For centuries, the humid West African coastal country of Benin attracts cattle herders from neighboring Sahelian countries such as Niger, Burkina Faso and Nigeria. Each year, several thousands of cattle are trekked over hundreds of kilometers to Benin following established and non-established transhumance corridors. This cross-border mobility has been shown to play an important role in ensuring the productivity of the transhumant herds through adequate late dry season access to pastoral resources. Yet, its effects on the traditional agro-pastoral production systems that are encountered along the routes in Benin have never been explicitly investigated. Therefore, we collected socio-economic household data, herd characteristics and management data from 104 resident herders and 38 transhumant herders in 2 vegetation zones of Benin. To determine whether or not the proximity to transhumance corridors affects sedentary production systems, characteristics of cattle herds and farmers’ management practices were compared between villages close to (within a 25 km buffer) and far from (outside a 25 km buffer) transhumance corridors within and between vegetation zones using non-parametric statistical tests. Existing relationships between resident and transhumant herders were also identified and characterized. Subsequently, herd characteristics and management practices were compared between resident herders having relationships with transhumant herders and those without. Herd sizes of resident herders living close to transhumance corridors were larger (P < 0.01) than those of their counterparts living far away. Also, proximity to transhumance corridors had positive effects on herd management practices. The relationships between resident and transhumant herders were governed by a variety of interests including encampment/manuring contracts, exploitation of grazing lands and watering points, trading and bartering of cattle. This exchange of cattle is an important driver of change in the breed composition of local herds and represents an opportunity for resident herders to enhance their herds’ productivity through crossbreeding. However, the mere replacement or indiscriminate crossbreeding of local cattle breeds with those kept by transhumant herders threatens the sustainability of the traditional resident herding systems by increasing the risk of genetic erosion and loss of valuable adaptive traits in indigenous animal genetic resources.

In addition to the main components of the somatotrophic axis (GH/GHR/IGF-I/IGF-IR), great importance in the control of growth and development is also attached to the Janus kinase 2 (JAK2) pathway. Induced by the GH/GHR complex, JAK2 activates signal transducer and activator of transcription 5 (STAT5), and in consequence, may be involved in the regulation of expression of insulin-like growth factor I (IGF-I) in the mammary gland. Silent mutation (rs110298451) has been identified within exon 20 using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP). A total of 904 individuals of four dairy or dual-purpose breeds (Polish Holstein-Friesian, Montbeliarde, Simmental and Jersey) were genotyped. A genotypic imbalance in the populations was observed. In the case of dual-purpose breeds (Montbeliarde and Simmental), the frequencies of both alleles were almost equal. In contrary, the JAK2G allele was predominant in the Polish Holstein-Friesian breed while JAK2A allele in Jersey. A pronounced relationship between JAK2/RsaI polymorphism and milk production traits was found where, irrespective of breed and lactation order, the GG genotype was significantly associated with higher milk, protein and fat yields, as compared to the AA genotype. Heterozygous individuals were generally characterised by intermediate values of the analysed milk traits. It can be argued that the JAK2 gene polymorphism is a potential marker for milk production traits. However, due to the fact that rs110298451 SNP does not directly affect amino acid sequence, other association studies involving missense mutation should also be performed.

The aim of this study was to investigate the accuracy to predict detailed fatty acid (FA) composition of bovine milk by mid-infrared spectrometry, for a cattle population that partly differed in terms of country, breed and methodology used to measure actual FA composition compared with the calibration data set. Calibration equations for predicting FA composition using mid-infrared spectrometry were developed in the European project RobustMilk and based on 1236 milk samples from multiple cattle breeds from Ireland, Scotland and the Walloon Region of Belgium. The validation data set contained 190 milk samples from cows in the Netherlands across four breeds: Dutch Friesian, Meuse-Rhine-Yssel, Groningen White Headed (GWH) and Jersey (JER). The FA measurements were performed using gas–liquid partition chromatography (GC) as the gold standard. Some FAs and groups of FAs were not considered because of differences in definition, as the capillary column of the GC was not the same as used to develop the calibration equations. Differences in performance of the calibration equations between breeds were mainly found by evaluating the standard error of validation and the average prediction error. In general, for the GWH breed the smallest differences were found between predicted and reference GC values and least variation in prediction errors, whereas for JER the largest differences were found between predicted and reference GC values and most variation in prediction errors. For the individual FAs 4:0, 6:0, 8:0, 10:0, 12:0, 14:0 and 16:0 and the groups’ saturated FAs, short-chain FAs and medium-chain FAs, predictions assessed for all breeds together were highly accurate (validation R2 > 0.80) with limited bias. For the individual FAs cis-14:1, cis-16:1 and 18:0, the calibration equations were moderately accurate (R2 in the range of 0.60 to 0.80) and for the individual FA 17:0 predictions were less accurate (R2 < 0.60) with considerable bias. FA concentrations in the validation data set of our study were generally higher than those in the calibration data. This difference in the range of FA concentrations, mainly due to breed differences in our study, can cause lower accuracy. In conclusion, the RobustMilk calibration equations can be used to predict most FAs in milk from the four breeds in the Netherlands with only a minor loss of accuracy.

