Feedipedia
Animal feed resources information system
Feedipedia
Feedipedia

Did you find the information you were looking for? Is it valuable to you? Feedipedia is encountering funding shortage. We need your help to keep providing reference-based feeding recommendations for your animals.
Would you consider donating? If yes, please click on the button Donate.

Any amount is the welcome. Even one cent is helpful to us!

Soybean meal

Datasheet

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

Soybean meal, soyabean meal, soya bean meal, soybean cake, soybean oil meal, soybean oil cake [English]; 大豆粕 [Chinese]; सोयबीन आहार [Hindi]; Torta de soja [Spanish]; مسحوق فول الصويا [Arabic]; tourteau de soja [French]; farelo de soja [Portuguese]; Соевый жмых [Russian]; Sojaextraktionsschrot [German]; 大豆粕 [Japanese]; chakula cha soya [Swahili]; soya küspesi [Turkish]; Bã đậu nành [Vietnamese]; 대두박 [Korean]; تفاله سویا [Persian]; Farina di estrazione di soia [Italian]; กากถั่วเหลือง [Thai]; Śruta poekstrakcyjna sojowa [Polish]; sójový extrahovaný šrot [Czech]; сојина сачма [Serbian]; sójový extrahovaný šrot [Slovak].

Synonyms 

Dolichos soja L., Glycine gracilis Skvortsov, Glycine hispida (Moench) Maxim., Glycine hispida var. brunnea Skvortsov, Glycine hispida var. lutea Skvortsov, Glycine soja (L.) Merr., Phaseolus max L., Soja hispida Moench, Soja max (L.) Piper

Description 

Soybean meal is the main protein co-product of soybean crushing and a widely used ingredient in compound feeds for livestock, poultry and aquaculture, particularly for omnivorous and herbivorous fish (Rojas et al., 2017; Glencross, 2023). Soybean meal is classified by crude protein content. High-protein meals, usually obtained from dehulled soybeans, contain 47–49% crude protein and about 3% crude fibre on an as-fed basis. Meals containing hulls or part of the hulls contain less than 47% crude protein and more than 6% crude fibre. Residual oil is typically below 2% in solvent-extracted meals and above 3% in mechanically extracted meals (Cromwell, 2012).

World soybean-meal production was 248.4 million tonnes in 2022/23, was estimated at 293.9 million tonnes in 2025/26 and is forecast to reach 302.4 million tonnes in 2026/27 (USDA FAS, 2026).

Regulatory and traceability considerations for genetically modified soybean material are discussed under Feed safety.

Alternatives to soybean meal

Despite its valuable nutritional attributes and widespread use in animal feeding, soybean meal raises supply-resilience concerns. In the European Union, for example, reliance on imported oilseed meals is a strategic-autonomy issue: in 2023/24, EU production covered 27% of its oilseed-meal needs (European Commission, 2024).

Potential alternatives to soybean meal include rapeseed meal, sunflower meal, cottonseed meal, peanut meal, maize distillers grains, pea seeds, faba beans, lupin seeds (blue lupin, yellow lupin, white lupin), sesame oil meal and palm kernel meal. The linked Feedipedia datasheets provide further information on each feed’s nutritional characteristics and use in animal feeding.

Dependency concerns may be addressed both by replacing part of soybean meal with other protein sources and by reducing its inclusion provided the diets still meet animals’ protein and amino acid requirements. Older practical guidance reported relatively high inclusion levels for several animal classes. As the species-specific comparisons below show, some of these historical figures exceed levels tested in recent studies, while others overlap; experimental diets describe the formulations tested, not current commercial practice (Ewing, 1997). The potential benefits of either approach depend on the ingredients used and their origin and production system.

Distribution 

Soybean meal is produced and traded worldwide. USDA FAS projections for 2026/27 put global trade at 90.1 million tonnes, with Argentina, Brazil and the United States leading exports (30.0, 27.1 and 20.6 million tonnes, respectively). The European Union is expected to remain the largest importer (20.4 million tonnes), followed by Indonesia (6.9 million tonnes) and Vietnam (6.5 million tonnes).

The same projections identify China, the United States, Brazil and Argentina as the main producers (87.9, 59.7, 50.0 and 33.5 million tonnes, respectively), and China, the United States, the European Union and Brazil as the largest domestic users (86.9, 40.0, 31.6 and 23.0 million tonnes, respectively). International supply also relies on whole-soybean imports for domestic crushing: China is expected to import 115.0 million tonnes and crush 111.0 million tonnes; the corresponding figures are 13.7 and 14.9 million tonnes for the European Union, and 6.8 and 7.0 million tonnes for Mexico. All figures are for the 2026/27 marketing year and come from the USDA PSD release of 9 October 2026 (USDA FAS, 2026).

Processes 

Soybean oil is extracted mainly by two methods: solvent extraction and mechanical pressing. Solvent extraction is the most efficient method, typically leaving less than 2% residual oil in the resulting soybean meal. Mechanical extraction includes conventional screw pressing (expelling) and processes combining extrusion and pressing (extruding/expelling). These methods are less efficient at recovering oil, generally leaving more than 3% residual oil in the resulting meals. They also differ in their processing conditions and in the characteristics of the resulting soybean meals (Johnson et al., 2018; Cheng et al., 2019).

Preparation of soybeans for oil extraction

Before oil extraction, soybeans are cleaned to remove foreign materials and cracked into smaller particles. The hulls may then be separated from the kernels (dehulling). As soybean hulls contain little oil and are mainly composed of fibre, their removal increases the protein concentration and reduces the fibre content of the resulting meal (Toomer et al., 2023).

For solvent extraction, the cracked soybeans are conditioned by heating and adjusting their moisture content, which increases their plasticity and facilitates flaking. The conditioned particles are then flattened between rollers to produce thin flakes. Flaking disrupts the cellular structure and increases the surface area accessible to the solvent, thereby improving oil extraction efficiency (Dunford, 2012; Toomer et al., 2023).

Solvent extraction

Before solvent extraction, the soybean flakes may be passed through an expander, which produces porous particles and facilitates oil extraction. This treatment can improve solvent percolation and reduce solvent consumption (Dunford, 2012).

The oil is extracted by percolation of a solvent, usually hexane, through a bed of flakes or expanded material. The solvent dissolves the oil, and the resulting oil-solvent mixture (miscella) is collected separately. Several alternative solvents have been investigated to reduce reliance on petroleum-derived hexane, including alcohols (ethanol and isopropanol), ethyl acetate, bio-based 2-methyloxolane (2-MeOx), cyclopentyl methyl ether (CPME) and terpenes. Although some of these solvents have shown promising oil extraction efficiencies, their industrial application depends on technical, economic, environmental and safety considerations, as well as on the quality of the resulting soybean meal (Gasparetto et al., 2022; Menoury et al., 2025).

After extraction, the spent flakes are desolventised, toasted, dried, cooled and ground to produce soybean meal. Desolventisation removes the extraction solvent, while thermal treatment reduces the activity of heat-sensitive antinutritional factors. These operations are commonly combined in industrial desolventiser-toaster equipment (Johnson et al., 2018).

The hulls removed before extraction may be added back to the meal to obtain products with different protein and fibre contents (Toomer et al., 2023).

Mechanical extraction

Screw pressing

In mechanical extraction, soybeans are generally cracked, conditioned by heating and fed into a screw press (expeller), where increasing pressure forces the oil out of the seed material. The resulting press cake is subsequently cooled and ground to produce soybean cake. Compared with solvent extraction, mechanical pressing generally recovers less oil, resulting in meals with higher residual oil contents and consequently higher energy values, but lower protein concentrations (Johnson et al., 2018; Cheng et al., 2019).

Heat is generated by friction and compression during pressing, but the temperature and duration of treatment vary according to the equipment and operating conditions. Consequently, mechanical pressing alone does not necessarily provide sufficient inactivation of heat-sensitive antinutritional factors, and additional thermal treatment may be required (Johnson et al., 2018).

Extruding/expelling

Extruding/expelling combines a preliminary extrusion step with subsequent mechanical oil extraction in a screw press. During extrusion, soybean material is subjected to high temperature, pressure and shear, which disrupt cellular structures and facilitate oil release during pressing. Extrusion can also contribute to the inactivation of heat-sensitive antinutritional factors. Compared with conventional screw pressing, this two-stage process can improve oil recovery (Cheng et al., 2019).

Mechanical extraction processes are used in facilities of various capacities, including small-scale processing units, and can be particularly relevant for local soybean processing and identity-preserved supply chains, such as non-GM or organic production (Johnson et al., 2018).

Heat treatment and antinutritional factors

Heat treatment is an essential step in soybean meal production, as raw soybeans contain antinutritional factors, particularly trypsin inhibitors and lectins, that can impair protein digestion and animal performance. These heat-sensitive compounds are largely inactivated by adequate thermal processing. In solvent-extracted soybean meal, this treatment is generally performed during desolventisation and toasting, whereas mechanically extracted soybean cakes may require specific heating treatments before or after pressing (Ruiz et al., 2020; Toomer et al., 2023).

The effectiveness of thermal processing depends on the combination of temperature, moisture and treatment duration. Insufficient heating leaves residual antinutritional activity, while excessive heating can reduce protein quality and amino acid availability, particularly lysine, through Maillard reactions (Ruiz et al., 2020; Toomer et al., 2023).

Several analytical methods are used to assess the adequacy of heat treatment. Urease activity is a traditional indicator of insufficient heating, although it does not directly measure trypsin inhibitor activity. Protein solubility in potassium hydroxide (KOH) and the protein dispersibility index (PDI) provide complementary information on the extent of protein denaturation and possible overheating. Direct measurement of trypsin inhibitor activity is particularly useful for evaluating residual antinutritional activity (Ruiz et al., 2020; Toomer et al., 2023).

Other antinutritional components, such as phytates and the oligosaccharides raffinose and stachyose, are less affected by conventional heat treatment and may require other processing methods to reduce their concentrations (Toomer et al., 2023).

Further processing

Fermentation

Beyond heat treatment, fermentation has attracted increasing interest for its potential to improve soybean meal’s nutritional properties and provide health benefits, including effects on oxidative status, immune responses and gut microbiota (Heuzé et al., 2025). Depending on the microorganisms and processing conditions, it can reduce some antinutritional components and increase small peptides and free amino acids; however, these changes do not seem to consistently improve nutrient digestibility or animal performance (Xue et al., 2024; Heuzé et al., 2025; Navarro et al., 2017).

Enzymatic treatments

Enzymatic treatments of soybean meal, particularly with carbohydrases and proteases, have been investigated to degrade non-starch polysaccharides and proteins that may limit nutrient utilisation. Their effects on the energy value and amino acid digestibility of soybean meal have been variable (Sotak et al., 2014; Navarro et al., 2017).

Fine grinding

Fine grinding reduces soybean meal particle size and increases the surface area available for digestive enzymes. In broilers, fine grinding of soybean meal and full-fat soybeans has been reported to improve ileal amino acid digestibility, with greater digestibility values observed for finely ground soybean meal than for full-fat soybeans (Valencia et al.,2009).

Environmental impact 

The environmental footprint of soybean depends on its origin, cultivation and processing practices, transport, and how impacts are allocated between oil and meal (Escobar et al., 2020; Puntigam et al., 2024).

Deforestation

Soybean expansion in South America has involved the conversion of native vegetation, including Amazon forest and Cerrado savannas. Much new cropland has also replaced existing pasture, rather than forest directly (Zalles et al., 2019). In the Brazilian Amazon, a study of municipalities subject to enhanced deforestation monitoring found that additional soybean expansion occurred mainly on pastures and other cropland, alongside reduced forest clearing (Damm et al., 2024). The Amazon Soy Moratorium, which excluded soy grown on land deforested after July 2008 from participating traders' supply chains, substantially reduced forest conversion in soy-suitable areas (Heilmayr et al., 2020). However, most traders terminated their commitments in early 2026; a scenario analysis estimated that the agreement's loss could lead to 1.4 million additional hectares of deforestation over the following decade compared with its continuation (Rausch et al., 2026).

