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Xie, Meng, Cui, and Ren: Effect of Cattle Breed on Meat Quality, Muscle Fiber Characteristics, Lipid Oxidation and Fatty Acids in China


The objective was to compare meat quality, muscle fiber characteristics, lipid oxidation and fatty acids of Limousin (LIM), Simmtental (SIM), Luxi (LX), Qinchuan (QC) and Jinnan (JN) offered the same diet in China. After finishing, eight bulls from each breed were randomly selected for slaughter at 18.5 months old. Longissimus dorsi (ld) muscle was taken from the carcass for meat quality evaluations. Breed had little effect on most of meat and fat color parameters except for Hue and b* in which QC had lower values. LIM showed higher pH (24 h) and better water holding capacity than other breeds. LIM showed the lowest dry matter content but the highest crude protein. LX and LIM had higher percentage and density of red muscle fiber than other breeds. Lipid oxidations were significantly lower in LIM than in QC, with the LX, SIM and JN having the intermediate values. Compared to other four breeds, QC provided the highest values of polyunsaturated fatty acids (PUFA), n-6 fatty acids and n-3 fatty acids. In conclusion, LIM scored better on most of meat quality characteristics; however, local breeds such as LX and QC also had better muscle fiber characteristics and better fatty acids composition.


Breed is an important factor that can influence meat quality in some ways including muscle structure and meat physiology (Sañudo et al., 2004; Waritthitham et al., 2010). Though local breeds have some advantage such as crude feed tolerance, high reproductive performance, low maintenance requirements, their growth performance and dressing percentage are low (Liu et al., 2006; Li et al., 2009). To improve growth performance and meat quality, China has imported some high producing cattle breeds such as Limousin and Simmental from other countries. Zhou et al. (2001) reported that crossbreeding could significantly improve Yellow Cattle meat productivity. Yang et al. (2007) also noted that the growth performance and carcass quality of Limousin×Qinchuan crossbreed F1 cattle were improved under local conditions. Luxi, Qinchuan, Jinnan, Limousin and Simmental are the most important local and imported cattle breeds in China. However, no information is available comparing the meat quality of these cattle breeds based on the same age and feed resources.
The objective of this study was to compare meat quality characteristics of the imported breeds (Limousin and Simmtental) and local breeds (Luxi, Qinchuan and Jinnan) at the same age offered the same diet in China.


Animals and experimental design

The experiment was conducted at China Agricultural University Beef Cattle Practical Education Base located in Daxing District, Beijing. Fifteen male calves of Limousin (LIM), Simmental (SIM), Qinchuan (QC) and thirteen male calves of Luxi (LX) and Jinnan (JN) born in around December 2007 were selected and transferred to the experimental base at 6 months old. After arriving in the experimental base, all the bulls were fed maize stalk silage, by-products such as soybean pomace and brewers dried grain and concentrate ad libitum until about 15 months. Management practices were applied equally to all calves. At the commencement of the finishing trail the weight of the bulls ranged from 236 kg to 387 kg. Then all bulls were divided randomly into five breed groups and housed individually in stalls. During 105-d fattening period, the animals had the same total mixed ration ad libitum. The finishing period diet consisted of 440 g maize, 30 g cotton seed meal, 88 g soybean pomace, 110 g brewers dried grain, 300 g maize stalk silage and 32 g compound premix per kg dry matter. The nutrients composition were 11.1 metabolic energy MJ, 117 g crude protein, 400 g neutral detergent fiber, 196 g acid detergent fiber, 5.1 g Ca, 3.0 g P per kg dry matter. All procedures involving animals were conducted under approval of the China Agricultural University Institutional Animal Care and Use Committee.

Sampling procedures

Eight finished bulls selected randomly from each breed were slaughtered. Carcasses were chilled at 1 to 4°C for 24 h. To determine meat pH, Subcutaneous fat and muscle color, texture, chemical composition, lipid oxidations, and fatty acid composition, the longissimus dorsi (ld) of each left half side was cut between the 12th and 13th rib, dissected, and sliced into steaks.