In previous studies, significant differences in Mycobacterium bovis infection prevalence was reported between two Chadian cattle breeds. Those findings and the established differentiation due to phenotypic characteristics suggest that the two breeds (Arab and Mbororo) are genetically different. To evaluate the genetic structure and the differences between these breeds, the genetic diversity within and between breeds was evaluated based on a total of 205 multilocus genotypes (21 microsatellite loci).

All of the loci under investigation were polymorphic and the number of alleles ranged from 4 to14 within the two populations. The analysis of population fixation resulted in a FST value of 0.006. Further the population assignment of the individual genotypes and the exact test of population differentiation did not support the hypothesis that the samples drawn from the two populations are genetically different. Population admixture and sample collection are discussed as possible reasons for the rejection of the hypothesis. Finally, recommendations for sample collection in extensive systems are given.

As a result of multiple QTL-mapping projects in recent years, a quantitative trait locus for milk fat percentage and milk yield has been described on BTA14. Recent reports name the acyl-CoA[ratio ]diacylglycerol acyltransferase (DGAT1) gene on BTA14 as a potential candidate gene, with a nonconservative substitution of lysine by alanine (K232A) producing a major effect on milk composition and yield. DGAT1K appears to be the ancestral allele and the K232A substitution probably occurred after the divergence of the Bos indicus and Bos taurus lineages. These findings prompted us to genotype 1748 DNA samples of 38 different Bos taurus and Bos indicus cattle breeds from 13 countries on five continents (Europe, Africa, Asia, North America and South America), to examine the occurrence of the DGAT1 polymorphism and characterize the K232A substitution in cattle breeds of different origins and selected for different purposes (e.g., beef, dairy and dual purpose). Calculating pairwise FST values for pooled subpopulations showed least divergence for Bos indicus breeds with high milk fat percentage. Fixation of DGAT1A was found in some Bos taurus breeds and fixation of DGAT1K in one Bos indicus breed. Breeds of no known organized breeding background from the Near East domestication centre of Bos taurus and taurine African N'Dama cattle were found to possess intermediate frequencies of DGAT1K. While beef breeds tended to harbour higher DGAT1A levels, dairy cattle showed everything from very low levels of DGAT1K to unexpectedly high frequencies of this allele.

Japanese Black cattle (Wagyu), deposit much higher amounts of intramuscular fat, known as marbling, than other breeds of cattle. To determine whether this unique fat deposition is attributable to the somatotropic axis, we compared pulsatile growth hormone (GH) secretion, plasma levels of insulin-like growth factor-1 (IGF-1) and cellular density of somatotrophs (GH-expressing cells) in the anterior pituitary glands of Japanese Black and Holstein steers. Blood samples were withdrawn every 15 min for 6 h from 14 Japanese Black and 12 Holstein steers at about 17 months of age, and GH and IGF-1 concentrations were determined. The distribution and proportion of GH-expressing cells were analysed by immunohistochemistry combined with point-count morphometry in pituitaries from six steers from each breed aged about 18 to 21 months. Overall mean and baseline plasma GH concentrations were lower (P < 0·001) in Japanese Black than Holstein steers. In addition, Japanese Black had smaller (P < 0·05) amplitudes of GH secretory pulses than Holstein steers, whereas the GH pulse frequency did not differ between the breeds. Japanese Black steers also had lower (P < 0·001) plasma levels of IGF-1 than Holstein steers. The marbling score of Japanese Black steers was higher (P < 0·001) than that of Holsteins at the same carcass weight. The proportion of GH-expressing cells was smaller (P < 0·05) in Japanese Black than Holstein steers at the hind dorsal and hind ventral regions of the adenohypophysis. Thus, in Japanese Black and Holstein steers, the breed difference in the relative density of GH-expressing cells corresponded to that in profiles of pulsatile GH secretion. These results suggest that the features of the somatotropic axis intrinsically differ between Japanese Black and Holstein cattle and that these features may be partly responsible for the genetic ability of the former to deposit greater amounts of marbling fat and for the smaller frame of Wagyu cattle.