Biodiversity

Conversion of native savannas to agriculture reduces and fragments wildlife habitat. A spatial assessment of the Cerrado identified agricultural land use as a major contributor to potential losses of native vertebrate diversity, although its estimates concern agriculture as a whole rather than soybeans alone (Rabeschini et al., 2025).

Greenhouse gas emissions

Land-use change can dominate the climate footprint of soy from recently cleared areas. In 2010-2015, emissions per tonne of soy equivalent from some Brazilian agricultural-frontier municipalities were up to six times the national average (Escobar et al., 2020). Cultivation inputs, transport and crushing also contribute emissions, while estimates for soybean meal depend on the allocation of shared impacts between oil and meal (Escobar et al., 2020; Puntigam et al., 2024).

Herbicides and resistant weeds

Herbicide-tolerant soybean cultivation has changed weed-control practices. In US soybean fields monitored during 1998-2011, glyphosate-tolerant soybean adopters applied on average 28% more herbicide by weight than non-adopters, although the difference was not significant when assessed using an environmental impact quotient. The increasing difference over time was consistent with glyphosate-resistant weeds (Perry et al., 2016).

Soil and water quality

Replacing pastures or native vegetation with soybean cropland can increase erosion and sediment runoff, depending on soil management and rainfall. In the Prata River basin in Brazil, rapid soybean expansion was associated with more days of severely turbid water, although rainfall remained the principal explanatory factor (Chiaravalloti et al., 2022).

Industrial processing

Crushing, solvent extraction and meal heat treatment require energy; solvent extraction also creates a risk of atmospheric n-hexane emissions. European technical guidance identifies solvent recovery and air-emission controls as important measures (Giner Santonja et al., 2019).

Mitigation strategies and sustainable production

Limiting further conversion of native vegetation can be supported by farm-level traceability, monitoring and effective enforcement. The Amazon Soy Moratorium cited above illustrated the value of coordinated deforestation-free sourcing backed by public monitoring, but its 2026 disruption highlighted the fragility of voluntary commitments (Heilmayr et al., 2020; Rausch et al., 2026). Certification schemes such as the Round Table on Responsible Soy (RTRS) and ProTerra promote land-use safeguards and improved farming practices; a study of 35 Cerrado farms observed generally good compliance but stressed the importance of verification. Crop rotations, reduced tillage and continuous soil cover can improve soil conservation (Angnes et al., 2025). In North American maize-soybean systems, modelling suggested that cover-crop management combined with earlier sowing of longer-maturing soybean varieties could reduce emissions from soybean production by 33% (Della Chiesa et al., 2024).

Mitigation in animal feeding

Excess dietary nitrogen is excreted and contributes to ammonia emissions from livestock manure (Cappelaere et al., 2021). In an experiment involving 192 grower-finisher pigs, diets combining soybean meal reduction or substitution with amino acid supplementation and reduced phosphorus supply decreased nitrogen excretion by up to 20% and phosphorus excretion by up to 25%, without significantly changing overall growth performance. Modelled acidification and global-warming impacts decreased by up to 14% and 7%, respectively, although the most protein-reduced and alternative-protein diets reduced carcass lean percentage (Puntigam et al., 2024).

Nutritional aspects
Nutritional attributes 

Soybean meal is a highly palatable, protein-rich feedstuff, containing 43–53% crude protein on an as-fed basis. Its amino acid profile is particularly valuable in cereal-based diets: it supplies highly digestible lysine, tryptophan, threonine and isoleucine, which are often limited in cereal grains. In monogastric diets, its digestible amino acids and high lysine content can allow lower total protein levels than with other protein sources, reducing excess nitrogen supply and excretion (Sauvant et al., 2004; Pettigrew et al., 2008). However, methionine and cystine concentrations are relatively low for monogastric animals, so the complete diet must provide adequate amounts of these amino acids, through supplementation where necessary (McDonald et al., 2002).

Soybean meal is also relatively rich in phosphorus, but about 60–70% is bound to phytate and poorly available to monogastric animals (Waldroup et al., 2008; Philippi et al., 2023).

Potential constraints 

Feed safety

Solvent residues

Hexane, the conventional solvent used for soybean oil extraction, is petroleum-derived and highly flammable. Its use raises occupational health concerns because n-hexane is neurotoxic, as well as environmental concerns related to solvent emissions. Most solvent is removed during desolventisation, although residues may remain in soybean meal. In a feeding study, traces of n-hexane were detected in milk from cows fed hexane-extracted soybean meal; concentrations were below the analytical limit of quantification, and the study did not establish adverse health effects (Menoury et al., 2025). In 2024, EFSA identified the need to reassess technical hexane used in food processing, considering its composition, impurities, residual exposure and toxicological properties (EFSA, 2024). These concerns have encouraged research into alternative extraction solvents.

Fungal contamination and mycotoxins

Soybean meal can be contaminated by toxigenic fungi and mycotoxins, particularly when post-harvest handling or storage is inadequate. Surveys of soy feed materials have detected aflatoxins, fumonisins, deoxynivalenol and zearalenone, although occurrence varies with the toxin, sample and region. Soybean meal appears less susceptible overall than maize, but contamination and the co-occurrence of toxins can still occur (Rodrigues et al., 2012; Gutleb et al., 2015; Li et al., 2022).

Regulatory considerations

Regulatory requirements for soybean meal differ across countries and regions, reflecting differences in regulatory frameworks, production systems and market requirements. These differences concern the control of chemical residues, manufacturing practices, product traceability and the use of genetically modified soybeans.

In the European Union, feed safety legislation addresses undesirable substances and chemical impurities arising from manufacturing processes and processing aids. Regulation (EU) No 68/2013, as amended, establishes provisions concerning such impurities in feed materials. The limits established for extraction solvents used in food production under Directive 2009/32/EC should not be directly applied to animal feed (European Commission, 2013; European Commission, 2022).

In the United States, the Food Safety Modernization Act (FSMA) emphasises hazard analysis and risk-based preventive controls in animal feed manufacturing facilities, including the identification and management of chemical hazards (FDA, 2017).

In Brazil, Decree No. 12,031/2024 establishes requirements for the inspection and control of animal feed products, including manufacturing conditions, authorised ingredients, quality control programmes and traceability (DOU, 2024).

Producers and users of soybean meal must therefore comply with the requirements applicable in their respective markets, particularly when products are traded internationally.

Genetically modified soybeans

Genetically modified (GM) soybeans are widely used in animal feeding, particularly those developed for herbicide tolerance or insect resistance. A GM event refers to a specific genetic modification in a plant, which may be present in several commercial varieties. Stacked events combine two or more GM events in the same plant.

The safety assessment of GM soybeans considers their composition, nutritional value, toxicity and allergenicity. Authorised GM soybean meals generally have nutritional characteristics comparable to those of conventional soybean meals, except when genetic modification is intended to alter their composition. However, regulations concerning authorisation, cultivation, traceability and labelling differ considerably between countries.

In the European Union, numerous GM soybean events are authorised for import and use in food and feed, but not for cultivation. Specific traceability and labelling requirements apply (European Parliament and Council, 2003a, European Parliament and Council, 2003b; European Commission, 2026).

In the United States, GM soybeans are regulated by the Food and Drug Administration (FDA) for food and feed safety, the Department of Agriculture (USDA) for plant health and the Environmental Protection Agency (EPA) for pesticidal traits (FDA, 2025).

In Brazil, the National Technical Biosafety Commission (CTNBio) assesses GM soybean events for commercial release, including cultivation and use in food and feed (Brazil, 2005; CTNBio, 2021).

In China, the Ministry of Agriculture and Rural Affairs (MARA) regulates GM soybean imports and domestic cultivation. China has authorised numerous GM soybean events for import and processing and has recently expanded approvals for domestic commercial cultivation (USDA FAS, 2025).

Variability

Soybean meal is generally considered a relatively consistent protein feed ingredient. However, its composition and nutritional quality vary according to soybean genetics, growing and harvesting conditions, geographical origin, storage and processing methods. Differences concern not only crude protein content but also amino acid composition, energy value and protein digestibility (Liu et al., 2024; Oviedo-Rondón et al., 2024).

Recent studies have confirmed differences in the nutritional value of commercial soybean meals from different origins. In particular, variations in amino acid digestibility and energy value have been reported among soybean meals produced in Argentina, Brazil and the United States. Because soybean meal is often included at high levels in animal diets, regular assessment of its composition and nutritional quality is important for accurate feed formulation (Oviedo-Rondón et al., 2024).

Antinutritional factors

Trypsin inhibitors and lectins

Soybean meal may contain residual antinutritional factors, particularly trypsin inhibitors and lectins, which can impair nutrient utilisation, especially in monogastric animals. Trypsin inhibitors reduce the activity of digestive proteases, thereby decreasing protein and amino acid digestibility and potentially affecting animal growth. Their residual activity depends largely on the adequacy of heat treatment (Ruiz et al., 2020; Toomer et al., 2023).

In broilers, soybean meal with lower trypsin inhibitor activity (1.8 vs. 4.8 mg/g) resulted in higher digestibility of dry matter, nitrogen, energy and amino acids (Dourado et al., 2011). More recent experiments have confirmed a negative relationship between trypsin inhibitor activity and amino acid digestibility in broiler chickens (Kuenz et al., 2022).

In pigs, increasing dietary trypsin inhibitor activity has been shown to reduce growth performance, feed efficiency, nitrogen digestibility and nitrogen retention, particularly in young animals (Nisley et al., 2025).

Other antinutritional components, including oligosaccharides and phytates, may also limit nutrient utilisation. Their effects are discussed separately below.

Goitrogens and oestrogens

Soybean meal contains isoflavones, mainly genistein and daidzein, which have phytoestrogenic properties. Their concentrations vary with soybean origin and processing conditions. Isoflavones can exert oestrogenic or anti-oestrogenic effects, with potential consequences for reproductive function and other physiological processes, depending on the animal species and level of exposure (Grgic et al., 2021).

Soy isoflavones may also interfere with thyroid function, particularly when dietary iodine supply is insufficient. In an early study, cows receiving soybean meal as a major supplementary protein source gave birth to calves with enlarged thyroid glands, an effect associated with inadequate iodine supplementation (Hemken et al., 1971). Adequate iodine nutrition is therefore important in preventing goitrogenic effects associated with soybean-based diets (Doerge et al., 2002).

Non-starch polysaccharides (NSP)

Soybean meal contains non-starch polysaccharides (NSP), including pectic polysaccharides, arabinogalactans, cellulose and hemicelluloses, whose concentrations depend partly on the proportion of hulls. NSP are poorly digested by endogenous enzymes in monogastric animals but can be fermented by intestinal microorganisms. Their effects on nutrient utilisation depend on their solubility and fermentability (Bach Knudsen, 1997; Choct et al., 2005).

Soybean meal also contains raffinose and stachyose, two oligosaccharides that are not NSP. They are fermented by intestinal microorganisms and may reduce the energy value of the meal. Low-oligosaccharide soybean meals have been shown to provide higher metabolizable energy values in roosters (Parsons et al., 2000).

Enzymes such as β-mannanases and α-galactosidases can improve nutrient utilisation in soybean meal-based diets, although the results are variable. β-Mannanase supplementation has shown beneficial effects on energy utilisation and feed efficiency in pigs and poultry (Kiarie et al., 2021), whereas Graham et al. (2002) found no improvement in growth performance despite substantial reductions in raffinose and stachyose.

