minerals and palatable nutrients in diets where these are limiting. Older sources reported improvements in body weight, daily gain and feed intake, but responses depend strongly on diet formulation, fish meal quality, age of the birds, inclusion level and the availability of cheaper protein sources (Blair, 2008; Reddy et al., 1989; Cho et al., 2011). Its value is greatest in starter, prestarter or nutritionally sensitive diets rather than as a routine protein source throughout the broiler cycle.

The health value of fish meal in broilers is mainly indirect. Good quality fish meal may support early feed intake and amino acid supply, but it should not be presented as a specific health-promoting ingredient. Conversely, poor-quality fish meal may impair health and performance. Excessive heating during drying can promote gizzerosine formation, and high levels of histamine or other biogenic amines may contribute to gizzard erosion, poor growth and mortality in poultry (Sugahara, 1995; Jiao et al., 2024).

Fish meal may improve the fatty acid profile of broiler meat when it provides long-chain n-3 fatty acids, but this is not its usual purpose in standard broiler production. High inclusion levels or poor-quality fish meal may cause fishy odours or off-flavours in meat, particularly when used close to slaughter or when residual lipids are oxidised (Hulan et al., 1988; Howe et al., 2002; Alagawany et al., 2019). Economically, fish meal should be regarded as a strategic ingredient for specific broiler diets; in conventional feeds, its high price and variability usually favour partial or total replacement by soybean meal, processed animal proteins, oilseed meals, crystalline amino acids or other high-quality protein sources (Blair, 2008; Chadd, 2008; Frempong et al., 2019).

Laying hens

In laying hens, fish meal can be used as a concentrated protein and mineral source, but its practical interest is more limited than in young broilers. When well processed and used at moderate levels, it can contribute digestible amino acids, phosphorus, calcium and trace elements, but modern layer diets are usually formulated with cheaper vegetable proteins, mineral supplements and crystalline amino acids (Blair, 2008; Chadd, 2008; Cho et al., 2011). Its main potential product-quality interest is the enrichment of eggs with long-chain n-3 fatty acids, particularly DHA, but marine lipids can also cause fishy odours or off-flavours, especially at high inclusion levels or when lipids are oxidised (Howe et al., 2002; Fraeye et al., 2012; Alagawany et al., 2019).

The health effects of fish meal in laying hens are mostly related to nutrient supply and feed quality. Poor-quality fish meal may increase the risk of biogenic amines, oxidative rancidity, microbial contamination or gizzerosine exposure, which is important because contaminants or off-flavours may be transferred to eggs (Sugahara, 1995; Jiao et al., 2024). Environmental benefits in layers should not be overstated: fish meal can be useful in precise formulation, but egg production systems generally have cheaper and more available ways to meet amino acid and mineral requirements.

Other poultry species

Fish meal has mainly a limited or specialised role in poultry species other than broilers and laying hens. Its use should be considered only where it improves diet quality, palatability or amino acid supply enough to justify its cost and quality-control requirements.

In young turkeys, fish meal has historically been valued because poults have high requirements for digestible amino acids and respond strongly to high-quality protein sources. Current use is constrained by cost, quality, availability and the availability of alternative proteins and synthetic amino acids (Potter et al., 1978; Blair, 2008; Chadd, 2008).

In quails and ducks, specific evidence on fish meal is limited and does not justify separate recommendations. Fish meal may be used as a dense animal protein and mineral source in local formulations, but its value depends on inclusion level, ingredient quality, diet balance and economic context. As in broilers and layers, excessive inclusion or poor-quality fish meal may increase the risk of off-flavours in meat or eggs, particularly when marine lipids are oxidised (Cho et al., 2011; Howe et al., 2002; Alagawany et al., 2019).

Rabbits 

Fish meal is a nutritionally valuable but marginal ingredient in rabbit feeding. It can provide high-quality protein, digestible amino acids, minerals and residual marine lipids, but its use is limited by cost, availability, variability and competition from cheaper protein sources. It should therefore be regarded as a specialised protein source rather than a routine ingredient, mainly where local fish by-products are available or where plant protein quality is limiting (Lebas, 2004; Gugołek et al., 2022).

In growing rabbits, fish meal has mostly been used in diets where local plant proteins were insufficient, poorly balanced or poorly digestible. Older studies showed that it could support growth at moderate inclusion levels, particularly in diets based on low-quality or fibrous local feedstuffs. In Cameroon, rabbits fed a fish meal-based protein diet had higher feed intake and daily gain than rabbits fed cassava leaf meal or cottonseed meal, but the fish meal diet was the least cost-effective (Fotso et al., 2000).

Fish meal may improve performance when it corrects amino acid deficiencies, particularly lysine and sulphur-containing amino acids, but responses depend on the whole diet rather than on fish meal alone. Studies using fish meal to adjust dietary energy and protein levels showed that rabbit performance and digestibility were strongly influenced by the balance between digestible energy and protein supply, including in reproductive does under tropical conditions (Prasad et al., 1996; Prasad et al., 1998).

There is no strong evidence that fish meal has a specific health-promoting effect in rabbits. Rabbit diets must remain primarily designed around fibre supply, digestive safety and prevention of enteric disorders. Excessive reliance on protein-rich ingredients may be undesirable if it increases undigested protein flow to the hindgut or reduces fibre balance. Fish meal quality is also important because oxidised lipids, biogenic amines, poor hygiene or excessive salt and ash may reduce feed intake or impair performance (Lebas, 2004; Gugołek et al., 2022).

Fish meal has little specific role in improving rabbit meat quality. From an environmental and economic perspective, its relevance depends mainly on whether it is produced from local fish processing by-products and whether its nutritional value compensates for its price and quality risks. In most rabbit production systems, fibrous plant feedstuffs and plant protein sources remain more practical and economical than fish meal (Lebas, 2004; Gugołek et al., 2022).