Meat quality analysis

Measurement of pH was recorded in ld muscle at the 12th rib level with a pH meter (Eutech Instruments, pH Spear, USA). Subcutaneous fat color and muscle color were estimated between 12 and 13 ribs after 1 h blooming at 4°C using a portable colorimeter (Minolta, CR400/410, Japan) based on L*, a*, b* in the CIELAB space. Chroma (C*) and hue (h*) were calculated from the a* and b* values as:
C*=(a*×a*+b*×b*)1/2and h*=arctan b*/a*
One steak was cut into two blocks measuring 15×15×30 mm and then suspended at 4°C for 48 h to calculate drip loss. Another steak was vacuum packed in a polyethylene bag and heated at 80°C until the internal temperature reached 70°C to calculate the cooking loss percentage. Then each sample provided six round strips (1 cm diameter) for Warner-Bratzler Shear Force (Salter Brecknell, Model 2356X, USA) test and the fiber paralleled to the longest dimension.

Meat chemical composition analysis

A 50 g sample of ld was freeze dried for the determination of dry matter (DM), protein, fat and ash contents using standard procedures (AOAC, 1985).

Muscle fiber characteristics investigation

The fresh steak was cut into cubes of 1 cm3 and stored at −80°C for muscle fiber characteristics investigation. The nitro-blue tetrazolium technique was used to demonstrate succinic dehydrogenase activity situated in the mitochondria (Gauthier, 1969). Fibers were classified into red, intermediate and white according to the intensity of the staining reaction. The muscle fiber type percentage, muscle fiber diameter, and muscle fiber density were determined by digital camera (Nikon, TE2000-S, Japan) and Image Pro-plus analysis software.

Lipid oxidation determination

One steak about 20 g was homogenized and then stored at −80°C for lipid oxidation determination. The homogenized meat was taken out and then stored at 4°C with air exposure. Meat samples were collected at 0, 4, 8, 12, 24, 48 and 72 h for lipid oxidation determination.
Lipid oxidations were evaluated by the production of lipid hydroperoxides (PV) and thiobarbituric acid reactive substances (TBARS) according to the method of Richards and Dettmann (2003).

Determination of PV

Approximately 0.3 g of the tissue was homogenized in 5 ml of cold chloroform:methanol (1:1). Then 3.08 ml of cold 0.5% NaCl was added to separate the mixture into two phases. The mixture was then centrifuged at 3,297g (Beckman, J6M, USA) for 6 min at 4°C. Two ml of the lower chloroform layer was removed and transferred to a tube using a glass syringe and 1.33 ml of chloroform:methanol (1:1) was added to the 2 ml sample. Then 25 μl of 3.94 mol/L ammonium thiocyanate and 25 μl of 18 mmol/L iron (II) chloride were added to the tube, vortexing 4s after each addition. The sample was then incubated at room temperature for 20 min and absorbance read at 500 nm (Keda, UV8500, China). A standard curve was constructed using cumene hydroperoxide and the concentration of lipid peroxide in the sample was expressed as μmol of lipid peroxides/(kg of muscle).

Determination of TBARS

On the day of analysis, a solution of 50% trichloroacetic acid (TCA) with 1.3% thiobarbituic acid (TBA) was prepared by mixing and heating to 65°C to dissolve solutes. A 1.2 ml volume of the TCA-TBA reagent was the added to each sample (0.1 g) and the sample was mixed via inversion and heated at 65°C for 60 min (Guohua, HH-60, China). The sample was then centrifuged at 1,600 g for 5 min (Eppendorf centrifuge, 5411D, Germany). Absorbance of supernatants was read at 532 nm (Keda, UV8500, China). A standard curve was constructed using tetraethoxypropane and concentrations of TBARS in samples were expressed as μmol of TBARS/(kg of muscle).