Phytates and mineral availability

Phytates can also bind minerals, particularly zinc, and reduce their availability. Consequently, soybean meal-based diets may require mineral supplementation, depending on the composition of the complete diet (Waldroup et al., 2008; Philippi et al., 2023).

Supplementation with microbial phytases improves phosphorus digestibility in pigs and poultry, reduces the need for inorganic phosphorus supplementation and can decrease phosphorus excretion, thereby limiting its environmental impact. Phytate degradation may also improve the availability of other nutrients, although the response depends on dietary composition and phytase activity (Philippi et al., 2023; Valente Junior et al., 2024).

Ruminants 

Soybean meal is a widely used and palatable protein supplement for high producing dairy and beef cattle (McDonald et al., 1998; Rego et al., 2008; Krysl et al., 1989; Guthrie et al., 1988). More than 60% of its protein is degraded in the rumen, supporting microbial protein synthesis, while the fraction that escapes degradation can provide amino acids for absorption in the small intestine (INRA, 1988). Soybean meal also has a good amino acid balance and high cell wall digestibility (INRA, 1988). Studies have reported increased feed intake, milk yield or milk protein content in dairy cows (McDonald et al., 1998; Rego et al., 2008), and increased forage intake or nutrient digestibility in steers fed prairie diets (Krysl et al., 1989; Guthrie et al., 1988).

Responses depend on the basal ration and its protein supply: additional soybean meal may not improve production when protein requirements are already met and may increase nitrogen losses (Olmos Colmenero et al., 2006; Keller et al., 2022). Expeller meals retain more oil than solvent extracted meal and generally have higher energy value (Cromwell, 2012; Johnson et al., 2018). In the few trials assessing product quality, soybean meal was not associated with adverse changes in the milk or meat traits measured (Weiss et al., 2015; Menoury et al., 2026; Keller et al., 2021; Saro et al., 2019). Preruminant calves are considered separately because conventional soybean meal is not a straightforward substitute for milk proteins (Ansia et al., 2020; Burakowska et al., 2021).

Because much of soybean meal protein is degraded in the rumen, research has examined heat, mechanical and chemical treatments to increase its rumen undegraded protein (RUP) value and the amount of protein reaching the small intestine (Smith, 1986; Atwal et al., 1995; Wacyk et al., 2000; Chen KuenJaw et al., 2002; Colmenero et al., 2006; Castro et al., 2008).

Dairy cattle

Types of soybean meal and feeding value

Soybean meal can support milk production when it corrects a protein limitation in the ration (McDonald et al., 1998; Rego et al., 2008).

Conventional soybean meal

In grazing cows receiving maize silage, 1.4 kg soybean meal dry matter (DM)/cow/day, alongside 5.2 kg maize silage DM/cow/day, increased milk protein yield by 0.06 kg/cow/day in summer and autumn (McDonald et al., 1998).

In another grazing study, 6 kg concentrate/day containing 18% conventional soybean meal increased milk yield when grass silage was also fed, but not when cows grazed pasture alone; in the latter situation, soybean meal increased dietary nitrogen and feed cost without improving production (Rego et al., 2008).

In total mixed rations based on grass silage, increasing soybean meal from 5% to 10% or 15% of dietary DM formed part of a broader increase in crude protein. Milk and milk protein yields increased with dietary crude protein, but nitrogen use efficiency declined; responses were greater with treated canola meal than with conventional soybean meal (Gidlund et al., 2015).

More protein was not necessarily beneficial. In diets based on maize silage and supplemented with rumen protected methionine, diets containing 15% crude protein and 15% conventional soybean meal supported about 40 kg milk/cow/day, with lower nitrogen excretion than diets containing 17% crude protein and 19% soybean meal, without reducing milk or milk component yields (Nursoy et al., 2018).

Likewise, increasing solvent extracted soybean meal from 9.6% to 11.7% of dietary DM, alongside an increase in crude protein from 16.6% to 17.6%, did not increase milk yield and increased urinary nitrogen excretion by 54 g/day (Olmos Colmenero et al., 2006).

These studies show that soybean meal is a useful protein source, but not that it is always superior to other ingredients or that removing it necessarily reduces production (Doreau et al., 2014; Keller et al., 2022).

A ration containing 15% conventional soybean meal and 15% beet pulp produced more milk than one containing 30% dehydrated lucerne (26.0 vs. 24.1 kg/day); this comparison involved different ingredient combinations and does not isolate the effect of soybean meal (Doreau et al., 2014).

Expeller soybean meal

Expellers retain more oil than solvent extracted soybean meal and may provide more energy (Cromwell, 2012; Johnson et al., 2018).

However, a diet containing 4.6% solvent extracted and 5.9% expeller soybean meal did not sustain milk production as well as one containing 9.6% solvent extracted meal (Olmos Colmenero et al., 2006). Extruded soybean meal at 12% of dietary DM did not improve overall lactational performance and reduced milk protein yield (Harper et al., 2019).

Other soybean meals

In mid lactation cows, milk yields were similar with a diet containing 15.9% conventional soybean meal and diets containing either 11.2% conventional plus 4.4% heat treated soybean meal, or 11.6% conventional soybean meal plus 5.34% high protein distillers’ grains; all percentages are of dietary DM (Chesini et al., 2023).

In diets containing 16% conventional soybean meal, partly or fully replacing hexane extracted meal with 2 methyloxolane extracted meal did not change milk production or nitrogen utilisation (Menoury et al., 2025; Menoury et al., 2026).

Inclusion levels

The dairy cow trials cited here tested conventional soybean meal at 5–19% of dietary DM (Gidlund et al., 2015; Nursoy et al., 2018; Olmos Colmenero et al., 2006). Other studies used 15% of dietary DM with beet pulp (Doreau et al., 2014), 18% of a concentrate fed at 6 kg/day (Rego et al., 2008), or 1.4 kg DM/cow/day (McDonald et al., 1998). An earlier practical reference reported about 35% for dairy cows, above the levels tested in several recent studies (Ewing, 1997).

Beef cattle

Types of soybean meal and feeding value

Conventional soybean meal

Soybean meal can improve forage utilisation when protein is limiting. In Oklahoma, increasing soybean meal from 0 to 603 g DM/head/day increased forage intake and digestibility in heifers fed early cut prairie hay (Guthrie et al., 1988).

In New Mexico, 0.5 kg DM/head/day did not increase forage intake in steers grazing blue grama rangeland, but increased total tract organic matter and nitrogen digestibility (Krysl et al., 1989).

Its value also depends on the protein already supplied by the ration. In a forage based finishing diet that provided adequate metabolisable protein, omitting the additional protein supplement reduced urinary nitrogen excretion without affecting nitrogen or energy utilisation; methane emissions were similar to those from the conventional soybean meal diet (Keller et al., 2022).

Cold pressed soybean cake

Mechanically extracted cake retains more oil than solvent extracted soybean meal, so its energy value and feeding response depend on processing (Chipa et al., 2010).

In South Africa, young Nguni cattle received isonitrogenous feedlot diets containing 0%, 6%, 13% or 20% cold pressed soybean cake. Growth responses were best at 6–13%; 20% provided no additional benefit (Chipa et al., 2010).

Inclusion levels

In growing and finishing beef cattle diets, conventional soybean meal was included at 5.5–6.5% of dietary DM (Keller et al., 2021; Basiel et al., 2024). The 6.5% level was used in a maize based U.S. feedlot diet for beef × Holstein steers (Basiel et al., 2024).

In a 139 day U.S. feedlot trial, soybean meal replaced 50% or 100% of dried distillers grains with solubles initially included at 20% of dietary DM, corresponding to about 10% or 20% soybean meal. Full replacement increased final body weight but was associated with more severe liver abscesses (Ross et al., 2024). An earlier practical reference reported about 35% for beef cattle (Ewing, 1997).

Calves

Types of soybean meal and feeding value

Conventional soybean meal

Conventional soybean meal is a common protein source in solid calf starters and after weaning. In young calves receiving diets based on maize and soybean meal, methionine was identified as the first limiting amino acid, followed by lysine; responses to amino acid supplementation were less evident in older calves (Abe et al., 1998; Abe et al., 1999).

Conventional soybean meal is not a straightforward substitute for milk proteins in liquid feeds for preruminant calves. Residual trypsin inhibitors and antigenic proteins in inadequately treated soybean products can impair intestinal digestion and health (Ansia et al., 2020; Burakowska et al., 2021).

Fermented soybean meal

Fermentation can reduce antinutritional and antigenic constituents of soybean meal (Heuzé et al., 2025). In a Korean experiment, fermented soybean meal in starter feed increased body weight gain at four weeks (0.54 vs. 0.30 kg/day) and preweaning starter intake, although the advantage was not consistent at every age (Kim et al., 2012).

In a 9 week trial in Holstein calves reared in cold weather and abruptly weaned at 59 days, replacing one third or one half of the starter’s 27% conventional soybean meal with fermented meal (9% or 13.5% of starter DM) increased overall average daily gain (719 and 797 vs. 626 g/day). Feed intake and feed efficiency did not differ over the full trial, although both were higher in the fermented meal groups during the post weaning week (Rezazadeh et al., 2019).

Inclusion levels

A practical reference for calf concentrates is approximately 20% toasted soybean meal (Ewing, 1997). In trials with Holstein calves, conventional soybean meal accounted for 23% of starter DM or 24% of starter feed on an as fed basis (Senevirathne et al., 2017; Burakowska et al., 2021).

Sheep

Types of soybean meal and feeding value

Conventional soybean meal

Conventional soybean meal is used in supplementary concentrates for housed and grazing sheep during pregnancy, lactation and rapid growth. Its value depends on forage quality and animal requirements.

In Irish ewes, about 200 g/head/day in pregnancy diets based on maize silage improved ewe intake, weight and condition at lambing, increased lamb birth weight and reduced age at slaughter. Reducing soybean meal in high quality grass silage diets did not impair performance (Keady et al., 2021).

In Jordan, adding 125 or 250 g/day of conventional soybean meal to a low quality forage diet changed daily gain in Awassi lambs from −67 g/day without supplementation to 59 and 96 g/day, respectively; the two supplemented groups did not differ significantly (Obeidat et al., 2020).

In Spain, heavy Assaf lambs fed indoor finishing diets received 5.8–11.5% soybean meal as dietary crude protein increased from 13.4% to 17.3% of DM; daily gain increased from 221 to 297 g/day (Saro et al., 2020).

Inclusion levels

Across the trials reviewed, conventional soybean meal supply ranged from about 73 to 250 g/head/day in lambs and 179–200 g/head/day in ewes (Saro et al., 2020; Obeidat et al., 2020; Keady et al., 2021). Older practical guidance reported soybean meal at about 30% of dietary DM for ewes and 20% of dietary DM for lambs (Ewing, 1997).

Goats

Types of soybean meal and feeding value

Protein requirements in goats vary with physiological stage and production level; they are not uniformly low. Conventional soybean meal can supplement a ration when its protein supply is insufficient, with its contribution assessed against the animals’ needs and the whole diet (Sahlu et al., 2004).

Conventional soybean meal

In Italian dairy goats, replacing 250 g conventional soybean meal/head/day with the same amount of ground maize reduced dietary crude protein from 16% to 12.2% of DM. Milk yield and composition did not differ significantly, while nitrogen use efficiency increased from 28.0% to 37.2% and milk urea decreased (Rapetti et al., 2020).

In growing male Anhui white goat kids in China, a diet containing 20% conventional soybean meal on an as fed basis and 13.4% crude protein on a DM basis maintained growth, whereas a diet containing 16% soybean meal and 12.0% crude protein reduced growth performance. Soybean meal inclusion and dietary crude protein changed together in this comparison (Zhu et al., 2020).