Horses and donkeys 

In horses, fish meal has occasionally been used as a high-quality protein supplement to improve the supply of digestible lysine and methionine, particularly in a series of studies on dietary protein and mare reproduction, where fish meal was used to modify the digestible amino acid supply. However, it is not a routine ingredient in modern equine feeding. In donkeys, no relevant feeding trials with fish meal were found, and their generally low protein requirements and reliance on fibrous feeds make fish meal unlikely to be of practical interest except in very specific deficiency situations (Van Niekerk et al., 1997; Martin-Rosset, 2018).

Fish 

Fish meal remains one of the reference protein sources in aquaculture, but its role has shifted from a routine bulk protein source to a more strategic ingredient. Its value depends strongly on fish species, feeding habit, trophic level, life stage and farming system. In carnivorous fish, such as salmonids and many marine species, it remains useful for its digestible protein, amino acid balance, palatability, minerals, marine lipids and functional compounds, particularly in juveniles, broodstock, stressful periods and demanding feeds. In omnivorous and herbivorous fish, such as tilapias, carps and many catfish, fish meal is less indispensable and can often be largely reduced or removed when diets are properly balanced for digestible amino acids, energy, minerals and palatability. Across species, the key question is not whether fish meal is nutritionally valuable, but how much is needed, at which life stage, and whether its use is supported by performance, health, product quality, environmental and economic outcomes (Tacon et al., 2008; FAO, 2025; Glencross et al., 2024b).

Salmonids

In salmonids, particularly Atlantic salmon and rainbow trout, fish meal has historically been a benchmark protein source because its amino acid profile, digestibility, palatability and mineral supply suit fast-growing carnivorous fish. It can support feed intake, growth, feed efficiency and nutrient retention, especially in juveniles and high-performance systems (Anderson et al., 1995; Sugiura et al., 1998; Tacon et al., 2008). However, modern salmonid feeds contain much less fish meal than earlier formulations, and high replacement levels are possible when diets combine plant proteins, processed animal proteins, single-cell proteins, insect meals, crystalline amino acids, suitable lipid sources and functional additives (Kaushik et al., 2008; FAO, 2025; Glencross et al., 2024b).

The health effects of reducing fish meal depend on the replacement strategy. Well-balanced low-fishmeal diets can maintain growth and feed conversion, whereas poorly formulated diets may reduce palatability, impair gut integrity, alter microbiota or increase sensitivity to stress and disease, particularly when high levels of some plant protein sources are used (Aragão et al., 2022; Dhar et al., 2024). Fish meal may therefore remain useful in diets for fry, smolts, stressful periods or formulations based on less attractive alternative ingredients.

For product quality, fish meal contributes high-quality protein and some marine nutrients, but salmonid flesh fatty acid profile is more strongly influenced by fish oil and other lipid sources. Replacing fish meal alone does not necessarily reduce flesh n-3 fatty acids, whereas replacing both fish meal and fish oil can lower EPA and DHA unless alternative marine or algal lipid sources are used. From an environmental and economic standpoint, reducing fish meal has lowered dependence on wild marine resources, but complete removal is not always the most efficient option if it impairs feed efficiency or requires costly alternative ingredients (Kaushik et al., 2008; Aragão et al., 2022; FAO, 2025; Glencross et al., 2024b).

Marine carnivorous fish

Marine carnivorous fish, such as European seabass, gilthead seabream, red seabream and yellowtail, have traditionally received diets with relatively high fish meal levels. Fish meal is valuable in these species because it improves feed intake, provides digestible amino acids and minerals, and supports growth in juveniles and demanding production stages (Nengas et al., 1995; Kaushik et al., 2004; Tacon et al., 2008). However, several marine carnivores can tolerate substantial fish meal replacement when alternative proteins are combined and diets are balanced for amino acids, phosphorus, energy and palatability (Kaushik et al., 2004; Kaushik et al., 2008; Glencross et al., 2024b).

In European seabass, almost total replacement of fish meal by plant protein sources was shown to be technically possible, but only with careful formulation rather than simple substitution by one plant ingredient (Kaushik et al., 2004). This remains the main lesson for marine carnivores: performance can be maintained with low-fishmeal diets only when the nutritional, sensory and functional roles of fish meal are compensated. Diets based heavily on alternative proteins may affect gut morphology, immune status, oxidative balance or nutrient digestibility if antinutritional factors, amino acid deficiencies or palatability limitations are not controlled (Aragão et al., 2022; Dhar et al., 2024).

Fish meal is not the only determinant of fillet quality. Low-fishmeal diets may modify fillet composition, mineral deposition or sensory traits depending on the alternative ingredients used, while the n-3 fatty acid profile depends mainly on dietary lipid sources. Economically, fish meal may remain useful in high-value juveniles, broodstock or premium diets, but feeds for the grow-out phase increasingly rely on combinations of alternative ingredients and targeted fish meal inclusion (Kaushik et al., 2008; Glencross et al., 2024b).

Omnivorous and herbivorous fish

Tilapias

Tilapias are omnivorous fish and are much less dependent on fish meal than salmonids or marine carnivores. In intensive feeds, fish meal can improve palatability, protein quality and early growth, particularly in fry and fingerlings, but feeds for the grow-out phase can often contain little or no fish meal when plant proteins, animal by-products or other local protein sources are properly balanced (Tacon et al., 2008; Glencross et al., 2024b). In semi-intensive systems, natural pond productivity further reduces dependence on fish meal.

Performance responses depend mainly on the quality of replacement ingredients. Soybean meal, oilseed meals, cereal by-products, animal protein meals, insect meals, microbial proteins and local by-products can replace much or all of the fish meal when diets meet digestible amino acid and energy requirements and antinutritional factors are controlled (Aragão et al., 2022; Glencross et al., 2024b). Poorly balanced replacements may reduce growth, feed intake or feed conversion, but this reflects formulation failure rather than a strict requirement for high fish meal inclusion.