Fatty acid analysis and calculations

A 50 g sample of ld was freeze dried for the determination of fatty acid. Fatty acid methyl ester (FAME) synthesis was conducted according to O’Fallon et al. (2007). The fatty acid composition of FAME was determined by capillary GC on a SPTM-2560, 100 m×0.25 mm×0.20 μm capillary column (Supelco, Bellefonte, PA, USA) installed on a Agilent 6890 GC (Agilent, Santa Clara, USA). The initial oven temperature was 140°C, held for 5 min, subsequently increased to 240°C at a rate of 4°C/min, and then held for 20 min. Helium was used as the carrier gas at a flow rate of 0.5 ml/min, and the column head pressure was 280 kPa. The injector and the detector were set at 250°C and 260°C, respectively. The split ratio was 30:1. Fatty acids were identified by comparing their retention times with the fatty acid methyl standards (Ample, California, USA). Saturated fatty acids (SFA) were the sum of C15:0, C16:0, C17:0, C18:0, C20:0, and C22:0. Monounsaturated fatty acids (MUFA) were the sum of C14:1n5, C16:1n7, C17:1n7, C18:1n9t, C18:1n9c, and C20:1n9. Polyunsaturated fatty acids (PUFA) were the sum of C18:2n6t, C18:2n6c, C18:3n6, C18:3n3, C20:2, C20:3n6, C20:4n6, C20:5n3, and C22:6n3. N-6 fatty acids were the sum of C18:2n6t, C18:2n6c, C18:3n6, C20:3n6, and C20:4n6. N-3 fatty acids were the sum of C18:3n3, C20:5n3, and C22:6n3.

Statistical analysis

The effect of breed on meat characteristics, muscle fiber lipid oxidation products and fatty acids were subjected to one-way analysis of variance using Generalized Linear Models procedures of SAS (2000). The significance differences between least square group means were compared using the PDIFF test of SAS (2000).


Comparison of meat quality traits

Lightness (L*), redness (a*) and chroma (C) of ld muscle were similar among all cattle breeds (Table 1), however, yellowness (b*) was significantly lower in QC than in LIM and LX cattle breeds. The Hue value was significantly lower in QC, SIM, LX and JN than in LIM. Most of the subcutaneous fat colorimetric parameters did not differ significantly among the cattle breeds, except Hue which was lower in QC than in other cattle breeds. Drip loss and Warner-Bratzler-Shear (WBS) did not differ significantly among these breeds, while cooking loss and pH (24 h) in LIM was the lowest and the highest, respectively among the tested cattle breeds.

Comparison of meat chemical composition

The proportion of dry matter was significantly lower in LIM than in other cattle breeds, while crude protein was the highest in LIM among the tested breeds (Table 2). No effect of breed on ether extract was recorded. The proportion of ash was significantly higher in JN and LX than in QC, but the mean values in LIM and SIM were intermediate to and did not differ significantly from the values of the LX and QC breeds.

Comparison of muscle fiber characteristics

The red muscle fiber (R) percentage of the ld was significantly higher in LX and LIM breeds than in other breeds (Table 3). Intermediate muscle fiber (I) percentage was significantly higher in QC than in JN, with the LIM, SIM and LX breeds taking the intermediate positions. White muscle fiber (W) percentage was significantly lower in LX and LIM breeds than in other cattle breeds. The diameters of R, I and W muscle fibers were significantly larger in QC than in other cattle breeds. Red muscle fiber density was higher in LX and LIM breeds than in other breeds, whereas white muscle fiber in LX and LIM was lower than in other breeds. Intermediate muscle fiber density was lower in LX than in SIM, but the mean values in LIM, QC and JN were intermediate to and did not differ significantly from the values of the LX and SIM breeds.