Inclusion levels

The cited trials used 250 g conventional soybean meal/head/day in Italian dairy goats and 20% of complete feed on an as fed basis in growing male kids (Rapetti et al., 2020; Zhu et al., 2020).

Pigs 

Soybean meal is a major protein source in pig diets. Its digestible essential amino acids, particularly lysine, complement cereal grains, although methionine may need to be supplemented (McDonald et al., 2002). Its feeding value varies with origin, processing and residual oil content. In an evaluation of 23 soybean meals from five countries, digestible energy ranged from 15.95 to 17.32 MJ/kg DM among country means; higher insoluble dietary fibre and trypsin inhibitor activity were associated with lower digestible and metabolisable energy (Lopez et al., 2020). Processing must also be controlled: inadequate heating leaves trypsin inhibitors active, whereas excessive heating can reduce amino acid digestibility. Additional autoclaving at 125°C progressively reduced crude protein and amino acid digestibility in growing pigs (González-Vega et al., 2011).

Piglets

Types of soybean meal and feeding value

Conventional soybean meal

Soybean meal supplies protein and essential amino acids, but newly weaned piglets are more sensitive to soybean antigens and residual antinutritional factors. Glycinin and β-conglycinin are among the proteins of concern; allergenic β-conglycinin subunits have been identified in sensitised piglets (Zheng et al., 2014). Newly weaned pigs have also been reported to prefer dried milk products such as whey or skim milk (Patience et al., 1995).

Enzyme-treated soybean meal

In a 28 day study, diets containing 9% enzyme-treated and 12% conventional soybean meal during the first 14 days supported higher average daily gain than a control diet containing 24% conventional soybean meal. During the following 14 days, a diet containing 7.5% enzyme-treated and 12% conventional soybean meal had higher crude protein and gross energy digestibility than the conventional soybean meal control (Ma et al., 2019).

Fermented soybean meal

In weanling pigs, the standardised ileal digestibility of most amino acids was similar in conventional, fermented and enzyme-treated soybean meals. Differences in digestible amino acid concentrations reflected product composition rather than consistently higher digestibility of processed meals (Cervantes-Pahm et al., 2010).

Inclusion levels

In one trial, the conventional control diets contained 24% soybean meal during the first 14 days and 22% during the next 14 days (Ma et al., 2019). As an example of commercial practice, the PIC programme suggests maximum inclusions of 20% from weaning to approximately 7.5 kg body weight and 28% from approximately 7.5 to 11.5 kg. These are programme-specific guidelines (PIC, 2021). Older practical guidance reported about 20–25% for piglets (Ewing, 1997).

Growing and finishing pigs

High trypsin inhibitor activity can limit the feeding value of inadequately processed soybean ingredients. In a 27 day study in grower pigs with an initial body weight of 39.7 kg, increasing soybean-derived trypsin inhibitor activity from 0.99 to 9.38 TIU/mg of complete feed, by adding raw ground soybeans to soybean meal, linearly reduced average daily gain and feed efficiency. Nitrogen digestibility was also lower at 9.38 TIU/mg than at 0.99 and 2.23 TIU/mg (Miller et al., 2025b).

Types of soybean meal and feeding value

Conventional soybean meal

In a 49 day trial, diets containing 18–26% soybean meal initially and 12–19% in the final phase supported similar average daily gain; higher inclusions improved feed and caloric efficiency (Cemin et al., 2022). In late-finishing pigs in the United States, increasing soybean meal from 5% to 20% improved growth and feed efficiency, mostly between 5% and 8.75%. The response was small above 8% in diets containing 25% distillers’ grains, while growth and feed efficiency improved as soybean meal increased from 0% to 16% in diets containing 30% wheat middlings (Holen et al., 2023). In trials in Kansas and Minnesota, increasing soybean meal from 19.1% to 33.5% in maize-based grower diets improved average daily gain and gain-to-feed ratio; with 20% distillers’ grains, 18.2–34.3% supported similar growth. In late-finishing pigs, 9.5–23.2% supported similar growth and carcass characteristics (Faccin et al., 2026).

Older studies reported higher energy and lysine concentrations in dehulled than in non-dehulled soybean meal, as well as better feed conversion and performance from starter to finishing (Patience et al., 1995; Swick, 1997).

Expeller soybean meal

Dry extrusion and mechanical pressing retain more oil than solvent extraction and can provide more energy. In growing pigs, high-shear dry soybean expellers had higher digestibility for most amino acids and higher digestible, metabolisable and calculated net energy values than solvent-extracted soybean meal from the same batch of soybeans. The products were tested at 35% and 33% in the amino acid digestibility assay and at 32% and 30% in the energy assay, respectively (Rodriguez et al., 2020).

Fermented soybean meal

In finishing pigs in China, 7.42% fermented soybean meal was formulated to replace 50% of conventional soybean meal. Average daily gain and nutrient digestibility increased, while feed intake and feed-to-gain ratio were unchanged. Carcass weight and muscle antioxidant capacity also increased (Xie et al., 2022).

Inclusion levels

Recent trials tested conventional soybean meal at approximately 12–34% of complete grower diets and 0–23.2% of late-finishing diets in the United States; responses varied with diet formulation (Cemin et al., 2022; Holen et al., 2023; Faccin et al., 2026). In China, 7.42% fermented soybean meal was formulated to replace half of the conventional soybean meal (Xie et al., 2022). Older practical guidance reported about 30% for growing and finishing pigs (Ewing, 1997).

Sows

Types of soybean meal and feeding value

Conventional soybean meal

In China, 11 solvent-extracted soybean meals of different origins were tested at 25.5% of the diet in mid and late gestation. Their digestible and metabolisable energy values were similar; one dehulled Brazilian meal had higher nitrogen digestibility in late gestation (Wang et al., 2022). In another Chinese study, five soybean meals differing in origin and processing had net energy values of 11.1–12.7 MJ/kg DM (Xue et al., 2025).

In a United States lysine-response experiment, increasing lysine intake from diets containing 19.2–41.5% conventional soybean meal increased litter growth rate (Greiner et al., 2020). In Kansas, diets containing 25%, 30% or 35% soybean meal were formulated to the same standardised ileal digestible lysine concentration. Higher inclusion reduced sow feed intake, particularly at 35%, and increased sow weight loss, while litter growth and the weaning-to-oestrus interval did not differ (Gourley et al., 2020). In a commercial herd in Western Illinois where porcine reproductive and respiratory syndrome virus (PRRSv) was circulating, diets containing 20–35% soybean meal did not affect litter performance or mortality. Sows receiving 20% had higher feed intake and better body condition at weaning; feed efficiency was higher at greater inclusions, alongside lower feed intake (Johnson et al., 2025).

Fermented soybean meal

In China, sows received 2%, 4% or 6% fermented soybean meal, replacing the same amount of conventional soybean meal, from day 78 of gestation to day 21 of lactation. Piglet weights were higher at days 14 and 21, while litter size, survival at birth and birth weight were unchanged. Several sow serum markers of oxidative stress were lower (Luo et al., 2021).

Inclusion levels

Lactation trials tested conventional soybean meal at 20–35% in a commercial PRRSv-positive herd and at 25–35% in a controlled trial; feed intake declined as inclusion increased in the latter study (Gourley et al., 2020; Johnson et al., 2025). The PIC programme reports reduced feed intake above 30% (PIC, 2021), consistent with older practical guidance of about 30% for sows (Ewing, 1997). Fermented soybean meal was tested at 2–6%, replacing the same proportion of conventional soybean meal (Luo et al., 2021).

Poultry 

Properly processed soybean meal is a major protein source for poultry. Diets based on maize and soybean meal provide most essential amino acids, although methionine generally needs to be supplemented (Waldroup et al., 2008). In the United States, soybean meal supplies approximately 66% of the protein in broiler feeds (Dozier et al., 2011). Feeding value depends on meal composition and processing, and responses vary with bird species, age and diet.

Broilers

Types of soybean meal and feeding value

Conventional soybean meal

Soybean meal supports broiler growth when diets meet energy and digestible amino acid requirements. Residual trypsin inhibitors, lectins, antigenic proteins and oligosaccharides may affect nutrient utilisation and intestinal health; effects of oligosaccharides vary with dietary concentration and bird age (White et al., 2024).

Heat-treated soybean meal

Adequate heating inactivates heat-sensitive antinutritional factors, while insufficient or excessive heating can impair feeding value. Earlier broiler studies found better growth with heat-processed than raw soybean meal, but excessive heating reduced amino acid availability and performance (Parsons et al., 1991; Anderson-Hafermann et al., 1992; Araba et al., 1990; Tousi-Mojarrad et al., 2014). Extrusion temperature also mattered: soybean meals processed at 121–135°C were considered underprocessed in one study (Karr-Lilienthal et al., 2006). In a 21-day US trial, broilers fed approximately 32% adequately heat-treated soybean meal gained 52 g more than those fed underprocessed meal and had significantly better feed conversion (Bowen et al., 2025).

Dehulled soybean meal

Earlier work reported increased egg size and shell strength in hens fed dehulled soybean meal, as well as improved weight gain and gain-to-feed ratio in broilers (Park et al., 2002). In a European trial, extrusion-pressed or flaking-cooking-pressed meals, with or without dehulling, were included at 29–32% of starter diets and 25–29% of grower diets. Dehulling did not affect growth or feed conversion but increased carcass yield from approximately 65–67% to 69% (Sakkas et al., 2019; Royer et al., 2020).

Expeller-pressed and extruded soybean meals

In Benin, diets containing 28% locally processed soybean meal were compared. Broilers fed solvent-extracted meal had higher body weights at 21 and 49 days, better starter feed conversion and lower feed cost per kilogram of weight gain than birds fed expeller-pressed meal (Houndonougbo et al., 2008). In a 49-day trial, expeller-extruded meal supported growth similar to solvent-extracted meal, although breast-meat yield was lower (Powell et al., 2011). Another study found higher ileal amino acid digestibility, weight gain and feed intake, and better feed conversion with extruded soybean meal (Jahanian et al., 2016).

Extruded-expelled soybean meal from a high-amino-acid variety

In a US trial, extruded-expelled meals from conventional soybeans or a variety selected for higher amino acid content supported growth, feed efficiency and carcass yield similar to conventional solvent-extracted meal. The selected variety provided higher digestible amino acid concentrations and allowed soybean meal inclusion to be reduced by 1.3–1.8 percentage points without impairing performance (Wells et al., 2026).

Fermented soybean meal

In a Chinese trial with 336 broilers, replacing part of conventional soybean meal with 2.5–7.5% fermented soybean meal did not affect growth performance but improved some meat-quality traits. At 2.5–5%, breast-meat drip and cooking losses decreased, although leg-meat yield was also reduced. Fermented soybean meal also reduced breast-meat malondialdehyde content (Guo et al., 2020).

Soybean variety

In a 42-day South Korean trial, soybean meal from the Wonheug variety, included at 31% in starter diets and 27.1% in grower diets, improved weight gain, feed efficiency and breast- and leg-meat yields compared with commercial soybean meal. The Wonheug meal contained more crude protein (57.0 vs. 51.7%) and methionine (0.69 vs. 0.61%), contributing to differences in dietary composition (Yang et al., 2025).

Inclusion levels

Recent experiments included conventional soybean meal at approximately 28–39% of starter diets, 25–33% of grower diets and 23–29% of finisher diets, on an as-fed basis (Houndonougbo et al., 2008; Acar et al., 2024; Sakkas et al., 2019; Yang et al., 2025; Wells et al., 2026). Older practical references reported about 25% for chicks and 30–40% for broilers (Willis, 2003; McDonald et al., 2002; Ewing, 1997). Recent experimental levels overlap with these historical figures and vary by feeding phase.