Health effects are also formulation-dependent. Moderate replacement by good-quality alternative proteins can maintain gut function and immune status, whereas excessive use of poorly processed plant ingredients may alter intestinal structure, microbiota and inflammatory responses (Aragão et al., 2022; Dhar et al., 2024). Fish meal may remain useful in early diets or when palatability and amino acid balance are limiting, but it is not normally required as a major protein source in feeds for the grow-out phase. Economically and environmentally, low-fishmeal or fishmeal-free diets are particularly relevant where affordable local plant and agricultural by-products are available (FAO, 2025; Glencross et al., 2024b).

Carps

Carps and other cyprinids are omnivorous to herbivorous fish and are among the aquaculture species least dependent on fish meal. In many semi-intensive pond systems, carps receive feeds with little or no fish meal, and their nutrition is supported by natural food, cereals, oilseed meals, brans and other plant-based ingredients (Tacon et al., 2008; Médale et al., 2009). Fish meal may improve protein quality and growth in some intensive diets, but it is rarely indispensable.

The performance value of fish meal in carp diets depends on species, life stage and culture intensity. Common carp can digest fish meal protein well, but it can also use plant proteins efficiently when diets are balanced and water temperature, digestibility and amino acid supply are considered (Kim et al., 1998). In rohu and other Indian major carps, fish meal replacement by improved plant protein sources may be possible when limiting amino acids are supplemented and ingredient quality is controlled (Mukhopadhyay, 2000).

Health and product-quality effects of fish meal in carp are not strong enough to support routine high inclusion. As with tilapia, poor-quality replacement diets may impair growth or gut condition, but well-formulated plant and local ingredients can support satisfactory performance. From an environmental and economic perspective, reducing fish meal is usually relevant because carps can use lower-trophic feed resources, natural pond productivity and locally available plant feedstuffs efficiently (Médale et al., 2009; FAO, 2025).

Catfish

Catfish include channel catfish, African catfish, pangasius and other farmed siluriforms. They are generally omnivorous or opportunistic carnivores and can use a wide range of protein sources. Fish meal can improve palatability and amino acid quality, especially in juvenile diets, but many catfish systems use low-fishmeal diets or replace fish meal with soybean meal, oilseed meals, animal by-products, blood meal, insect meals or local feed resources (Tacon et al., 2008; Glencross et al., 2024b).

Performance responses depend on species and replacement ingredient. African catfish and pangasius can often perform well with low-fishmeal diets when protein quality, energy balance and feed intake are maintained. Channel catfish diets have long relied heavily on plant protein sources, especially soybean meal, and fish meal is usually useful only when it improves performance, palatability or early growth enough to compensate for its cost. The main nutritional risks of replacement are amino acid imbalance, poor digestibility, antinutritional factors and low palatability rather than the absence of fish meal itself (Aragão et al., 2022; Dhar et al., 2024).

Fish meal has no systematic product-quality advantage in catfish. Flesh quality depends more on growth rate, lipid source, water quality, finishing diet and processing conditions. Economically, fish meal is often difficult to justify in feeds for the grow-out phase because production is usually cost-sensitive. Environmentally, the use of low-trophic and locally available feed ingredients is generally consistent with catfish feeding biology and production economics (FAO, 2025; Glencross et al., 2024b).

Crustaceans 

Fish meal remains a valuable ingredient in crustacean feeds, especially for penaeid shrimps, because it provides digestible protein, essential amino acids, minerals, marine lipids, attractants and feeding stimulants. Its practical value is greatest in marine shrimp feeds, early life stages, nursery diets and intensive systems where feed intake, growth and survival depend strongly on diet quality. However, fish meal should now be considered as a high-value functional protein source rather than as a bulk ingredient. Its inclusion level depends on species, life stage, farming system, natural food availability, ingredient prices and the capacity of alternative proteins, attractants and functional ingredients to maintain performance, health and feed efficiency (Tacon et al., 2008; Amaya et al., 2008; FAO, 2025; Chen et al., 2024).

Marine shrimps

Marine shrimps, particularly Pacific white shrimp (Litopenaeus vannamei) and black tiger shrimp (Penaeus monodon), have historically received relatively high levels of fish meal. Older practical diets sometimes contained up to about 40% fish meal, but current formulations increasingly use lower inclusion rates and a wider range of alternative protein sources (Amaya et al., 2008; Tacon et al., 2008; Chen et al., 2024).

Fish meal supports shrimp performance through its amino acid balance, digestibility, palatability, mineral supply and feeding stimulation. It is particularly useful in post-larval and juvenile stages, high-density systems and low-natural-food conditions. However, substantial replacement is possible in L. vannamei when diets are properly balanced for digestible amino acids, energy, minerals and palatability, and when attractants or functional ingredients compensate for the loss of fish meal-derived feeding stimuli (Chen et al., 2024; Glencross et al., 2024b).

Replacement of fish meal in shrimp diets is not a simple protein substitution. It may affect feed attraction, feeding behaviour, gut function, hepatopancreas condition, antioxidant status and immune responses. Well-formulated low-fishmeal diets can maintain growth, survival and feed conversion, but poorly balanced replacements may reduce feed intake, digestibility, disease resistance or oxidative status (Dhar et al., 2024; Chen et al., 2024; Kasamechotchung et al., 2025).

Fish meal has no unique effect on shrimp product quality beyond supporting growth and nutrient deposition. Shrimp composition and sensory quality depend on the whole diet, culture system, water quality and lipid sources. From an environmental and economic point of view, reducing fish meal may lower dependence on wild marine resources and reduce feed cost, but only if survival, growth and feed efficiency are maintained. Fish meal is therefore most useful in shrimp feeds when it is targeted to stages or systems where its palatability, digestibility and functional effects are difficult to replace (FAO, 2025; Glencross et al., 2024b; Chen et al., 2024).

