Research Summaries: Canola and Peas in Livestock Diets

Intoduction/Table of Contents

II. The Use ofCanola in Ruminant Diets

L. S. Ellwood M.Sc.

Introduction

Canola is a crop well suited for the use in ruminant diets. This paper reviews the literature published since 1980 pertaining to the use of canola products in ruminant diets. Canola is a very important part in the feeding of ruminants and there are many different canola products available. Supplementing ruminant diets with canola may result in improved human nutrition as well. The following sections discuss how inclusion rates, digestibility (rumen and total tract) and feeding innovations can be used to enhance nutritional value of canola in ruminant rations. Emphasis has been placed on Canadian and North American studies, although results from around the world have also been included.

Canola Meal

Chemical composition of Canola Meal

Canola is the common name used to identify two plants species, Brassica napus and B. campestris, that have developed by Canadian plant breeders from its predecessor rapeseed. Rapeseed meal (RSM), unlike canola meal (CM) usually contains high glucosinolate (50-100 mol/kg) and erucic acid (25-45% of rape oil) concentrations. Canola meal (CM) is obtained from the whole seed after removing oil by a direct solvent or prepress solvent extraction process. Canola oil contains less than 2% erucic acid. Canola meal must contain a minimum of 35% crude protein (CP), a maximum of 12% crude fiber (CF), and a maximum of 30 mol GL/gram (AAFCO 1992 as cited by Price et al. 1993 {918}). The removal of oil from canola seed concentrates the remaining ingredients, namely fiber and protein. Canola meal has been reported to contain 38.3% CP, 21.5% neutral detergent fiber (NDF), 17.5% acid detergent fiber (ADF), 12% CF, 3.6% ether extract (EE), 0.6% Ca, 1.0% P and 0.9% sulfur (S) (Bell 1993 {907}; Bell and Keith 1991 {972}) (table N-1). The estimated gross energy (GE) values for CM and soybean meal (SBM) were 18.64 and 20.07 MJ/kg. A typical metabolizable energy (ME) value used in cattle diets is 12.1 MJ/kg DM. In comparison to SBM, CM contains less GE, less protein and over three times as much fiber. However, CM is richer in most B-vitamins and essential minerals (Table N-5, N-6) (Bell 1993 {907}). Canola meal is higher in the sulfur amino acids (AA) and SBM is higher in lysine (Parker 1992; Bell and Keith 1991 {972}) (table N-2).

Protein

Protein is the main nutrient in CM (table 1). A comparison of protein fractions of common protein supplements are shown in table 1. Composition of CM is similar to SBM however, true protein (73%) of CM consists of rapid (15.3%), intermediate (79.2%) and slowly degradable (5.5%) protein fractions and SBM contains less rapid and slowly degradable protein (0.5 and 3.5%, respectively) and more intermediately degradable protein 86.0% (Van Soest and Fox 1992). Because CM and SBM both contain small amounts of slowly degradable protein most of the protein will be degraded in the rumen.
Table 1. Protein fractions of common protein supplements.
CMSBM CSMSunflower mealBrewers grains
CP (CP)42.349.0 45.625.926.0
Non-protein nitrogenz 21.011.08.011.0 3.0
Available true proteinz73.087.084.0 81.083.0
Unavailable Proteinz 6.02.08.0 5.012.0

z% of CP.
Van Soest and Fox (1992).

Canola meal protein is more soluble than SBM (table 2). The variation in CM and SBM protein solubility was measured by Christensen et al. (1998) on 11 separate CM purchases and 4 SBM purchases. The CP solubility ranged from 14.6 to 29% for CM and 7.8 to 21.3% for SBM. Fiems et al. (1985 {1193}) compared five batches of RSM and SBM and the average protein solubility was 40.7% and 18.9%, respectively. The amount of protein associated with NDF and ADF is higher in CM than SBM (table 2). This is due to the seed hulls (30% of the oil-free meal) remaining with the canola meal after processing. Levels of neutral detergent insoluble CP ranged from 8.4-16.8% and levels of acid detergent insoluble CP ranged from 5.1-6.7% (Moshtaghi Nia and Ingalls 1992 {937}, McAllister et al. 1993 {928}, McKinnon et al. 1995 as cited by Mustafa (1996); Mustafa et al. 1996 {2061}).
Table 2. Protein fractions of canola and soybean meal.
Protein FractionCMSBM
CP (%)42.349.0
Soluble CP (% CP)32.0 20.0
Non-protein nitrogen (% CP)21.0 11.0
Neutral detergent insoluble CP (% CP)11.0 5.0
Acid detergent insoluble CP (% CP)6.0 2.0

Van Soest and Fox (1992).