Laying hens

Types of soybean meal and feeding value

Conventional soybean meal

In a German assessment of 18 soybean meals, standardised ileal lysine digestibility ranged from 85 to 92%, and nitrogen-corrected metabolisable energy from 7.5 to 10.5 MJ/kg DM. Differences associated with soybean origin were generally small or inconsistent (Siegert et al., 2023).

Dehulled soybean meal

Earlier work reported larger eggs and stronger shells in hens fed dehulled soybean meal (Park et al., 2002).

Expeller-pressed and extruded-expelled soybean meals

In a Canadian study, four expeller-pressed meals included at 29% of complete diets produced no significant differences in laying performance, feed conversion or measured egg-quality traits, despite variation in meal protein content (Neijat et al., 2024). In an eight-week trial, diets containing conventional solvent-extracted, extruded-expelled or full-fat soybean products at 21–25% of complete feed did not significantly affect laying performance or feed efficiency. Extruded-expelled defatted meal increased eggshell strength, while the high-oleic full-fat product increased egg oleic acid content by 52% compared with the conventional control (Toomer et al., 2024).

Fermented soybean meal

In a Chinese trial with 360 young Hy-Line Brown laying hens, diets containing 2.5–10% fermented soybean meal progressively replaced part of the approximately 26% conventional soybean meal in the control diet. Some egg-quality traits, including Haugh units and eggshell strength, improved, but responses varied with inclusion level and feeding duration; some treatments also increased abnormal or broken eggs (Obianwuna et al., 2024).

Inclusion levels

Recent control diets contained approximately 21–26% conventional soybean meal (Toomer et al., 2024; Obianwuna et al., 2024), below the former practical reference of about 30–40% for laying hens (Willis, 2003; McDonald et al., 2002; Ewing, 1997).

Ducks

Types of soybean meal and feeding value

Conventional soybean meal

In a South Korean digestibility study of three-week-old Pekin ducks, soybean meal had standardised ileal digestibility values of 89.4% for lysine, 93.6% for methionine and 86.5% for threonine; the processing type was not specified (Oketch et al., 2023). In a 35-day US trial, reducing metabolisable energy by 132 kcal/kg in maize–soybean meal diets lowered body weight and worsened feed conversion. Supplementation with a multi-carbohydrase enzyme complex at 75–125 ppm partly compensated for these changes, without adverse effects on carcass traits (Leyva-Jimenez et al., 2024).

Fermented soybean meal

In a 108-day trial with laying ducks, 1–3% fermented soybean meal was added to basal diets containing 21.2% conventional soybean meal during early lay and 10.5% during peak lay. Feed conversion and Haugh units improved, while some treatments increased the incidence of broken or soft-shelled eggs, particularly during peak lay at the highest supplementation level (Zhou et al., 2026).

Inclusion levels

In the laying-duck trial, basal diets contained 21.2% conventional soybean meal during early lay and 10.5% during peak lay; fermented soybean meal was added at 1–3% (Zhou et al., 2026). For practical guidance, example complete rations for duck farmers contain 18.2% soybean meal in starter, 19.7% in grower, 16.1% in finisher, and 12.4–14.0% in developer and layer diets. These are example formulations, not maximum inclusion levels (NC State Extension, 2020).

Turkeys

Types of soybean meal and feeding value

Heat-treated soybean meal

In US trials, severe overheating of soybean meal included at 40–49% of diets reduced weight gain and feed efficiency in young turkeys, whereas moderately increased heating did not impair performance. No adverse effects were observed in older birds fed diets containing 20–28% soybean meal (Lee et al., 1991).

Fermented soybean meal

In Poland, a 112-day trial in BIG 6 turkey hens found that 7% fermented soybean meal improved intestinal morphology and some immune and antioxidant indicators. Inclusions of 9% and 10% improved growth; at 10%, however, oxidative and inflammatory markers increased, as did some blood indicators related to liver and kidney function (Chachaj et al., 2019).

Inclusion levels

In a US trial with young turkeys, conventional soybean meal represented 46% of complete feed during days 1–14 and 45% during days 15–32, alongside 7.5% poultry meal; these levels supported satisfactory growth in the experimental control group (VerBeek et al., 2024).

Commercial feeding guidelines for heavy turkey lines set maximum soybean meal inclusions at 40% of the diet from 0 to 12 weeks and 15% from 13 to 21 weeks when soybean meal is the only soy product used (Aviagen Turkeys, Feeding Guidelines for Nicholas and B.U.T. Heavy Lines).

Rabbits 

Soybean meal is a concentrated source of protein and lysine but contributes little fibre. Its use in rabbit diets should therefore be considered alongside the fibre content of the complete diet (Lebas, 2004).

Types of soybean meal and feeding value

Conventional soybean meal

In growing rabbits, diets containing 7–11.5% soybean meal combined with increasing soluble fibre, from 5.8 to 8.5%, supplied by alfalfa meal and dried beet pulp, improved daily gain and feed conversion ratio (Trocino et al., 2010).

Enzymolytic soybean meal

In a 56-day trial with weaned Rex rabbits in China, enzymolytic soybean meal replaced 0.5, 1.0 or 1.5 percentage points of conventional soybean meal, while total soybean meal inclusion remained approximately 11%. Feed-to-gain ratio improved when 1.0 or 1.5 percentage points were replaced. Replacement of 0.5 percentage points increased full and half eviscerated slaughter ratios. Meat pH, colour, cooking loss and shear force were unchanged (Kong et al., 2022).

Inclusion levels

Earlier practical guidance placed toasted soybean meal at 15–20% of complete diets (Lebas, 2004). For small-scale home-mixed rabbit diets, protein concentrates such as soybean meal or sunflower meal were suggested at about 10% of the diet (NCAT, 2011). In a recent trial, enzymolytic soybean meal replaced 0.5–1.5 percentage points of conventional soybean meal while total soybean meal inclusion remained around 11% (Kong et al., 2022).

Horses and donkeys 

Horses

Types of soybean meal and feeding value

Conventional soybean meal

In Thoroughbred mares, soybean meal was fed at 0.10% of body weight per day before foaling and 0.15% during lactation. Milk protein content increased during the first five weeks of lactation. Their foals had higher plasma concentrations of several amino acids and gained more withers height over seven weeks (11.8 vs. 10.1 cm) (Glade et al., 1990).

In Leipzig, Germany, a short-term feeding trial with eight Warmblood geldings found that solvent-extracted soybean meal increased post-meal plasma lysine exposure compared with the control diet (Bockisch et al., 2023). In Italy, adding conventional soybean meal to a meadow-hay diet improved ration digestibility in six horses (De Marco et al., 2012).

Inclusion levels

Soybean meal was fed at 0.07% of body weight per day to geldings and at 0.10–0.15% to mares. In the Italian digestibility trial, it made up 20% of the as-fed ration with meadow hay (Bockisch et al., 2023; Glade et al., 1990; De Marco et al., 2012).

Donkeys

Types of soybean meal and feeding value

In China, a mobile-bag study in adult donkeys measured conventional soybean meal digestibility at 82.1% for dry matter and 96.3% for crude protein before the caecum, and 94.9% and 98.4%, respectively, over the total digestive tract (Liu et al., 2020b).

In a 120-day trial in Shandong, China, suckling Dezhou donkey foals received a formula containing 15% conventional soybean meal, 8% fermented soybean meal and 5% expanded soy product. Their final body weight and average daily gain were higher than with the milk-protein and mixed formulas: 125.1 kg and 722 g/day, compared with 115.3–116.1 kg and 659–666 g/day (P < 0.001). Feed conversion was 0.88, compared with 0.93 for the milk-protein formula, but did not differ significantly from the mixed formula (0.89) (Li et al., 2025).

Inclusion levels

In adult donkeys, conventional soybean meal was tested at 2.5–5.6% of dietary DM. In the foal trial, formulas contained 0%, 9% or 15% conventional soybean meal alongside fermented and expanded soy products (Liu et al., 2020a; Li et al., 2025).

Fish 

Because of its availability and cost, soybean meal has long been considered a relevant plant-protein alternative to fishmeal and is highly palatable to most warm-water fish (Brown et al., 2008; Lowell, 1998; Akiyama, 1991). Partial fishmeal replacement by soybean products has also been demonstrated in salmonids (Kaushik, 2008). However, responses vary among species and life stages: soybean meal has been associated with distal-intestinal enteritis in Atlantic salmon, whereas studies in other fish report both satisfactory performance and adverse responses, depending on the diet and inclusion level (Baeverfjord et al., 1996; Bakke-McKellep et al., 2007; Urán et al., 2009; Agboola et al., 2022).

Herbivorous fish

Grass carp (Ctenopharyngodon idella)

Types of soybean meal and feeding value

In China, diets containing 40 or 70% conventional soybean meal reduced growth and feed efficiency and caused intestinal inflammation; inflammation partly resolved at 40%, but persisted at 70% (Wu et al., 2018). In another Chinese trial, survival did not differ significantly across diets containing 0–30% conventional soybean meal. Replacing half of the 30% inclusion with Chlorella vulgaris improved weight gain and feed efficiency (Yang et al., 2023).

Inclusion levels

Survival was 87.3% at 30% soybean meal and remained similar at lower levels. Growth was impaired at 40 and 70% in a separate trial (Yang et al., 2023; Wu et al., 2018).

Omnivorous fish

Nile tilapia (Oreochromis niloticus)

Types of soybean meal and feeding value

In Ghana, expeller-pressed soybean meal at 32.5, 42.5 or 50.9% supported growth similar to a commercial fishmeal-based control and reduced feed costs, but shortened intestinal villi and reduced goblet-cell numbers (Obirikorang et al., 2020). In Brazil, 7% mixed-culture fermented soybean meal in a plant-based diet supported growth comparable to the fishmeal control; inclusions above 21% improved intestinal villus height, and 28% increased goblet-cell numbers (Picoli et al., 2022).

Inclusion levels

In the studies reviewed, levels around 25% were compatible with good growth, while intestinal effects reported at 32.5% and above warrant caution (Liu et al., 2020; Obirikorang et al., 2020). The fermented product was tested at 7, 14, 21 and 28%; 7% allowed complete fishmeal replacement without reducing growth in the tested formulation (Picoli et al., 2022).

Hybrid crucian carp (Carassius auratus gibelio ♀ × Cyprinus carpio ♂)

Types of soybean meal and feeding value

In China, increasing conventional soybean meal from 0 to 68% of dietary DM, replacing 0–100% of fishmeal, reduced growth and feed utilisation at the higher levels and adversely affected digestive, intestinal and immune indicators (Liu et al., 2020). Around 26% of dietary DM was compatible with good growth (Liu et al., 2020).

Carnivorous fish

Atlantic salmon (Salmo salar)

Types of soybean meal and feeding value

Responses vary with life stage and trial conditions. In the Netherlands, 300-g salmon fed 10 or 20% conventional soybean meal developed distal-intestinal enteritis; lesions appeared earlier at 20% (Urán et al., 2009). In Norway, enteropathy was also reported in post-smolts fed 25% dehulled, solvent-extracted soybean meal (Bakke-McKellep et al., 2007). More recent Norwegian and US trials reported mild inflammation with 20% in seawater salmon and significant distal enteritis with 40% in freshwater juveniles (Djordjevic et al., 2021; Tsai et al., 2023). By contrast, Norwegian fry fed 16.7% from first feeding showed no inflammation up to 144 days post-hatch (Sahlmann et al., 2015). A review of 26 studies found that enteritis severity varied with production phase, feed, inclusion level, year and water temperature (Agboola et al., 2022).