Freshwater prawns

Freshwater prawns, particularly Macrobrachium rosenbergii, are generally less dependent on fish meal than marine shrimps. Fish meal may be useful in post-larval and juvenile feeds because it improves palatability and amino acid supply, but high inclusion is rarely justified in feeds for the grow-out phase. Plant proteins, animal by-products and local feed resources can often replace much of the fish meal when diets remain balanced for amino acids, energy, digestibility and feed acceptance (Dhar et al., 2024; Glencross et al., 2024b).

Product-quality effects are usually secondary in freshwater prawns. Economically, reducing fish meal is often relevant because freshwater prawn farming is frequently cost-sensitive and may rely on local feed resources. Fish meal is therefore best reserved for nursery diets, specialised feeds or situations where local ingredients are nutritionally limiting (Dhar et al., 2024; Glencross et al., 2024b).

Crabs and other crustaceans

Crab nutrition is less standardised than shrimp nutrition, and formulated feeds for mud crabs, swimming crabs and Chinese mitten crabs are still developing. Fish meal may support growth, moulting, survival and reproduction by supplying digestible protein, amino acids, minerals and marine nutrients, but feed acceptance, attractants, lipid nutrition and species-specific requirements are also critical (Esmaeili et al., 2024).

For crabs, crayfish, lobsters and other crustaceans, the value of fish meal depends on species, life stage, feeding behaviour, natural food availability and market value. In lower-intensity systems, natural productivity and local feedstuffs may reduce the need for high fish meal inclusion. In high-value juvenile or nursery feeds, fish meal may remain useful where palatability, feed acceptance and digestible protein are critical (Esmaeili et al., 2024; FAO, 2025).

Nutritional tables

Avg: average or predicted value; SD: standard deviation; Min: minimum value; Max: maximum value; Nb: number of values (samples) used

Main analysis Unit Avg SD Min Max Nb  
Dry matter % as fed 92.2 1.4 83.1 97.8 795  
Crude protein % DM 74.8 3.8 57.4 81 82  
Crude fibre % DM 0          
Neutral detergent fibre % DM 5.8 2.6 3.1 9 5  
Acid detergent fibre % DM 0.3 0.3 0 0.6 6  
Lignin % DM 0.2 0.2 0 0.3 6  
Ether extract % DM 9.8 1.8 2.5 15.3 425 *
Ash % DM 15.2 3.3 6 33.8 715  
Insoluble ash % DM 0.5 0.8 0.03 4.9 37  
Starch (polarimetry) % DM 0   0 0 2  
Starch (enzymatic) % DM 0          
Total sugars % DM 0          
Gross energy MJ/kg DM 21.3 1.3 18.3 23.3 17 *
               
Amino acids Unit Avg SD Min Max Nb  
Alanine g/16g N 6.2 0.3 5.3 7.3 126 *
Arginine g/16g N 6.5 1.3 3.2 9.5 127 *
Aspartic acid g/16g N 9.1 0.8 6.9 11.4 129 *
Cystine g/16g N 0.8 0.1 0.5 1.4 109 *
Glutamic acid g/16g N 12.7 0.9 10.1 15 129 *
Glycine g/16g N 6.2 0.8 4.2 11.1 129 *
Histidine g/16g N 2.4 0.7 1.5 4.2 83 *
Isoleucine g/16g N 4.2 0.4 2.3 5.3 133 *
Leucine g/16g N 7.2 0.5 5.1 8.2 131 *
Lysine g/16g N 7.5 0.6 5.7 9.4 156 *
Methionine g/16g N 2.8 0.3 1.6 3.7 125 *
Methionine+cystine g/16g N 3.6 0.3 2.1 4.6 108 *
Phenylalanine g/16g N 3.9 0.3 3.2 4.7 132 *
Phenylalanine+tyrosine g/16g N 7 0.5 5.6 8.2 89 *
Proline g/16g N 4 0.5 3.5 6.5 73  
Serine g/16g N 3.9 0.4 2.1 4.9 130 *
Threonine g/16g N 4.1 0.3 3.5 5.3 132 *
Tryptophan g/16g N 1 0.1 0.6 1.4 69 *
Tyrosine g/16g N 3.1 0.4 1.7 4.1 92 *
Valine g/16g N 5 0.4 4 6.3 129 *
               
Fatty acids Unit Avg SD Min Max Nb  
Myristic acid C14:0 % fatty acids 6 2.3 2.8 11.2 15  
Palmitic acid C16:0 % fatty acids 17.8 4.7 10.3 28.2 15  
Palmitoleic acid C16:1 % fatty acids 7.2 2.3 4.2 12.3 15  
Stearic acid C18:0 % fatty acids 3.6 1.6 0.6 6.4 15  
Oleic acid C18:1 % fatty acids 12.3 3.9 5.5 20.2 15  
Linoleic acid C18:2 % fatty acids 2.1 1.3 0.7 4.5 6  
Linolenic acid C18:3 % fatty acids 1.9   1.5 2.2 2  
               
Minerals Unit Avg SD Min Max Nb  
Calcium g/kg DM 33.7 12.2 0.9 81.9 446 *
Phosphorus g/kg DM 24.8 4.3 14.5 50.9 440 *
Potassium g/kg DM 9.5 2.2 4.7 14.5 48 *
Sodium g/kg DM 9.97 2.98 2.83 21.41 172  
Chlorine g/kg DM 15.5 6 2.1 37.4 294  
Magnesium g/kg DM 2.3 0.7 1.4 3.5 12 *
Sulfur g/kg DM 7.3          
Manganese mg/kg DM 13 14 2 41 9  
Zinc mg/kg DM 103 21 75 147 14  
Copper mg/kg DM 10 2 5 12 10  
Iron mg/kg DM 314 187 90 758 21 *
Selenium mg/kg DM 0.4          
               