Comparison of lipid oxidation

The lipid hydroperoxides were increased with the storage time at 4°C of air exposure for all the cattle breeds (Figure 1). A significant difference of lipid hydroperoxides among cattle breeds was observed. Lipid hydroperoxides were significantly higher in QC compared with LIM, with the SIM, LX and JN taking the intermediate values from 0 to 8hours. From 12 to 72 h, lipid hydroperoxides were lower in LIM than in QC and LX, with the SIM and JN taking the intermediate values.
Similar trends were obtained for TBARS (Figure 2). The TBARS were also increased with the storage time at 4°C for all the cattle breeds. The values of TBARS were significantly lower in LIM and LX than in QC from 0 to 8 hours. From 12 to 72 h, TABRS were significantly lower in LIM than in QC, with the LX, SIM and JN breeds having the intermediate positions.

Comparison of fatty acids

Values of fatty acids in the major fatty acid classes of these cattle breeds are presented in Table 4. The total fatty acids, saturated fatty acid (SFA), and MUFA did not differ significantly among the five cattle breeds. Compared to other four breeds, QC had higher PUFA, n-6 fatty acids and n-3 fatty acids. The value of n-6:n-3 ratio was significantly lower in QC and LIM than in JN, but the mean values in SIM and LX were intermediate to and did not differ significantly from the values of the QC, LIM and JN breeds.


Meat quality traits

Meat color is a further important determinant of visual appearance of meat (Chambaza et al., 2003) and can influence the purchasing decisions of the consumers (Mancini and Hunt, 2005). Brewer et al. (2001) reported that L* value was most correlated to visual color, and using L* in conjunction with a* explained 69% of the variability in the visual pink color. Pigment content and oxidation state accounted for much of the variation in a* values (Mancini and Hunt, 2005; Waritthitham et al., 2010), while redox state and intramuscular fat content influenced b* value (Mancini and Hunt, 2005; Bispo et al., 2010; Waritthitham et al., 2010). Hue was negatively correlated to redness (Insausti et al., 1999). In term of muscle color, the five cattle breeds didn’t differ in our study in the degree of lightness (L*) and redness (a*) and all of the values were in agreement with Chambaza et al. (2003), Vieira et al. (2007) and Muchenje et al. (2008). In the present study, most of the fat color parameters didn’t differ among the cattle breeds. The values for L* in subcutaneous fat were higher and for b* were lower than those reported by Vieira et al. (2007). All the cattle breeds had fine muscle and fat colors, especially, LIM and LX had better muscle color in the current study.
With an exception of LIM, the pH (24 h) values of the other four cattle breeds were within the normal range and similar to the previous reports (Vieira et al., 2007; Muchenje et al., 2008; Bispo et al., 2010). Waritthitham et al. (2010) and Bispo et al. (2010) reported that pre-slaughter stress which leads to glycogen depletion may influence the ultimate muscle pH. However, all the cattle in this study were kept in the same environment at the abattoir over night, so it may be not the pre-slaughter stress factor that led to the higher pH values 24 h of LIM meat. The pH decline of meat was influenced by the rate of muscle cooled (Hwang and Thompson, 2001) and the muscle temperature decline was affected by carcass weight during chilling (Pike et al., 1993). So the higher pH values at 24 h in LIM may be ascribed to their heavier carcass weights.
According to Hur et al. (2009), high pH was closely related to high water-holding capacity. LIM cattle had better water-holding capacity than that of other cattle breeds in the present study, this may be due to their higher pH values. However, Hwang et al. (2010) reported that there were no significant differences in drip loss among three parts of muscle, although ld muscle had a higher pH (24 h) compared to the other muscles. Thus a further mechanism study is needed to clarify the relationship between pH and water holding capacity.

Meat chemical composition

Except for ether extract, there was a breed effect on meat chemical composition in the present study, which agrees with Muchenje et al. (2008) and Strydom et al. (2001). The chemical composition results were similar to the reports by Muchenje et al. (2008) and Waritthitham et al. (2010). However, the dry matter content was lower than that reported by Vieira et al. (2007) in which all the adults steers’ dry matter composition were higher than 27% at 42 months old, so the difference may be due to their different slaughter age or hormone effect.