Carcass traits of two indigenous African (Sanga) breeds (Afrikaner and Nguni), one indigenous African composite breed (Bonsmara), one foreign composite breed (Santa Gertrudis) and two continental European breeds (Brown Swiss and Pinzgauer) were compared. Treatment means were adjusted to the mean overall subcutaneous fat proportion (47 g/kg). Despite differences in maturity type, only the Afrikaner dressed out significantly (P < 0·05) lower than the foreign breeds. Both Sanga breeds and the Bonsmara had significantly higher muscle yields than the Santa Gertrudis and Pinzgauer, mainly due to the high intermuscular fat of the latter two breeds. When muscle yield was expressed per unit of bone, the Afrikaner and Bonsmara compared favourably with the larger breeds, due to their low bone and intermuscular fat yield, while the Nguni had a relatively high bone yield. The Santa Gertrudis had the lowest muscle yield due to its high bone and intermuscular fat yields, especially when compared with the smaller Bonsmara composite. Both Sanga breeds had significantly higher (P < 0·05) proportions of total weight, meat and bone (Afrikaner P > 0·05) in the high-priced cuts compared with the other breeds at the same subcutaneous fat level. Despite the statistical significance, differences were small in magnitude and probably of little commercial value. At the same time mean subcutaneous fat proportion, tissue yield and distribution patterns expected of late maturing breeds were observed for smaller indigenous breeds, suggesting that it was specific breed effects rather than maturity type effects, which were evident.

One hundred and twenty spring-born steers, comprising 40 Friesians (FR), 40 Meuse-Rhine-lssel (MRI) × Friesians (MR), and 40 Belgian Blue × Friesians (BB) were reared together from 3 weeks of age to the start of their second winter. During the second winter there was a 3 (FR, MR and BB breed types) × 2 (3 kg and 6 kg supplementary concentrates per head daily with grass silage ad libitum) × 2 (96- and 220-day finishing periods) factorial arrangement of treatments (10 animals per subgroup). Carcass weights and grades were recorded after slaughter at the end of the second winter, and one side from each of 96 carcasses (eight per subgroup) was dissected into bone, muscle, intermuscular fat and subcutaneous fat. A sample of m. longissimus from the 10th rib was chemically analysed. Slaughter weights and carcass weights per day from arrival to slaughter were 796, 813 and 828 (s.e.d. 11·7) g and 419, 440 and 457 (s.e.d. 7·1) g for FR, MR and BB, respectively. Corresponding carcass weights were 314, 329 and 342 (s.e.d. 4·5) kg. BB had better conformation than both FR and MR. BB also had a lower carcass fat score, lower proportions of bone, intermuscular fat and subcutaneous fat, a higher proportion of muscle and muscle with higher proportion of moisture and a lower proportion of lipid than FR and MR. The higher level of concentrates increased side iveight by 8 kg, but the overall effects on carcass composition were small. The longer finishing period increased side weight by 25 kg and was associated with significantly reduced proportions of bone and muscle and an increased proportion of fat. Allometric regression coefficients for carcass weight on slaughter weight, and for bone, muscle and fat weights on side weight were 1·19, 0·39, 0·80 and 2·16, respectively. It is concluded that despite the better carcass conformation of MR, there was little difference in carcass and muscle composition between FR and MR. BB, in addition to having a higher growth rate and better carcass conformation than FR, also had more muscle in the carcass, more of the total muscle in the higher value joints and a lower proportion of lipid in the muscle. It was calculated that FR, MR and BB would have similar proportions of separable fat in the carcass at approximate carcass weights of 300, 320 and 400 kg, respectively.

Body composition was studied in 20 mature, non-pregnant, non-lactating cows from five breeds (Hereford, Aberdeen Angus, Dexter, British Friesian and Jersey) kept on four feeding levels until they attained equilibrium body weights that were proportionately 0·7,0·9,1·1 or 1·3 of their normal adult body weight.