Inclusion levels

Inflammation was reported at 10–40% in several salmon trials, while one fry trial reported no inflammation at 16.7%; findings varied with life stage and trial conditions (Urán et al., 2009; Bakke-McKellep et al., 2007; Djordjevic et al., 2021; Tsai et al., 2023; Sahlmann et al., 2015).

Rainbow trout (Oncorhynchus mykiss)

Types of soybean meal and feeding value

In a US trial, diets containing 8 or 16% conventional or enzyme-treated soybean meal all produced lower growth than the fishmeal control, although the enzyme-treated meal performed better than conventional meal at both levels (Kumar et al., 2020). In Germany, complete fishmeal replacement with 50% conventional soybean meal impaired growth and feed conversion and was associated with intestinal inflammation (Seibel et al., 2022).

Inclusion levels

Complete fishmeal replacement was not achieved without reduced performance. The trials tested 8 and 16% conventional or enzyme-treated meal, and 16.4, 33 and 50% conventional meal (Kumar et al., 2020; Seibel et al., 2022).

Hybrid snakehead (Channa argus × Channa maculata)

In China, a diet containing 12% conventional and 7.2% fermented soybean meal supported growth, feed utilisation and intestinal health similar to a fishmeal control. Increasing fermented meal to 14.4% or more while reducing fishmeal reduced growth (Duan et al., 2022).

Largemouth bass (Micropterus salmoides)

In China, conventional soybean meal at 24.5% and 40.9% of the diet increased feed conversion ratio and reduced weight gain, respectively. Fermented meal at 15.7%, with 8% conventional meal, maintained growth; increasing fermented meal to 31.4% reduced it (He et al., 2020). In another Chinese trial, 10% fermented meal replacing 12% conventional meal maintained growth, while 20% fermented meal replacing 12% conventional meal and 8% maize gluten meal increased weight gain by 11.8% (Guo et al., 2023).

Crustaceans 

Soybean meal has been used in marine shrimp feeds for decades. Combined with other plant protein sources, it has contributed to the development of fishmeal-free diets, although the results depend on the species and the overall formulation (Akiyama, 1991; Amaya et al., 2008). The studies reviewed here concern Pacific white shrimp, mud crab and abalone; their findings do not establish a common inclusion level for these animals and should not be generalised to other molluscs, such as mussels or oysters.

Pacific white shrimp (Litopenaeus vannamei)

Reported inclusion levels are not directly comparable: trials used different fishmeal baselines and shrimp sizes. In Thailand, shrimp initially weighing 1.72–1.79 g grew more on diets containing 23.5 or 38% conventional soybean meal than on a control diet containing 27.5% fishmeal; the 38% diet was also associated with midgut and hepatopancreas changes (Kasamechotchung et al., 2025). In China, shrimp initially weighing about 3 g maintained growth with 3% conventional meal replacing 17% of fishmeal protein; 6–9% reduced growth and feed efficiency. Fermented meal supported replacement up to 33%, but not 50% (Yao et al., 2020). In South Korea, shrimp initially weighing 0.65 g maintained growth with conventional or fermented meal replacing 20–40% of fishmeal over seven weeks; fermented meal better maintained superoxide dismutase activity at the higher replacement level (Bae et al., 2020).

Mud crab (Scylla paramamosain)

In Vietnam, conventional soybean meal included at 30% had apparent digestibility values of 87.6% for DM, 98.4% for crude protein and 95.6% for gross energy (Truong et al., 2009). In Indonesia, a trial with juvenile crabs initially weighing 0.65 g found that replacing 20% of fishmeal protein with soybean protein supported growth; the 40% replacement treatment was less satisfactory (Suwirya et al., 2009). Because these experiments addressed different outcomes, no practical inclusion level can be established.

Other species 

Abalone (Haliotis discus hannai)

In molluscs, evidence mainly concerns abalone and should not be generalised to mussels or oysters. In South Korea, a diet containing 58% conventional soybean meal as a complete replacement for fishmeal supported survival, but growth was higher with a mixed diet containing 29% soybean meal and 16% silkworm pupae meal (Cho, 2010). In China, enzyme-treated soybean meal replaced up to 75% of fishmeal without reducing weight gain over 100 days; complete replacement impaired digestive-gland and antioxidant indicators (Yu et al., 2022).

Inclusion levels. The 58% conventional soybean-meal diet did not produce the best growth among the tested formulations (Cho, 2010). For enzyme-treated soybean meal, replacement of 75% of fishmeal corresponded to 18.3% of the diet and did not reduce weight gain (Yu et al., 2022).

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 88 0.8 86.3 95.9 1259  
Crude protein % DM 55.2 1.6 48.9 58.5 1372  
Crude fibre % DM 4.4 0.6 1.6 5.7 382  
Neutral detergent fibre % DM 10.5 1.7 6.2 12.1 19 *
Acid detergent fibre % DM 5.7 1.2 3.6 8.1 11 *
Lignin % DM 0.4 0.3 0.1 1.2 25  
Ether extract % DM 1.7 0.6 0.4 3.8 1130  
Ash % DM 7.3 0.5 6.1 9.2 315  
Insoluble ash % DM 0.07 0.05 0.01 0.2 8  
Starch (polarimetry) % DM 6.3 1.5 3.4 9.9 40  
Starch (enzymatic) % DM 1.1   0.4 2.1 3  
Total sugars % DM 10.8 1 8.6 12.4 29  
Gross energy MJ/kg DM 19.7 0.3 19.2 20.8 20 *
               
Amino acids Unit Avg SD Min Max Nb  
Alanine g/16g N 4.3 0.3 3.8 5.8 89 *
Arginine g/16g N 7.3 0.5 6 9.1 90 *
Aspartic acid g/16g N 11.3 0.6 9 14.1 87 *
Cystine g/16g N 1.6 0.1 0.8 1.7 93 *
Glutamic acid g/16g N 17.9 1 15 21.7 87 *
Glycine g/16g N 4.2 0.2 3.8 4.9 89 *
Histidine g/16g N 2.7 0.2 2.4 3.2 80 *
Isoleucine g/16g N 4.6 0.2 3.8 5.1 81 *
Leucine g/16g N 7.7 0.4 6.5 8.7 86 *
Lysine g/16g N 6.2 0.3 5.2 7 164 *
Methionine g/16g N 1.4 0.1 1 1.6 115 *
Methionine+cystine g/16g N 3 0.2 1.8 3.1 93 *
Phenylalanine g/16g N 5.1 0.2 4.4 5.7 91 *
Phenylalanine+tyrosine g/16g N 8.6 0.5 7.7 10.1 71 *
Proline g/16g N 5 0.3 4.5 6.2 45 *
Serine g/16g N 4.6 0.4 4.2 6.1 91 *
Threonine g/16g N 3.8 0.3 3.4 4.6 92 *
Tryptophan g/16g N 1.4 0.07 1.1 1.4 52 *
Tyrosine g/16g N 3.5 0.3 2.9 4.4 72 *
Valine g/16g N 4.8 0.3 4.1 5.8 89 *
               
Fatty acids Unit Avg SD Min Max Nb  
Myristic acid C14:0 % fatty acids 0.2 0.3 0 1.1 14  
Palmitic acid C16:0 % fatty acids 11.2 2.2 9.6 20.8 22  
Palmitoleic acid C16:1 % fatty acids 0.1 0.08 0 0.2 7  
Stearic acid C18:0 % fatty acids 3.8 0.4 3.2 4.8 22  
Oleic acid C18:1 % fatty acids 23.1 1.6 19.8 27.3 23  
Linoleic acid C18:2 % fatty acids 54 2.9 42.9 58.2 22  
Linolenic acid C18:3 % fatty acids 7.2 0.9 4.8 8.7 22  
               
Minerals Unit Avg SD Min Max Nb  
Calcium g/kg DM 3.9 0.7 2 6 359 *
Phosphorus g/kg DM 7.1 0.6 5.7 8.9 362 *
Potassium g/kg DM 24.3         *
Sodium g/kg DM 0.13 0.18 0.01 0.61 24  
Chlorine g/kg DM 1 1 0.4 3.2 7  
Magnesium g/kg DM 3.2 0.3 3 3.9 7 *
Sulfur g/kg DM 4.6 0.3 4.4 5.1 6  
Manganese mg/kg DM 44 12 25 75 10  
Zinc mg/kg DM 57 11 45 77 9  
Copper mg/kg DM 17 1 15 19 8  
Iron mg/kg DM 201          
Selenium mg/kg DM 0.5   0.4 0.5 2  
               
Pig nutritive values Unit Avg SD Min Max Nb  
Energy digestibility, growing pig % 87.5       1 *
DE growing pig MJ/kg DM 17.3       1 *
MEn growing pig MJ/kg DM 15.8         *
NE growing pig MJ/kg DM 9.8         *
Nitrogen digestibility, growing pig % 90.1       1 *
               
Poultry nutritive values Unit Avg SD Min Max Nb  
AMEn cockerel MJ/kg DM 11.4         *
AMEn broiler MJ/kg DM 11.2         *
               
Ruminants nutritive values Unit Avg SD Min Max Nb  
OM digestibility, ruminants % 91.1       1 *
Energy digestibility, ruminants % 91.6       1 *
ME ruminants MJ/kg DM 13.4         *
Nitrogen digestibility, ruminants % 80.2         *
Nitrogen degradability (effective, k=6%) % 63       1 *
Nitrogen degradability (effective, k=4%) % 71         *
a (N) % 13       1  
b (N) % 85       1  
c (N) h-1 0.085       1  
Dry matter degradability (effective, k=6%) % 67       1 *
Dry matter degradability (effective, k=4%) % 73       1 *
a (DM) % 26       1  
b (DM) % 71       1  
c (DM) h-1 0.08       1  
               
Rabbit nutritive values Unit Avg SD Min Max Nb  
DE rabbit MJ/kg DM 17.2         *
MEn rabbit MJ/kg DM 15         *
Energy digestibility, rabbit % 87.1         *
Nitrogen digestibility, rabbit % 79.9         *

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

References

Adamidou et al., 2009; ADAS, 1988; Adedokun et al., 2008; Adedokun et al., 2014; AFZ, 2017; Anon., 2001; Barrows et al., 2015; Bourdon et al., 1980; Bourdon et al., 1982; Bourdon et al., 1984; Bryden et al., 2009; Carré et al., 1986; Cave, 1988; CIRAD, 1991; CIRAD, 2008; Coca-Sinova et al., 2008; Dadalt, 2015; Dale et al., 1985; Dewar, 1967; Eeckhout et al., 1994; Frikha et al., 2012; Garcia et al., 2007; Huang et al., 2006; Jacobsen et al., 1997; Jongbloed et al., 1990; Kong et al., 2013; Macgregor et al., 1978; Marty et al., 1993; Maupetit et al., 1992; Michalet-Doreau et al., 1985; Mondal et al., 2008; Muscato et al., 1981; NAS, 1982; Parsons et al., 1981; Perez et al., 1981; Perez et al., 1984; Ravindran et al., 1994; Ravindran et al., 2006; St-Hilaire et al., 2007; Szczurek, 2009; Urbaityte et al., 2009

Last updated on 10/30/2026 12:52:54

Main analysis Unit Avg SD Min Max Nb  
Dry matter % as fed 88 0.7 80.1 96.3 9654  
Crude protein % DM 52.6 1.1 43.8 58.4 9722  
Crude fibre % DM 6.8 0.7 4.8 10.7 3328  
Neutral detergent fibre % DM 14.2 2.9 6.6 19.5 269 *
Acid detergent fibre % DM 8.4 2.3 3.4 14.8 238 *
Lignin % DM 0.6 0.4 0.1 1.8 213  
Ether extract % DM 1.8 0.5 0.3 5.5 7801  
Ash % DM 7.1 0.6 5.7 11.2 2899  
Insoluble ash % DM 0.6 0.5 0 2.4 72  
Starch (polarimetry) % DM 5.7 1.4 0.2 11.4 367  
Starch (enzymatic) % DM 1.9   1.4 2.7 4  
Total sugars % DM 9.2 1 7.2 13.7 211  
Gross energy MJ/kg DM 19.7 0.6 17 22.6 136 *
               