Muscle fiber characteristics

Waritthitham et al. (2010) and Hoving-Bolink et al. (1999) reported that breed influenced the meat tenderness by affecting collagen content and myofibrillar structure of muscle. However, some other studies carried out by Muchenje et al. (2008), Vieira et al. (2007) and Chambaza et al. (2003) showed that no differences in the tenderness of the meat among cattle breeds were detected. In the present study, the Warner-Bratzler-Shear (WBS) values were similar among all the cattle breeds and between 3.5 kg and 6 kg. According to Bruce, Stark, and Belilken (2004), all the meat could be classified as of average toughness.
It has been indicated that the red muscle has a higher content of oxidative enzymes and mitochondria than does white muscle (Dubowitz and Everson Pearse, 1960; Lee et al., 2010). Gauthier (1969) demonstrated that the red portion of the muscle was composed predominantly of red (52%) and intermediate (40%) fibers. The results in the present study showed a similar trend, in which LIM and LX had relative better muscle color with higher percentage of red and intermediate muscle fibers. Strydom et al. (2000) reported that there were significant positive within-breed relationships between muscle tenderness and intermediate fiber percentage. Increasing the proportion of slow-twitch type I fibers percentage and area had been reported to improve tenderness in cattle (Maltin et al., 1998; Strydom et al., 2000; Hwang et al., 2010). In this study, though LX and LIM breeds had a higher percentage and density of red and intermediate fibers there were no significant differences in WBS values compared to that of the other cattle breeds, although the two cattle breeds had relative lower WBS values.

Lipid oxidation and fatty acids

Lipid oxidation was a leading cause of quality deterioration in meat and meat products (Hur et al., 2009). As Warren et al. (2008) reported, this study also found that breed had an effect on lipid oxidation. The PV and TBARS in LIM were significantly lower than in QC, which indicated that LIM cattle had better antioxidant ability. Berruga et al. (2005) suggested that lipid oxidation promoted oxymyoglobin oxidation and was significantly negatively correlated with redness. In this study, QC cattle also showed a relative lower redness, which agrees with the previous study. Skeletal muscle was susceptible to oxidative deterioration due to a combination of lipid oxidation catalysts and membrane lipid systems that were high in unsaturated fatty acids (Chan and Decker, 1994). Breed has an effect on fatty acids composition in muscle (Holló et al., 2001; Dance et al., 2009; Juárez et al., 2009). In this study, QC had the highest PUFA values among the five breeds, which should lead to lipid oxidation occurring more easily in this breed than in other breeds. However, an increase in PUFA and lower n-6:n-3 ratios are desirable for human health. If some antioxidative materials such as α-tocopherol and β-carotene were added in the diet, the lipid oxidation characteristics of QC meat might be improved.


In this study, no effect of breed on WBS, crude extract and most of the muscle and fat color parameters was recorded. However, LX and LIM showed better muscle fiber characteristics and LIM cattle also had better water holding capacity and antioxidant ability, so all these traits in the two cattle breeds are advantages for extending meat shelf life. QC had the lowest antioxidant ability among the five cattle breeds, which should be due to the higher composition of polyunsaturated fatty acids in this breed.


This research is financed by China National Supporting Project (No. 2006BAD12B02) and the Earmarked Fund for Modern Agro-Industry Technology Research System (Beef Cattle and Yaks, CARS-38).