Significant breed differences were found in the proportions of body tissues and organs and these were associated with breed differences in lactability (i.e. genetic milking potential adjusted for body size). As a proportion of body weight, intra-abdominal fat, liver, spleen and uterus increased significantly with lactability and hide decreased significantly. Empty gut and gut fill also increased with lactability but not significantly. Liver proportion in dairy breeds was 1·26 times the proportion in beef breeds. Corresponding values for intra-abdominal fat and hide were 1·43 and 0·83.

The most dramatic increases with feeding level were in the proportions of subcutaneous fat, both intra-abdominal fat depots, and the udder. All fat depots were completely depleted when body weight decreased to about 0·6 of its normal adult value. Strong decreases occurred in the proportion of muscle, carcass bone and offal. The proportion of empty gut decreased significantly with increased feeding level. Liver, tail, thymus and possibly gut fill were the only traits entirely unaffected by feeding level.

The near-constancy of liver proportion at equilibrium implies that the rapid response of the liver to a change in feeding level is eventually matched in magnitude by the slower responses in other tissues and organs, so that the original proportionality of about 1 kg body tissue for each 10 g liver is eventually restored.

The chemical composition of the muscle and fatty carcass tissues of Hereford × Friesian (HE), Friesian (FR) and Charolais × Friesian (CH) steers finished on high (H) (12·6 MJ/kg dry matter) and medium (M) (10·4 MJ/kg dry matter) metabolizable energy (ME) concentration diets and slaughtered at low (L), normal (N) and heavy (W) carcass weights was determined in a 3 × 2 × 3 (no. = 9) factorial experiment. There were also pre-finishing slaughter groups of nine animals of each breed type. Target L, N and W carcass weights were 260, 300 and 340 kg, for HE and FR and 260, 320 and 380 kg, for CH, respectively.

Main effect side soft tissue weights of the finished groups were 128, 125 and 134 (s.e.d. 1·3) kg for HE, FR and CH, 133 and 125 (s.e.d. 1·1) kg for H and M and 108, 129 and 150 (s.e.d. 1·3) kg for L, N and W, respectively. Soft tissue chemical composition was 540, 562 and 590 (s.e.d. 5·0) g/kg moisture, 162, 174 and 181 (s.e.d. 1·7) g/kg protein and 288, 254 and 220 (s.e.d. 6·6) g/kg lipid for HE, FR and CH and 558 and 570 (s.e.d. 4·1) g/kg moisture, 170 and 175 (s.e.d. 1·4) g/kg protein and 262 and 246 (s.e.d. 5·4) g/kg lipid for H and M, respectively. The allometric regression coefficients for moisture, protein and lipid weights on soft tissue weight were 0·65, 0·69 and 206, respectively. The coefficients for moisture and protein weights on muscle and fat weights were < 1·0, whereas for lipid, they were >1·0. The breed differences in soft tissue chemical composition paralleled differences in physical composition. Dietary ME concentration had little effect on the chemical composition of individual tissues. For the M diet, HE, FR and CH were calculated to have similar soft tissue lipid concentrations (250 g/kg) at side soft tissue weights of 113, 125 and 157 kg, respectively. Corresponding side muscle weights at similar muscle lipid concentration (70 g/kg) would be 77, 90 and 108 kg.

The carcass composition of Hereford × Friesian (HE), Friesian (FR) and Charolais × Friesian (CH) steers finished on diets of high (H) and medium (M) dietary metabolizable energy (ME) concentrations and slaughtered at low (L), normal (N) and heavy (W) carcass weights was examined in a 3 × 2 × 3 (no. = 9 per individual treatment) factorial experiment. A pre-finishing slaughter group of nine animals of each breed type was also included, giving a total 189 animals in 21 experimental groups. ME concentrations of the H and M diets which were offered ad libitum were 12·6 and 10·4 MJ/kg dry matter. Target carcass weights for L, N and W were 260, 300 and 340 kg for HE and FR and 260, 320 and 380 kg for CH.