Pig nutritive values Unit Avg SD Min Max Nb  
Energy digestibility, growing pig % 85          
DE growing pig MJ/kg DM 18.1         *
MEn growing pig MJ/kg DM 16.3         *
NE growing pig MJ/kg DM 10.5         *
Nitrogen digestibility, growing pig % 85          
               
Poultry nutritive values Unit Avg SD Min Max Nb  
AMEn cockerel MJ/kg DM 15.3         *
AMEn broiler MJ/kg DM 15.3         *
               
Ruminants nutritive values Unit Avg SD Min Max Nb  
OM digestibility, ruminants % 95.3   93 97.7 3  
Energy digestibility, ruminants % 97.1         *
ME ruminants MJ/kg DM 14.3         *
Nitrogen degradability (effective, k=6%) % 51 8 31 57 8 *
Nitrogen degradability (effective, k=4%) % 55         *
a (N) % 30 8 17 48 16  
b (N) % 41 24 15 120 16  
c (N) h-1 0.061 0.062 0.006 0.21 16  
               
Rabbit nutritive values Unit Avg SD Min Max Nb  
DE rabbit MJ/kg DM 20.7         *
MEn rabbit MJ/kg DM 18.4         *
Energy digestibility, rabbit % 97.3         *
Nitrogen digestibility, rabbit % 59.4         *

The asterisk * indicates that the average value was obtained by an equation.

References

Abdou Dade et al., 1990; Adamidou et al., 2009; AFZ, 2025; Alegbeleye et al., 2012; Allan et al., 2000; Anon., 2001; Aufrère et al., 1991; Aureli et al., 2015; Balogun, 2011; Barlow et al., 1979; Barrows et al., 2015; Bochi-Brum et al., 1999; Borgeson et al., 2006; Bryan et al., 2019; Charalambous et al., 1999; Chiou et al., 1995; CIRAD, 1991; CIRAD, 2008; De Boever et al., 1984; De Silva et al., 1990; Dewar, 1967; Djouvinov et al., 1998; El-Haroun et al., 2007; Garg et al., 2002; González et al., 1998; Guimaraes et al., 2008; IAFMM, 1985; Jentsch et al., 1992; Jongbloed et al., 1990; Khandaker et al., 1996; Knaus et al., 1998; Landry et al., 1988; Lechevestrier, 1996; Lindberg, 1981; Lodhi et al., 1976; Mantysaari et al., 1989; Masoero et al., 1994; Mlay et al., 2006; Morgan et al., 1984; Moyano et al., 1992; Nguyen Nhut Xuan Dung et al., 2002; Oluyemi et al., 1976; Opstvedt, 1984; Pozy et al., 1996; Rangacharyulu et al., 2003; Schang et al., 1982; Susmel et al., 1989; Urbaityte et al., 2009; Wang Dun et al., 2005; Wohlt et al., 1991

Last updated on 07/07/2026 15:29:01

Main analysis Unit Avg SD Min Max Nb  
Dry matter % as fed 92.1 1.8 83.1 98.9 1811  
Crude protein % DM 70.7 3.3 57.4 76.3 103  
Crude fibre % DM 0 0.5 0 2.1 31  
Neutral detergent fibre % DM 5.8 2.6 3.1 9 5  
Acid detergent fibre % DM 0.5 0.5 0 1.6 7  
Lignin % DM 0.2 0.2 0 0.3 6  
Ether extract % DM 10 1.6 2.1 16.6 1000 *
Ash % DM 18.2 3 7.3 33.8 1702  
Insoluble ash % DM 0.5 1.1 0.02 5.7 116  
Starch (polarimetry) % DM 0       1  
Starch (enzymatic) % DM 0          
Total sugars % DM 0       1  
Gross energy MJ/kg DM 20.5 0.9 19.5 22.9 26 *
               
Amino acids Unit Avg SD Min Max Nb  
Alanine g/16g N 6.3 0.4 4.2 7.8 129 *
Arginine g/16g N 6.2 0.9 3.2 9.1 128 *
Aspartic acid g/16g N 9.1 1 6.4 11.5 129 *
Cystine g/16g N 0.9 0.1 0.5 1.4 85 *
Glutamic acid g/16g N 12.6 1 8.6 15.8 129 *
Glycine g/16g N 6.7 1.1 4 12.9 128 *
Histidine g/16g N 2.5 0.7 0.9 4.3 82 *
Isoleucine g/16g N 4.1 0.5 2.3 5.3 137 *
Leucine g/16g N 7.2 0.5 5 8.6 134 *
Lysine g/16g N 7.5 0.8 4.2 9.7 149 *
Methionine g/16g N 2.7 0.4 1.3 3.4 116 *
Methionine+cystine g/16g N 3.6 0.4 2.1 4.5 86 *
Phenylalanine g/16g N 3.9 0.3 2.7 4.7 134 *
Phenylalanine+tyrosine g/16g N 6.9 0.5 5.6 8.2 111 *
Proline g/16g N 4.3 0.8 3 8 59  
Serine g/16g N 3.9 0.5 2.1 6.8 129 *
Threonine g/16g N 4.1 0.4 2.7 5.3 135 *
Tryptophan g/16g N 1 0.2 0.6 1.3 47 *
Tyrosine g/16g N 3 0.4 1.7 3.7 112 *
Valine g/16g N 5 0.4 3.3 6.3 133 *
               
Fatty acids Unit Avg SD Min Max Nb  
Myristic acid C14:0 % fatty acids 6 2.3 2.8 11.2 15  
Palmitic acid C16:0 % fatty acids 17.8 4.7 10.3 28.2 15  
Palmitoleic acid C16:1 % fatty acids 7.2 2.3 4.2 12.3 15  
Stearic acid C18:0 % fatty acids 3.6 1.6 0.6 6.4 15  
Oleic acid C18:1 % fatty acids 12.3 3.9 5.5 20.2 15  
Linoleic acid C18:2 % fatty acids 2.1 1.3 0.7 4.5 6  
Linolenic acid C18:3 % fatty acids 1.9   1.5 2.2 2  
               