Figure 1
Comparison of lipid hydroperoxides at different times in the longissimus dorsi (ld) muscle of five cattle breeds (μmol/kg) (N = 8). Data are presented as mean±SD. Values with different superscript letters are significantly different (p<0.05).
Figure 2
Comparison of TBARS at different times in the longissimus dorsi (ld) muscle of five cattle breeds (μmol/kg) (N = 8). Data are presented as mean±SD. Values with different superscript letters are significantly different (p<0.05).
Table 1
Comparison of meat traits of the five cattle breeds
Item Breed1 SEM p

Meat color (24 h)
 L* 38.92 35.80 38.45 36.32 36.95 1.065 0.195
 a* 19.81 19.52 20.52 18.64 20.57 0.927 0.336
 b* 9.96a 9.11ab 9.59a 7.92b 9.43ab 0.633 0.092
 C 21.13 21.55 22.67 20.27 22.63 1.092 0.268
 Hue 28.06a 24.95b 24.90b 22.67c 24.57bc 0.816 0.0005
Subcutaneous fat color (24 h)
 L* 78.37 79.02 78.64 79.87 79.57 1.082 0.852
 a* 3.39 3.43 2.47 3.42 2.31 0.394 0.109
 b* 7.34 6.89 6.24 6.04 6.15 0.422 0.156
 C 8.18 7.75 6.83 7.06 6.63 0.491 0.157
 Hue 64.32ab 63.67ab 68.73ab 61.90b 69.75a 2.343 0.102
pH (24 h) 6.18a 5.61b 5.61b 5.73b 5.62b 0.064 0.0001
Drip loss (24 h, %) 9.57 10.29 10.26 10.32 10.08 0.424 0.7012
Cooking loss (%) 26.99b 29.38ab 31.01a 30.53a 29.04ab 1.026 0.0759
Warner-Bratzler-Shear (WBS, kg) 4.67 5.36 4.39 5.29 5.15 0.416 0.4077

Means in the same row with different superscripts are significantly different (p<0.05).

1 LIM = Limousin; SIM = Simmtental; LX = Luxi; QC = Qinchuan; JN = Jinnan.

Table 2
Comparison of chemical composition of the cattle breeds
Item Breed1 SEM p

Dry matter (%) 24.18b 25.40a 25.49a 25.34a 25.59a 0.290 0.0051
Crude protein (% DM) 88.73a 85.53ab 84.17b 87.19ab 84.48b 1.232 0.0422
Ether extract (% DM) 8.26 10.21 10.91 10.44 10.32 1.194 0.5754
Ash (% DM) 3.69bc 4.05abc 4.90ab 3.15c 5.11a 0.493 0.0261

Means in the same row with different superscripts are significantly different (p<0.05).

1 LIM = Limousin; SIM = Simmtental; LX = Luxi; QC = Qinchuan; JN = Jinnan.

Table 3
Comparison of histological characteristics of muscle fiber of the five cattle breeds
Item Breed1 SEM p

Myofiber type percentage R 29.46a 15.24b 32.73a 16.91b 20.62b 2.691 0.0001
I 26.54abc 28.58ab 24.02bc 29.17a 23.23c 1.842 0.0313
W 44.00b 56.16 a 43.24b 53.90a 56.14a 2.899 0.0001
Myofiber diameter R 35.99 b 36.55 b 38.98b 60.00a 37.58b 2.915 0.0001
I 41.49 b 39.22 b 41.42b 61.10a 42.19b 2.491 0.0001
W 49.47 c 49.46 c 59.27 b 67.80a 47.94c 2.808 0.0001
Myofiber density R 58.33ab 32.41 d 67.59 a 36.36cd 49.54 bc 6.808 0.0001
I 55.56 ab 62.04 a 48.15 b 54.04ab 51.85 ab 4.582 0.1427
W 97.22 b 121.30 a 87.96 b 98.99 b 125.00 a 8.822 0.0001

Means in the same row with different superscripts are significantly different (p<0.05).