Amino acids Unit Avg SD Min Max Nb  
Alanine g/16g N 4.4 0.2 3.7 5.6 151 *
Arginine g/16g N 7.3 0.3 6.2 8.3 154 *
Aspartic acid g/16g N 11.3 0.4 9.6 12.8 139 *
Cystine g/16g N 1.6 0.08 1.2 1.9 147 *
Glutamic acid g/16g N 17.8 0.5 15.2 18.9 147 *
Glycine g/16g N 4.2 0.1 3.8 4.8 150 *
Histidine g/16g N 2.7 0.1 2.3 3 158 *
Isoleucine g/16g N 4.6 0.2 3.6 5.2 158 *
Leucine g/16g N 7.6 0.2 7.1 8.3 156 *
Lysine g/16g N 6.2 0.2 5.3 7 212 *
Methionine g/16g N 1.4 0.06 1 1.5 155 *
Methionine+cystine g/16g N 3 0.1 2.3 3.6 147 *
Phenylalanine g/16g N 5.1 0.1 4.5 5.6 156 *
Phenylalanine+tyrosine g/16g N 8.6 0.2 7.8 9.7 114 *
Proline g/16g N 5 0.2 4.4 5.7 142 *
Serine g/16g N 4.7 0.2 3.9 6 148 *
Threonine g/16g N 3.8 0.1 3.3 4.5 156 *
Tryptophan g/16g N 1.4 0.04 1.2 1.5 123 *
Tyrosine g/16g N 3.5 0.1 3.1 4.1 117 *
Valine g/16g N 4.8 0.2 4.4 5.6 156 *
               
Fatty acids Unit Avg SD Min Max Nb  
Myristic acid C14:0 % fatty acids 0.2 0.3 0 1.1 14  
Palmitic acid C16:0 % fatty acids 11.2 2.2 9.6 20.8 22  
Palmitoleic acid C16:1 % fatty acids 0.1 0.08 0 0.2 7  
Stearic acid C18:0 % fatty acids 3.8 0.4 3.2 4.8 22  
Oleic acid C18:1 % fatty acids 23.1 1.6 19.8 27.3 23  
Linoleic acid C18:2 % fatty acids 54 2.9 42.9 58.2 22  
Linolenic acid C18:3 % fatty acids 7.2 0.9 4.8 8.7 22  
               
Minerals Unit Avg SD Min Max Nb  
Calcium g/kg DM 3.8 0.9 1.6 7.9 1729 *
Phosphorus g/kg DM 7.1 0.6 4.4 8.1 47 *
Potassium g/kg DM 23.8 1.4 20.9 28.6 76 *
Sodium g/kg DM 0.16 0.25 0 1.49 275  
Chlorine g/kg DM 0.3 0.2 0.1 0.9 95  
Magnesium g/kg DM 3.1 0.4 2.5 4.1 21 *
Sulfur g/kg DM 4.5 0.2 4.3 4.9 5  
Manganese mg/kg DM 45 13 25 88 66  
Zinc mg/kg DM 62 39 29 303 43  
Copper mg/kg DM 19 7 7 61 44  
Iron mg/kg DM 274 166 13 617 18  
Selenium mg/kg DM 0.2          
               
Pig nutritive values Unit Avg SD Min Max Nb  
Energy digestibility, growing pig % 85 4.7 72.5 97.7 28 *
DE growing pig MJ/kg DM 16.8 1.1 14.6 20.7 34 *
MEn growing pig MJ/kg DM 15.3         *
NE growing pig MJ/kg DM 9.4         *
Nitrogen digestibility, growing pig % 86.7 3.9 78.8 94.2 24 *
               
Poultry nutritive values Unit Avg SD Min Max Nb  
AMEn cockerel MJ/kg DM 10.9 1.4 9.1 16.5 24 *
AMEn broiler MJ/kg DM 10.7   9.4 11.1 4 *
               
Ruminants nutritive values Unit Avg SD Min Max Nb  
OM digestibility, ruminants % 90.3   86 91.8 3 *
Energy digestibility, ruminants % 90.7         *
ME ruminants MJ/kg DM 13.3         *
Nitrogen digestibility, ruminants % 80.2       1 *
Nitrogen degradability (effective, k=6%) % 63 10 45 93 39 *
Nitrogen degradability (effective, k=4%) % 71   63 86 4 *
a (N) % 13       1  
b (N) % 85       1  
c (N) h-1 0.085       1  
Dry matter degradability (effective, k=6%) % 67 17 40 98 14 *
Dry matter degradability (effective, k=4%) % 73   72 85 4 *
a (DM) % 26 10 5 47 12  
b (DM) % 71 11 52 93 12  
c (DM) h-1 0.08 0.047 0.017 0.151 12  
               
Rabbit nutritive values Unit Avg SD Min Max Nb  
DE rabbit MJ/kg DM 16.4       1 *
MEn rabbit MJ/kg DM 14.2         *
Energy digestibility, rabbit % 83.1       1 *
Nitrogen digestibility, rabbit % 82.8       1 *

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

References

Abdu Ali Mussa et al., 2016; ADAS, 1988; Adeola, 2003; AFZ, 2017; Aguilera et al., 1992; Agunbiade et al., 1992; Akinleye et al., 2012; Allan et al., 2000; Anon., 2001; Arieli et al., 1989; Arnaud et al., 2005; Aufrère et al., 1988; Aufrère et al., 1991; Bach Knudsen, 1997; Baidoo et al., 1987; Barbour et al., 1991; Barnett et al., 1981; Barrows et al., 2015; Batajoo et al., 1998; Batterham et al., 1984; Batterham et al., 1989; Batterham et al., 1990; Batterham, 1979; Baumgärtel et al., 2007; Bell et al., 1993; Beran et al., 2005; Bochi-Brum et al., 1999; Bootwalla, 2009; Borgeson et al., 2006; Bryan et al., 2019; Bryden et al., 2009; Bui Huy Nhu Phuc, 2006; Burgoon et al., 1991; Burr et al., 2011; Cappellozza et al., 2012; Chhay Ty et al., 2007; Christodoulou et al., 2005; Christodoulou et al., 2006; Chumpawadee et al., 2005; Church et al., 1982; CIRAD, 1991; CIRAD, 1994; CIRAD, 2008; Clark et al., 1993; Coca-Sinova et al., 2008; Costa et al., 2010; Da et al., 2013; De Boever et al., 1984; De Boever et al., 1994; De Silva et al., 1990; Demarquilly, 1987; Donkoh et al., 2009; Dust et al., 2005; Eeckhout et al., 1994; Eeckhout, 1980; El Zubeir et al., 1992; Erdman et al., 1987; Fan et al., 1995; Fekete et al., 1986; Fialho et al., 1995; Foltyn et al., 2015; Fondevila et al., 1994; Frikha et al., 2012; Getachew et al., 2004; Gilaverte et al., 2011; Gowda et al., 2004; Green et al., 1989; Guedes et al., 1996; Guillaume, 1978; Guimaraes et al., 2008; Habib et al., 2013; Haddad et al., 2000; Hadjipanayiotou, 2002; Hajen et al., 1993; Henderson et al., 1984; Horani et al., 1975; Huhtanen et al., 1988; Hurtaud et al., 2007; Huston et al., 1971; Israelsen et al., 1978; Jagadi et al., 1987; Jondreville et al., 1991; Jongbloed et al., 1990; Kan et al., 1988; Kandylis et al., 1986; Karlsson et al., 2009; Karunajeewa et al., 1987; Khandaker et al., 1996; Kuan et al., 1982; Kumar et al., 2007; Lawrence, 1978; Le Dividich et al., 1975; Lechevestrier, 1996; Lee et al., 2016; Lekule et al., 1990; Lessire et al., 2009; Lessire, 1990; Li et al., 2013; Lima et al., 2013; Lindberg et al., 1982; Lindberg, 1981; Lindberg, 1981; Livingstone et al., 1977; Lund et al., 2006; Mancuso, 1996; Mantysaari et al., 1989; May et al., 1971; Mohamed et al., 1988; Montero-Lagunes et al., 2011; Moreira et al., 2002; Morgan et al., 1984; Morse et al., 1992; Mustafa et al., 1997; Muztar et al., 1981; Nadeem et al., 2005; Nehring et al., 1963; Noblet et al., 1997; Noblet, 2001; Noftsger et al., 2000; Nouri-Emamzadeh et al., 2008; Nwokolo et al., 1976; Okine et al., 2005; Oksbjerg et al., 1988; Orskov et al., 1992; O'Shea et al., 1986; Partanen, 1994; Polan et al., 1985; Qiao ShiYan et al., 2004; Refstie et al., 1999; Saki et al., 2008; Schöne et al., 1996; Selle et al., 2003; Sharma et al., 1980; Shi et al., 1993; Soliva et al., 2005; Soren et al., 2009; Storey et al., 1982; Stutts et al., 1988; Sullivan et al., 1989; Swanek et al., 2001; Thacker et al., 2007; Tiwari et al., 2006; Todorov et al., 2016; Treviño et al., 2000; Valencia et al.., 2009; Van Cauwenberghe et al., 1996; Velez et al., 1991; Vérité et al., 1990; Vermorel, 1973; Vervaeke et al., 1989; Visitpanich et al., 1985; Wainman et al., 1984; Wang Dun et al., 2005; Weiss et al., 1989; Whitehead et al., 1982; Wiryawan, 1997; Wiseman et al., 1992; Wohlt et al., 1991; Woods et al., 1999; Woods et al., 2003; Yin et al., 1993; Zhu et al., 1990; Zongo et al., 1993; Zuprizal; Larbier et al., 1991

Last updated on 10/30/2026 12:56:15

Main analysis Unit Avg SD Min Max Nb  
Dry matter % as fed 87.7 0.9 85.1 93.5 803  
Crude protein % DM 49.5 1.7 44.1 54.9 818  
Crude fibre % DM 7.2 0.9 4.9 11.2 589  
Neutral detergent fibre % DM 14.8 2.3 10.9 20.7 38 *
Acid detergent fibre % DM 8.9 2.2 7.6 15.2 39 *
Lignin % DM 0.8 0.5 0.3 2.1 25  
Ether extract % DM 1.9 0.6 0.6 5.1 603  
Ash % DM 7.4 0.7 5.8 10 216  
Insoluble ash % DM 0.3 0.3 0.03 0.8 5  
Starch (polarimetry) % DM 6.8 1.3 5.2 9.7 20  
Starch (enzymatic) % DM 0.9   0.8 1.1 4  
Total sugars % DM 10.6 1.2 8.3 12.6 20  
Gross energy MJ/kg DM 19.5 0.6 17.8 20.8 16 *
               