Minerals Unit Avg SD Min Max Nb  
Calcium g/kg DM 44.8 11.7 12.9 83.8 1034 *
Phosphorus g/kg DM 28.6 4.2 16.3 46.3 1027 *
Potassium g/kg DM 8.5 2.2 4.7 14.5 76 *
Sodium g/kg DM 11.47 3.16 3.77 20.91 335  
Chlorine g/kg DM 17.8 6.6 1.5 37.4 660  
Magnesium g/kg DM 2.4 0.6 0.8 4.3 27 *
Sulfur g/kg DM 7.8          
Manganese mg/kg DM 19 10 3 41 24  
Zinc mg/kg DM 107 19 74 147 24  
Copper mg/kg DM 12 23 3 115 22  
Iron mg/kg DM 382 171 90 758 43 *
Selenium mg/kg DM 0.4   0.4 0.5 3  
               
Pig nutritive values Unit Avg SD Min Max Nb  
Energy digestibility, growing pig % 85          
DE growing pig MJ/kg DM 17.4         *
MEn growing pig MJ/kg DM 15.7         *
NE growing pig MJ/kg DM 10.2         *
Nitrogen digestibility, growing pig % 85          
               
Poultry nutritive values Unit Avg SD Min Max Nb  
AMEn cockerel MJ/kg DM 14.5         *
AMEn broiler MJ/kg DM 14.5         *
               
Ruminants nutritive values Unit Avg SD Min Max Nb  
Energy digestibility, ruminants % 95.9         *
ME ruminants MJ/kg DM 13.6         *
Nitrogen digestibility, ruminants % 81         *
Nitrogen degradability (effective, k=6%) % 51 8 31 54 10 *
Nitrogen degradability (effective, k=4%) % 55         *
a (N) % 30 8 17 48 16  
b (N) % 41 24 15 120 16  
c (N) h-1 0.061 0.062 0.006 0.21 16  
               
Rabbit nutritive values Unit Avg SD Min Max Nb  
DE rabbit MJ/kg DM 19.3         *
MEn rabbit MJ/kg DM 16.7         *
Energy digestibility, rabbit % 94.5         *
Nitrogen digestibility, rabbit % 74.8         *

The asterisk * indicates that the average value was obtained by an equation.

References

Adamidou et al., 2009; ADAS, 1988; Adewolu et al., 2010; AFZ, 2025; Alegbeleye et al., 2012; Allan et al., 2000; Al-Marzooqi et al., 2015; Anderson et al., 1991; Anon., 2001; Aufrère et al., 1991; Aureli et al., 2015; Balogun, 2011; Barlow et al., 1979; Barrows et al., 2015; Bochi-Brum et al., 1999; Borgeson et al., 2006; Bryden et al., 2009; Burgoon et al., 1992; Chiou et al., 1995; CIRAD, 1991; CIRAD, 1994; CIRAD, 2008; De Silva et al., 1990; Dewar, 1967; Djouvinov et al., 1998; El-Haroun et al., 2007; Fanimo et al., 2004; Garcia et al., 2007; Garg et al., 2002; González et al., 1998; Guimaraes et al., 2008; Holm, 1971; IAFMM, 1985; Iyayi et al., 2014; Jentsch et al., 1992; Jongbloed et al., 1990; Khandaker et al., 1996; Knaus et al., 1998; Landry et al., 1988; Lechevestrier, 1996; Lindberg, 1981; Lodhi et al., 1976; Mantysaari et al., 1989; Mariscal Landin, 1992; Masoero et al., 1994; Mlay et al., 2006; Morgan et al., 1984; Moyano et al., 1992; Nguyen Nhut Xuan Dung et al., 2002; Oluyemi et al., 1976; Opstvedt, 1984; Owusu-Domfeh et al., 1970; Petit, 1992; Pozy et al., 1996; Rangacharyulu et al., 2003; Richter et al., 2003; Sanz et al., 1994; Smith et al., 1986; Sogbesan et al., 2006; Sogbesan et al., 2008; Susmel et al., 1989; Susmel et al., 1989; Wang Dun et al., 2005; Wohlt et al., 1991; Yamazaki et al., 1986; Yoo et al., 2019

Last updated on 07/07/2026 15:30:46

Main analysis Unit Avg SD Min Max Nb  
Dry matter % as fed 92.3 2.1 78.2 98.9 1297  
Crude protein % DM 67.8 3.2 57.4 76.3 97  
Crude fibre % DM 0 0.7 0 2.6 30  
Neutral detergent fibre % DM 5.8 2.6 3.1 9 5  
Acid detergent fibre % DM 0.7 0.7 0 1.8 8  
Lignin % DM 0.2 0.2 0 0.3 6  
Ether extract % DM 10.3 1.9 2.1 18 702 *
Ash % DM 19.3 3.3 7.3 33.8 1233  
Insoluble ash % DM 0.6 1.3 0.02 5.7 99  
Starch (polarimetry) % DM 0          
Starch (enzymatic) % DM 0          
Total sugars % DM 0       1  
Gross energy MJ/kg DM 20.2 0.9 19.5 22.9 24 *
               