Carcass side weights (before tissue separation) of the HE, FR and CH pre-finishing slaughter groups were 90·8, 970 and 101·0 (s.e.d. 3·9) kg. Corresponding tissue proportions were 188, 199 and 200 (s.e.d. 4·3) g/kg bone, 663, 686 and 690 (s.e.d. 5·3) g/kg muscle and 135, 99 and 96 (s.e.d. 5·7) g/kg fat. Main effect side weights of the finished groups were 152·3, 151·4 and 162·2 (s.e.d. 1·4) kg for HE, FR and CH. 158·5 and 152·2 (s.e.d. 1·1) kg for H and M and 131·2, 155·2 and 179·6 (s.e.d. 1·4) kg for L, N and W, respectively. Tissue proportions in the same order were 146, 160 and 157 (s.e.d. 2·0), 149 and 159 (s.e.d. 1·6) and 163, 154 and 146 (s.e.d. 2·0) g/kg bone, 579, 601 and 635 (s.e.d. 5·5), 600 and 610 (s.e.d. 4·5) and 637, 599 and 574 (s.e.d. 5·5) g/kg muscle and 264, 228 and 195 (s.e.d. 6·4), 240 and 219 (s.e.d. 5·2) and 188, 235 and 264 (s.e.d. 6·4) g/kg fat. CH had more (P < 0·001) of their muscle in the pelvic limb and less (P < 0001) in the thorax than HE and FR. HE had more (P < 0·001) of their carcass fat in the subcutaneous depot and less (P < 0·001) in the intermuscular depot than FR and CH. The allometric regression coefficients for the main joint and tissue weights on side weight were <1·0 for both limbs, loin, bone and muscle. Coefficients were >1·0 for the thorax, ribs, flank and fat. The regression coefficients for the main muscles of the pelvic limb and loin and total thoracic limb muscle on total side muscle were <l·0, while the coefficients for the flank, ribs and thorax muscles were >1·0. Similarly the regression coefficients for the bones of the two limbs on total side bone were <10, while the coefficients for the loin, ribs and thorax bones were >10. It was calculated (for the H diet) that at a carcass weight of 300 kg, HE, FR and CH would have carcass tissue proportions of 576, 600 and 642 g/kg muscle and 261, 227 and 180 g/kg fat. The three breed types would have similar carcass fat contents at carcass weights of 264, 300 and 376 kg for HE, FR and CH, respectively.

One hundred and sixty-two spring born steers comprising 54 Charolais × Friesian (CH), 54 Hereford × Friesian (HE) and 54 Friesians (FR) were reared together from shortly after birth until the end of their second grazing season at a mean age of 573 days. The animals were then blocked on weight within genotype, housed in a slatted shed and allocated to either a high (12·6 MJ metabolizable energy (ME) per kg) or a medium (10·4 MJ ME per kg) energy diet offered ad libitum until slaughter at one of three target carcass weights · light (260 kg (HE, FR and CH)), normal (300 kg (HE and FR) and 320 kg (CH)) or heavy (340 kg (HE and FR) and 380 kg (CH)) to give a 3 (breed type) · 2 (energy level) · 3 (slaughter weight) factorial arrangement during the finishing winter. The trial was repeated in 3 years consecutively.

CH were significantly heavier than HE at all times up to 18 months of age when they were 43 kg heavier, at which stage they were also 24 kg heavier than FR. CH grew significantly faster at pasture than HE in both seasons and faster than FR in the second season. HE had the best daily gain in the finishing period.

Overall slaughter weights per day of age, carcass weights per day of age and carcass weights of CH, HE and FR were 812, 771 and 761 (s.e. 9·2) g, 448, 418 and 405 (s.e. 4·8) g and 318. 299 and 298 (s.e. 2·2) kg, respectively. CH had significantly better killing-out proportions (lOg/kg) than HE which in turn were 10 g/kg better than FR. CH and FR had similar carcass length, carcass depth, leg length and leg widths and both were significantly larger than HE. CH had significantly larger longissimus dorsi areas than either HE or FR (80·9 v. 67·0 and 66·4 cm-); they also had significantly better conformation scores than HE which in turn were significantly better than FR.

Increasing the energy level during the finishing period increased daily gain by proportionately 0·52 (1089 v. 684 g/day), reduced slaughter age by 51 days (711 v. 762 days) and significantly increased killing-out proportion (551 v. 534 g/kg) and conformation score (4·86 v. 4·64). Offal as a proportion of empty live weight tended to be higher for FR than for HE or CH, the exception being the hide, which was significantly lower for FR.