Amino acids Unit Avg SD Min Max Nb  
Alanine g/16g N 4.4 0.4 3.6 5.3 46 *
Arginine g/16g N 7.3 0.4 6 8.2 49 *
Aspartic acid g/16g N 11.3 0.6 10 12.9 47 *
Cystine g/16g N 1.5 0.1 1.1 1.6 35 *
Glutamic acid g/16g N 17.8 1.4 14.4 23.3 48 *
Glycine g/16g N 4.2 0.2 3.4 4.8 46 *
Histidine g/16g N 2.7 0.2 2.3 3.1 31 *
Isoleucine g/16g N 4.6 0.4 4.2 6.1 32 *
Leucine g/16g N 7.6 0.4 6.4 8.6 36 *
Lysine g/16g N 6.2 0.3 5.6 6.6 52 *
Methionine g/16g N 1.4 0.2 1.1 1.8 45 *
Methionine+cystine g/16g N 3 0.2 2.5 3.3 35 *
Phenylalanine g/16g N 5.1 0.2 4.5 5.5 49 *
Phenylalanine+tyrosine g/16g N 8.6 0.4 7.7 9.6 24 *
Proline g/16g N 5 0.3 4.5 5.7 13 *
Serine g/16g N 4.8 0.3 4.4 5.5 46 *
Threonine g/16g N 3.9 0.2 3.4 4.5 49 *
Tryptophan g/16g N 1.4 0.05 1.3 1.4 20 *
Tyrosine g/16g N 3.5 0.3 3.1 4.3 24 *
Valine g/16g N 4.8 0.3 4.2 5.5 49 *
               
Fatty acids Unit Avg SD Min Max Nb  
Myristic acid C14:0 % fatty acids 0.2 0.3 0 1.1 14  
Palmitic acid C16:0 % fatty acids 11.2 2.2 9.6 20.8 22  
Palmitoleic acid C16:1 % fatty acids 0.1 0.08 0 0.2 7  
Stearic acid C18:0 % fatty acids 3.8 0.4 3.2 4.8 22  
Oleic acid C18:1 % fatty acids 23.1 1.6 19.8 27.3 23  
Linoleic acid C18:2 % fatty acids 54 2.9 42.9 58.2 22  
Linolenic acid C18:3 % fatty acids 7.2 0.9 4.8 8.7 22  
               
Minerals Unit Avg SD Min Max Nb  
Calcium g/kg DM 3.9 1.1 1.7 7.4 61 *
Phosphorus g/kg DM 7.1 0.6 6.2 9.1 60 *
Potassium g/kg DM 24.5 1.3 22.4 27 17 *
Sodium g/kg DM 0.09 0.08 0 0.2 26  
Chlorine g/kg DM 0.5 0.2 0.4 0.9 7  
Magnesium g/kg DM 3.3 0.3 2.4 3.4 10 *
Sulfur g/kg DM 4.5          
Manganese mg/kg DM 36 11 23 53 9  
Zinc mg/kg DM 41 8 28 48 5  
Copper mg/kg DM 16   12 18 4  
Iron mg/kg DM 274          
Selenium mg/kg DM 0.2          
               
Pig nutritive values Unit Avg SD Min Max Nb  
Energy digestibility, growing pig % 84.6         *
DE growing pig MJ/kg DM 16.5         *
MEn growing pig MJ/kg DM 15.1       1 *
NE growing pig MJ/kg DM 9.4         *
Nitrogen digestibility, growing pig % 86.1         *
               
Poultry nutritive values Unit Avg SD Min Max Nb  
AMEn cockerel MJ/kg DM 10.8         *
AMEn broiler MJ/kg DM 10.6         *
               
Ruminants nutritive values Unit Avg SD Min Max Nb  
OM digestibility, ruminants % 90.2         *
Energy digestibility, ruminants % 90.2 3.3 86 97 8 *
ME ruminants MJ/kg DM 13.2 0.5 13 14.5 8 *
Nitrogen digestibility, ruminants % 80.1         *
Nitrogen degradability (effective, k=6%) % 63 8 56 77 5 *
Nitrogen degradability (effective, k=4%) % 71         *
a (N) % 13       1  
b (N) % 85       1  
c (N) h-1 0.085       1  
Dry matter degradability (effective, k=6%) % 67   56 75 4 *
Dry matter degradability (effective, k=4%) % 73       1 *
a (DM) % 26   23 27 3  
b (DM) % 71          
c (DM) h-1 0.08   0.06 0.147 3  
               
Rabbit nutritive values Unit Avg SD Min Max Nb  
DE rabbit MJ/kg DM 15.9   14.9 18.4 2 *
MEn rabbit MJ/kg DM 13.8         *
Energy digestibility, rabbit % 81.3   76.2 90 2 *
Nitrogen digestibility, rabbit % 83.7   79.4 89.7 2 *

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

References

ADAS, 1991; AFZ, 2017; Agunbiade et al., 2004; Alcalde et al., 2011; Al-Marzooqi et al., 2015; Anon., 2001; Brestenský et al., 2013; Bryden et al., 2009; Chiou et al., 1995; CIRAD, 1991; CIRAD, 2008; Eeckhout et al., 1994; Ezequiel et al., 1999; Fagbenro et al., 2004; Goes et al., 2010; Henry et al., 1973; Lebas et al., 2012; Maertens et al., 1985; Maupetit et al., 1992; Oliveira et al., 2007; Park et al., 2017; Pastuszewska et al., 1974; Promkot et al., 2003; Rudolph et al., 1983; Voris et al., 1940; Wainman et al., 1984

Last updated on 10/30/2026 12:57:25

Main analysis Unit Avg SD Min Max Nb  
Dry matter % as fed 93.2 2.1 85.2 97.7 601  
Crude protein % DM 47 2.3 38.4 53.1 583  
Crude fibre % DM 6.4 1.1 2.9 11.1 444  
Neutral detergent fibre % DM 13.6 4.6 9.8 21.7 6 *
Acid detergent fibre % DM 8 2 5.8 11.7 7 *
Lignin % DM 0.8 0.6 0.1 1.8 7  
Ether extract % DM 9.5 2.5 5.8 21.3 292  
Ash % DM 6.6 0.5 5.6 8.8 201  
Insoluble ash % DM 0.7       1  
Starch (polarimetry) % DM 5 2.7 1 8.9 13  
Starch (enzymatic) % DM 0.8          
Total sugars % DM 9.3   8.8 9.7 3  
Gross energy MJ/kg DM 21.1 0.4 20.2 21.5 6 *
               
Amino acids Unit Avg SD Min Max Nb  
Alanine g/16g N 4.4 0.2 3.8 4.4 21 *
Arginine g/16g N 7.3 0.4 6.4 8.3 22 *
Aspartic acid g/16g N 11.2 0.7 10.4 12.8 11 *
Cystine g/16g N 1.5 0.2 1.1 1.8 22 *
Glutamic acid g/16g N 17.8 1 15.2 19.4 21 *
Glycine g/16g N 4.2 0.1 4 4.4 20 *
Histidine g/16g N 2.7 0.1 2.4 3 21 *
Isoleucine g/16g N 4.6 0.3 4.1 5.1 23 *
Leucine g/16g N 7.6 0.2 7.2 8.1 24 *
Lysine g/16g N 6.2 0.4 4.9 6.9 77 *
Methionine g/16g N 1.4 0.2 1 1.7 34 *
Methionine+cystine g/16g N 3 0.2 2.2 3.3 16 *
Phenylalanine g/16g N 5.1 0.2 4.8 5.4 22 *
Phenylalanine+tyrosine g/16g N 8.6 0.2 8.4 9.1 12 *
Proline g/16g N 5 0.4 4.4 6.6 21 *
Serine g/16g N 4.9 0.6 3.8 5.6 18 *
Threonine g/16g N 3.9 0.2 3.5 4.4 23 *
Tryptophan g/16g N 1.3 0.2 0.8 1.5 13 *
Tyrosine g/16g N 3.5 0.2 3.5 4.2 16 *
Valine g/16g N 4.8 0.3 4.2 5.3 12 *
               
Fatty acids Unit Avg SD Min Max Nb  
Myristic acid C14:0 % fatty acids 0.2 0.3 0 1.1 14  
Palmitic acid C16:0 % fatty acids 11.2 2.2 9.6 20.8 22  
Palmitoleic acid C16:1 % fatty acids 0.1 0.08 0 0.2 7  
Stearic acid C18:0 % fatty acids 3.8 0.4 3.2 4.8 22  
Oleic acid C18:1 % fatty acids 23.1 1.6 19.8 27.3 23  
Linoleic acid C18:2 % fatty acids 54 2.9 42.9 58.2 22  
Linolenic acid C18:3 % fatty acids 7.2 0.9 4.8 8.7 22  
               
Minerals Unit Avg SD Min Max Nb  
Calcium g/kg DM 3.7 1.1 1.3 5.2 18 *
Phosphorus g/kg DM 6.9 0.7 6 8.2 24 *
Potassium g/kg DM 22.4 2.6 15.2 24.6 23 *
Sodium g/kg DM 0.11 0.08 0 0.22 5  
Chlorine g/kg DM 0.3          
Magnesium g/kg DM 2.9 0.4 2.6 3.5 5 *
Sulfur g/kg DM 3.2   2.6 3.8 2  
Manganese mg/kg DM 37   32 42 2  
Zinc mg/kg DM 52   34 69 2  
Copper mg/kg DM 18   13 23 2  
Iron mg/kg DM 280   129 465 3  
Selenium mg/kg DM 0.2       1  
               
Pig nutritive values Unit Avg SD Min Max Nb  
Energy digestibility, growing pig % 85.4         *
DE growing pig MJ/kg DM 18.1         *
MEn growing pig MJ/kg DM 16.7         *
NE growing pig MJ/kg DM 11         *
Nitrogen digestibility, growing pig % 87.3       1 *
               
Poultry nutritive values Unit Avg SD Min Max Nb  
AMEn cockerel MJ/kg DM 12.8   12.6 13.8 2 *
AMEn broiler MJ/kg DM 12.2   10.7 13 3 *
               
Ruminants nutritive values Unit Avg SD Min Max Nb  
OM digestibility, ruminants % 88.2         *
Energy digestibility, ruminants % 89.2         *
ME ruminants MJ/kg DM 14.3         *
Nitrogen digestibility, ruminants % 79.5       1 *
Nitrogen degradability (effective, k=6%) % 63   47 83 2 *
Nitrogen degradability (effective, k=4%) % 71       1 *
a (N) % 13       1  
b (N) % 85       1  
c (N) h-1 0.085       1  
Dry matter degradability (effective, k=6%) % 67       1 *
Dry matter degradability (effective, k=4%) % 73         *
a (DM) % 26 10 5 47 12  
b (DM) % 71 11 52 93 12  
c (DM) h-1 0.08       1  
               
Rabbit nutritive values Unit Avg SD Min Max Nb  
DE rabbit MJ/kg DM 16.9         *
MEn rabbit MJ/kg DM 14.9         *
Energy digestibility, rabbit % 80         *
Nitrogen digestibility, rabbit % 85.1         *

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

References

Adewolu et al., 2010; AFZ, 2017; Albar, 2006; Alegbeleye et al., 2012; Allan et al., 2000; Balogun et al., 1990; Beran et al., 2005; Broderick et al., 1990; Broderick et al., 2002; CIRAD, 1991; CIRAD, 2008; Gupta et al., 2011; Holm, 1971; Jacob et al., 2008; Lim Han Kuo, 1967; Mjoun et al., 2010; Mlay et al., 2006; Mutayoba et al., 2011; Neumark, 1970; Nguyen Nhut Xuan Dung et al., 2002; Oluyemi et al., 1976; Pozy et al., 1996; Ravindran et al., 1994; Sécalibio, 2018; Tesfaye et al., 2013; Valaja et al., 1994; Yaakugh et al., 1994; Yamazaki et al., 1988

Last updated on 10/30/2026 13:05:17

References
References 
Datasheet citation 

Heuzé V., Tran G., Kaushik S., 2026. Soybean meal. Feedipedia, a programme by INRAE, CIRAD, AFZ and FAO. https://feedipedia.org/node/674 Last updated on October 30, 2026, 20:18

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