Amino acids Unit Avg SD Min Max Nb  
Alanine g/16g N 6.4 0.5 4.2 7.8 84 *
Arginine g/16g N 6 0.8 3.2 8.2 87 *
Aspartic acid g/16g N 9.1 1 6.4 11.5 85 *
Cystine g/16g N 0.9 0.2 0.5 1.4 55 *
Glutamic acid g/16g N 12.5 1.1 8.6 15.8 85 *
Glycine g/16g N 7 1.3 4 12.9 84 *
Histidine g/16g N 2.6 0.7 0.9 4.2 61 *
Isoleucine g/16g N 4.1 0.6 1.8 5 93 *
Leucine g/16g N 7.2 0.6 5 8.6 89 *
Lysine g/16g N 7.5 0.9 4.2 9.7 100 *
Methionine g/16g N 2.7 0.4 1.3 3.4 84 *
Methionine+cystine g/16g N 3.5 0.4 2.1 4.5 56 *
Phenylalanine g/16g N 3.9 0.3 2.7 4.7 89 *
Phenylalanine+tyrosine g/16g N 6.9 0.6 5.6 8.2 74 *
Proline g/16g N 4.6 0.9 3 8 42  
Serine g/16g N 3.9 0.7 2.1 6.8 84 *
Threonine g/16g N 4.1 0.4 2.7 5.3 91 *
Tryptophan g/16g N 1 0.2 0.6 1.3 25 *
Tyrosine g/16g N 3 0.4 1.7 3.7 75 *
Valine g/16g N 5 0.5 3.3 6.5 89 *
               
Fatty acids Unit Avg SD Min Max Nb  
Myristic acid C14:0 % fatty acids 6 2.3 2.8 11.2 15  
Palmitic acid C16:0 % fatty acids 17.8 4.7 10.3 28.2 15  
Palmitoleic acid C16:1 % fatty acids 7.2 2.3 4.2 12.3 15  
Stearic acid C18:0 % fatty acids 3.6 1.6 0.6 6.4 15  
Oleic acid C18:1 % fatty acids 12.3 3.9 5.5 20.2 15  
Linoleic acid C18:2 % fatty acids 2.1 1.3 0.7 4.5 6  
Linolenic acid C18:3 % fatty acids 1.9   1.5 2.2 2  
               
Minerals Unit Avg SD Min Max Nb  
Calcium g/kg DM 48.6 13.3 17.4 93.9 667 *
Phosphorus g/kg DM 29.9 5.3 16.3 55.6 660 *
Potassium g/kg DM 8.2 2.9 0.5 14.5 36 *
Sodium g/kg DM 11.76 3.4 2.69 21.09 245  
Chlorine g/kg DM 18.4 6.7 1.5 35.5 452  
Magnesium g/kg DM 2.4 0.6 0.8 4.3 27 *
Sulfur g/kg DM 7.8          
Manganese mg/kg DM 20 10 3 41 24  
Zinc mg/kg DM 107 17 74 132 23  
Copper mg/kg DM 12 23 3 115 22  
Iron mg/kg DM 405 176 115 758 31 *
Selenium mg/kg DM 0.4   0.4 0.5 2  
               
Pig nutritive values Unit Avg SD Min Max Nb  
Energy digestibility, growing pig % 85          
DE growing pig MJ/kg DM 17.1         *
MEn growing pig MJ/kg DM 15.5         *
NE growing pig MJ/kg DM 10.1         *
Nitrogen digestibility, growing pig % 85          
               
Poultry nutritive values Unit Avg SD Min Max Nb  
AMEn cockerel MJ/kg DM 14.1         *
AMEn broiler MJ/kg DM 14.1         *
               
Ruminants nutritive values Unit Avg SD Min Max Nb  
OM digestibility, ruminants % 95.3   93 97.7 3  
Energy digestibility, ruminants % 95.4         *
ME ruminants MJ/kg DM 13.5         *
Nitrogen degradability (effective, k=6%) % 51 8 31 55 10 *
Nitrogen degradability (effective, k=4%) % 55         *
a (N) % 30 8 17 48 16  
b (N) % 41 24 15 120 16  
c (N) h-1 0.061 0.062 0.006 0.21 16  
               
Rabbit nutritive values Unit Avg SD Min Max Nb  
DE rabbit MJ/kg DM 18.7         *
MEn rabbit MJ/kg DM 15.9         *
Energy digestibility, rabbit % 92.6         *
Nitrogen digestibility, rabbit % 82.7         *

The asterisk * indicates that the average value was obtained by an equation.

References

Adamidou et al., 2009; ADAS, 1988; Adewolu et al., 2010; AFZ, 2025; Agunbiade et al., 2004; Akinleye et al., 2012; Alegbeleye et al., 2012; Allan et al., 2000; Al-Marzooqi et al., 2015; Anderson et al., 1991; Anon., 2001; Aufrère et al., 1991; Awoniyi et al., 2003; Balogun, 2011; Barlow et al., 1979; Barrows et al., 2015; Bochi-Brum et al., 1999; Bryden et al., 2009; Burgoon et al., 1992; CIRAD, 1991; CIRAD, 1994; CIRAD, 2008; De Silva et al., 1990; Dewar, 1967; Fanimo et al., 2004; Garcia et al., 2007; Garg et al., 2002; González et al., 1998; Guimaraes et al., 2008; Han et al., 1976; Holm, 1971; IAFMM, 1985; Iyayi et al., 2014; Jentsch et al., 1992; Jongbloed et al., 1990; Kamalak et al., 2005; Khandaker et al., 1996; Knaus et al., 1998; Landry et al., 1988; Lechevestrier, 1992; Lechevestrier, 1996; Lindberg, 1981; Lodhi et al., 1976; Longe et al., 1988; Mantysaari et al., 1989; Mariscal Landin, 1992; Masoero et al., 1994; Mlay et al., 2006; Moyano et al., 1992; Nguyen Nhut Xuan Dung et al., 2002; Oluyemi et al., 1976; Opstvedt, 1984; Owusu-Domfeh et al., 1970; Petit, 1992; Pozy et al., 1996; Richter et al., 2003; Sanz et al., 1994; Smith et al., 1986; Sogbesan et al., 2006; Sogbesan et al., 2008; Susmel et al., 1989; Susmel et al., 1989; Vervaeke et al., 1989; Wang Dun et al., 2005; Wohlt et al., 1991; Yamazaki et al., 1986; Yin et al., 1993; Yoo et al., 2019