1 LIM = Limousin; SIM = Simmtental; LX = Luxi; QC = Qinchuan; JN = Jinnan.

Table 4
Comparison of fatty acids (mg/g)1 of five cattle breeds
Fatty acid Structure Breed2 SEM p

Lauric C12:0 0.05 0.03 0.03 0.03 0.02 0.011 0.5627
Myristic C14:0 2.63 2.42 2.08 1.70 1.93 0.393 0.4336
Myristoleic C14:1n5 0.55 0.49 0.41 0.27 0.34 0.100 0.2781
Pentadecanoic C15:0 0.26 0.28 0.24 0.26 0.24 0.036 0.9271
Palmitic C16:0 21.49 22.07 19.26 18.16 19.40 2.909 0.845
Palmitoleic C16:1n7 2.91 2.36 2.20 2.03 2.26 0.440 0.6383
Heptadecanoic C17:0 0.64 0.65 0.62 0.59 0.61 0.078 0.9876
Cis-10-Heptadecenoic C17:1n7 0.47 0.41 0.41 0.35 0.40 0.059 0.7008
Stearic C18:0 13.32 14.05 14.02 14.85 13.90 1.706 0.9787
Elaidic C18:1n9t 1.65 1.77 1.63 1.67 1.49 0.217 0.9267
Oleic C18:1n9c 27.73 30.86 25.66 22.68 26.12 3.876 0.6354
Linolelaidic C18:2n6t 0.18 0.19 0.16 0.15 0.15 0.028 0.7552
Linoleic C18:2n6c 3.63b 3.67b 4.08b 4.77a 3.86b 0.227 0.0059
Arachidic C20:0 0.09a 0.09a 0.10a 0.03b 0.10a 0.013 0.0011
γ-Linolenic C18:3n6 0.07ab 0.10a 0.08ab 0.03b 0.10a 0.022 0.0527
Eicosenoic C20:1n9 0.13a 0.13a 0.12ab 0.08b 0.12ab 0.015 0.0406
Linolenic C18:3n3 0.13ab 0.12ab 0.13ab 0.16a 0.09b 0.020 0.0693
Eicosadienoic C20:2 0.16ab 0.22a 0.10b 0.08b 0.11b 0.036 0.0462
Behenic C22:0 0.08 0.09 0.12 0.05 0.1 0.032 0.5387
Eicosatrienoic C20:3n6 0.03b 0.03b 0.05b 0.26a 0.06b 0.004 0.0004
Arachidonic C20:4n6 0.45b 0.46b 0.62b 1.01a 0.58b 0.084 0.0002
Eicosapentaenoic C20:5n3 0.11 0.1 0.08 0.1 0.09 0.044 0.9815
Docosahexaenoic C22:6n3 0.26ab 0.2b 0.14b 0.61a 0.18b 0.014 0.1339
SFA3 38.56 39.69 36.47 35.68 35.27 4.586 0.9506
MUFA4 33.44 36.02 30.44 26.78 29.65 4.183 0.5808
PUFA5 5.01b 5.05b 5.41b 6.96a 5.06b 0.320 0.0004
n-66 4.35b 4.43b 4.98b 6.19a 4.65b 0.286 0.0004
n-37 0.5ab 0.39b 0.33b 0.8a 0.31b 0.112 0.0230
n-6:n-3 12.31b 18.14ab 18.7ab 8.93b 22.99a 3.369 0.0339
Total 77.00 80.75 72.31 69.42 69.98 8.884 0.8363

1 Milligrams per gram of freeze-dried tissue.

2 LIM = Limousin; SIM = Simmtental; LX = Luxi; QC = Qinchuan; JN = Jinnan.

3 SFA = C12:0+C14:0+C15:0+C16:0+C17:0+C18:0+C20:0+C22:0.

4 MUFA = C14:1n5+C16:1n7+C17:1n7+C18:1n9t+C18:1n9c+C20:1n9.

5 PUFA = C18:2n6t+C18:2n6c+C18:3n6+C18:3n3+C20:2+C20:3n6+C20:4n6+C20:5n3+C22:6n3.

6 n-6 = C18:2n6t+C18:2n6c+C18:3n6+C20:3n6+C20:4n6.

7 n-3 = C18:3n3+C20:5n3+C22:6n3.


AOAC. 1985. Official methods of analysis. 16th edWashington, DC: Association of Official Analytical Chemists.

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