Fiber

The first limiting factor in CM inclusion in diets is energy availability (Bell 1993 {907}). The low DE and ME values of CM are due to the high fiber levels caused by the hull remaining with the meal (30% of oil free meal). Canola meal has three times more crude fiber (12.1%) compared to SBM (3.4%) (Bell 1993 {907}). Canola meal contains 13.1% crude fiber, 23.4% NDF and 19.1% ADF (Bell and Keith 1991 {972}). Another study by Khorasani et al. (1994 {858}) reported that CM contained 30.3% NDF, 20.9% ADF, 8.3% acid detergent lignin (ADL) and 12.6% cellulose. Fiber values for CM are higher than soybean and solvent extracted linseed meal. The NDF, ADF, and ADL values for soybean and linseed meal were 8.5, 4.6, and 0.2% and 25.9, 14.6 and 5.8%, respectively (Khorasani et al. 1994 {858}).

Energy

As previously mentioned, the relatively low energy value of CM is associated with the high fiber levels and is considered the limiting factor in CM usage (Bell 1993 {1232}). However, fiber digestion is less of a problem for ruminants than monogastrics and the available energy from CM is usually higher for ruminants. Gross energy (GE) of CM averages 4.4 0.2 Mcal/kg (Bell and Keith 1991 {972}) or ranges from 13.39 to 17.57 MJ/kg DM (Bell 1984 {1232}; NRC 1989; Zinn {884}). Zinn (1993 {884}) reported a DE of 4.12 Mcal/kg for CM and 4.57 Mcal/kg for SBM. Variation in GE content of CM is due to differences in lipid, protein and fiber contents (Bell 1984 {1232}).

Glucosinolates (GL)

Canola meal quality has increased with the development of low GL varieties (Bell 1993 {907}). The GL content is much lower in CM than RSM, 30 vs. 90 to 140 mol/g (Fiems et al. 1985 {1193}; Lardy and Kerley 1994 {851}) and is no longer the main limiting factor in CM usage. Canola meal contains less GL than whole canola seed (WCS) due to the thermal degradation during processing. Bell and Keith (1991 {972}) reported a wide variation in GL destruction, 15 to 77% among different crushing plants resulting in GL values of 6.8 to 33.7 mol/g. Cattle have a higher tolerance to GL products in comparison to monogastric animals (Subuh et al. 1995 {843}). Heifers fed 300g/kg of HG (60.7 mmol/g) or LG (29.0 mmol/g) RSM reported that the rumen was the principal site of GL breakdown and that the liver was mildly damaged by hydrolyzed products, mainly isothiocyanates (SCN). Glucosinolates are broken down into SCN, thiocyanates and nitriles (VanEtten and Tookey 1983 as cited by Lardy and Kerley 1994 {851}). When GL are hydrolyzed the thiocyanate ion is released, this prevents iodination and activation of thyroid hormones leading to hypothyroidism (Guyton 1986 as cited by Lardy and Kerley 1994 {851}; Bell 1984 {1232}). Thyroid activity of fast growing, young calves may be affected by smaller amounts of goitrogenic chemicals than adult cattle (Claypool et al 1985 {1181}). Glucosinolates have a pungent flavor (Fenwick et al. 1983 as cited by Lardy and Kerley 1994 {851}) and reduce palatability (Hill 1991 {996}). Some studies confirm an increase in calf feed intake (FI) with the use of low GL varieties (Stedman and Hill 1987 {1139}; Mawson et al. 1993 {922}).

Processes that Reduce the Glucosinolate Content

Many methods have been used to reduce GL content of increasing RSM value (Stedman and Hill 1987 {1139}; Lardy and Kerley 1994 {851}; Fenwick et al. 1986 as cited by Rhee 1993 {887}). These include heat + ammonia, steam, steam + ammonia, calcium hydroxide + ammonia and ammonia + extrusion. Most of these processes significantly reduced the GL content of RSM. Extrusion reduced the GL content by 75% (from 118 to 28 mol/g), but only steam alone reported a significant increase in FI in calves (Stedman and Hill 1987 {1139}; Lardy and Kerley 1994 {851}; Liang et al. 1993 {906}). Palatability was not increased (except with steam alone) with the reduction in GL. The lack of response was attributed to the remaining GL or their degradation products, nitriles, thiocyanates and isothiocyanates (Lardy and Kerley 1994 {851}). Slominski and Campell (1987 as cited by Stedman and Hill 1987 {1139}) demonstrated that there is little decomposition of GL with a dry heat (100 C), but decomposition occurs with a moist heat. Moist heat treatment at 127 C for 15 min reduced total GL concentration from 19.07 to 0.78 mol/g DM. Moist heat treatment decreased total and individual GL content increasing grass silage intake in Finnish Ayrshire bulls (Aronen and Vanhatalo 1992 {948}). The decrease was due to the thermal decomposition of the GL.


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