Last updated on 07/07/2026 15:47:36

Main analysis Unit Avg SD Min Max Nb  
Dry matter % as fed 90.8 3.2 78.9 96.5 75  
Crude protein % DM 49.4 3 44 55.8 67  
Crude fibre % DM 2 1.7 0.1 6.5 27  
Neutral detergent fibre % DM 17.3 13.5 4.5 39.3 5  
Acid detergent fibre % DM 1.2   0.4 2.3 4  
Lignin % DM 0.5   0.06 1.1 3  
Ether extract % DM 12.3 4.6 2.8 20 23 *
Ash % DM 30.7 8.5 6.4 45.8 76  
Insoluble ash % DM 8.4 8.5 0.2 26.3 18  
Starch (polarimetry) % DM 0.7          
Total sugars % DM 0.3          
Gross energy MJ/kg DM 17.3   15.9 19.1 3 *
               
Amino acids Unit Avg SD Min Max Nb  
Alanine g/16g N 7         *
Arginine g/16g N 3.8   3.5 6.1 3 *
Aspartic acid g/16g N 9.2   6.3 11 3 *
Cystine g/16g N 1         *
Glutamic acid g/16g N 11.6   9.8 14.5 2 *
Glycine g/16g N 9.8         *
Histidine g/16g N 3.4         *
Isoleucine g/16g N 3.6   3.2 3.9 3 *
Leucine g/16g N 7.1   5.4 8.2 3 *
Lysine g/16g N 7.2   4.4 7.9 3 *
Methionine g/16g N 2.2   1.7 2.9 3 *
Methionine+cystine g/16g N 3.2   2.3 3.8 3 *
Phenylalanine g/16g N 4   3.1 4.5 3 *
Phenylalanine+tyrosine g/16g N 6.7         *
Proline g/16g N 6       1  
Serine g/16g N 3.8   2.6 4.7 2 *
Threonine g/16g N 4.1   2.7 4.6 3 *
Tryptophan g/16g N 0.7         *
Tyrosine g/16g N 2.7         *
Valine g/16g N 5   4 5.9 3 *
               
Fatty acids Unit Avg SD Min Max Nb  
Myristic acid C14:0 % fatty acids 6 2.3 2.8 11.2 15  
Palmitic acid C16:0 % fatty acids 17.8 4.7 10.3 28.2 15  
Palmitoleic acid C16:1 % fatty acids 7.2 2.3 4.2 12.3 15  
Stearic acid C18:0 % fatty acids 3.6 1.6 0.6 6.4 15  
Oleic acid C18:1 % fatty acids 12.3 3.9 5.5 20.2 15  
Linoleic acid C18:2 % fatty acids 2.1 1.3 0.7 4.5 6  
Linolenic acid C18:3 % fatty acids 1.9   1.5 2.2 2  
               
Minerals Unit Avg SD Min Max Nb  
Calcium g/kg DM 90.2 24.9 21.4 113 30 *
Phosphorus g/kg DM 44.3 11 19.2 56.2 28 *
Potassium g/kg DM 4.8   4.7 9.6 2 *
Sodium g/kg DM 9.47 3.39 3.46 13.42 11  
Chlorine g/kg DM 16.7 7.9 4.9 38.6 22  
Magnesium g/kg DM 2.8         *
Manganese mg/kg DM 20   7 36 3  
Zinc mg/kg DM 136          
Copper mg/kg DM 12   6 12 3  
Iron mg/kg DM 660   566 758 3 *
               
Poultry nutritive values Unit Avg SD Min Max Nb  
AMEn cockerel MJ/kg DM 11.1         *
AMEn broiler MJ/kg DM 11.1         *
               
Ruminants nutritive values Unit Avg SD Min Max Nb  
OM digestibility, ruminants % 95.3   93 97.7 3  
Energy digestibility, ruminants % 91.3         *
ME ruminants MJ/kg DM 11.4         *
Nitrogen digestibility, ruminants % 80.6         *
Nitrogen degradability (effective, k=6%) % 51   42 57 3 *
Nitrogen degradability (effective, k=4%) % 55         *
a (N) % 30 8 17 48 16  
b (N) % 41 24 15 120 16  
c (N) h-1 0.061 0.062 0.006 0.21 16  
Dry matter degradability (effective, k=6%) % 47       1 *
Dry matter degradability (effective, k=4%) % 50       1 *
a (DM) % 23   8 29 4  
b (DM) % 36   21 57 4  
c (DM) h-1 0.126   0.05 0.21 4  
               
Rabbit nutritive values Unit Avg SD Min Max Nb  
DE rabbit MJ/kg DM 13.9         *
MEn rabbit MJ/kg DM 11.4         *
Energy digestibility, rabbit % 79.9         *
Nitrogen digestibility, rabbit % 100         *

The asterisk * indicates that the average value was obtained by an equation.

References

AFZ, 2025; Balogun, 2011; Bindu et al., 2004; CIRAD, 2008; Dewar, 1967; Donkoh et al., 2009; Fagoonee, 1983; Garg et al., 2002; Habib et al., 2013; Hira et al., 2002; Horvli et al., 1994; Hossain et al., 1997; Huque et al., 1996; Islam et al., 1997; Jongbloed et al., 1990; Khandaker et al., 1996; Knaus et al., 1998; Laining et al., 2004; Lebas et al., 2012; Lodhi et al., 1976; Marghazani et al., 2013; Mondal et al., 2008; Nguyen Nhut Xuan Dung et al., 2003; Opstvedt, 1984; Pozy et al., 1996; Reddy, 1997; Ullah et al., 2016

Last updated on 07/07/2026 15:43:28

References
References 
Datasheet citation 

Heuzé V., Tran G., Kaushik S., 2026. Fish meal. Feedipedia, a programme by INRAE, CIRAD, AFZ and FAO. https://www.feedipedia.org/node/208 Last updated on July 13, 2026, 13:36

English correction by Tim Smith (Animal Science consultant) and Hélène Thiollet (AFZ)