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Cow-calf and feedlot performances of Brahman-derivative breeds.

A study was conducted to compare Brangus, Beefmaster, Gelbray, and Simbrah breed influences for economically important traits. Brangus (9), Beefmaster (12), Gelbray (10), and Simbrah (7) sires were used in purebred and crossbred (Brahman x Hereford F1 cows) matings to generate calves (326) in eight breed groups. Beefmaster cows were of similar size (448 kg), Brangus and Gelbray cows were 11% heavier (501 and 503 kg), and Simbrah cows were 21% heavier (548 kg) compared to Brahman x Hereford F1 cows (452 kg). Calves sired by Brangus and Beefmaster bulls had lower birth weights (35 vs 38 kg; P < 0.05), preweaning growth rates (0.87 vs 0.91 kg x d(-1); P < 0.01), and weaning weights (206 vs 219 kg; P < 0.01) than Gelbray- and Simbrah-sired calves. Birth weights, preweaning ADG, and weaning weight and hip heights were similar between Brangus- and Beefmaster-sired calves. Simbrah-sired calves had greater preweaning growth rates (0.94 vs 0.88 kg x d(-1); P < 0.05), weaning weights (227 vs 211 kg; P < 0.01), and adjusted 205-d hip heights (126 vs 122 cm; P < 0.05) than Gelbray-sired calves. Straightbred Angus steers were introduced in the postweaning portion of the study. Steer calves were placed on feed at an average age of 14.5 mo. Steers were removed from the feedlot upon attaining a targeted 10 mm of backfat. Feedlot ADG did not differ among sire breeds. Brahman-derivative sired steers required an additional 54 d on feed (P < 0.01) and were 86 kg heavier (P < 0.01) at harvest than Angus steers. Continental-Brahman steers spent an additional 25 d on feed (P < 0.05) and were 35 kg heavier (P < 0.01) at harvest than British-Brahman steers. Simbrah-sired steers were 52 kg heavier (P < 0.01) at harvest than Gelbray-sired steers when fed for a similar number of days (211 vs 203 d). However, straightbred Simbrah steers required an additional 12 d on feed (P < 0.01) and weighed 47 kg more (P < 0.01) than Simbrah-sired crossbred steers. The economic value of the heavier calf weaning weights may be offset by the attendant larger cow size of the Continental-Brahman compared to the British-Brahman breeds. Similarly, the heavier weights of Continental-Brahman compared to British-Brahman steers, when harvested at a prescribed level of fatness may be viewed as a benefit, but the increased number of requisite days in the feedlot is a disadvantage.

Animal Feed↗

Genetic relationships and admixture among sheep breeds from Northern Spain assessed using microsatellites.

Although many research papers have studied diversity and differentiation within livestock species, genetic relationships among neighboring populations remain poorly understood. Here we apply recent methodologies to analyze the polymorphism of 14 microsatellites in 238 unrelated individuals belonging to six sheep breeds from Northern Spain to ascertain their historical relationships and the relative genetic contributions existing between populations. Individual genotypes were analyzed to assess the existence of an underlying genetic structure. Long-term and recent migration rates were estimated to identify patterns of relative genetic contribution among breeds. The complete data set showed a strong population structure derived from both different ancestral origins and some geographical patterns of recent gene flow. Two of the analyzed breeds (Black-faced Latxa and Churra) had a marked genetic background, supporting the hypothesis that, regardless of their phenotypical similarities, they have different ancestral origins. Some of the more presumably related breeds had negative long-term admixture coefficients, showing that they diverged only recently. In addition, we show how methodologies for estimation of long-term gene flow and recent patterns of migration are complementary, providing information about migration rates on different timescales.

Animals↗

Comparison of three models to estimate breeding values for percentage of loin intramuscular fat in Duroc swine.

Three selection models were evaluated to compare selection candidate rankings based on EBV and to evaluate subsequent effects of model-derived EBV on the selection differential and expected genetic response in the population. Data were collected from carcass- and ultrasound-derived estimates of loin i.m. fat percent (IMF) in a population of Duroc swine under selection to increase IMF. The models compared were Model 1, a two-trait animal model used in the selection experiment that included ultrasound IMF from all pigs scanned and carcass IMF from pigs slaughtered to estimate breeding values for both carcass (C1) and ultrasound IMF (U1); Model 2, a single-trait animal model that included ultrasound IMF values on all pigs scanned to estimate breeding values for ultrasound IMF (U2); and Model 3, a multiple-trait animal model including carcass IMF from slaughtered pigs and the first three principal components from a total of 10 image parameters averaged across four longitudinal ultrasound images to estimate breeding values for carcass IMF (C3). Rank correlations between breeding value estimates for U1 and C1, U1 and U2, and C1 and C3 were 0.95, 0.97, and 0.92, respectively. Other rank correlations were 0.86 or less. In the selection experiment, approximately the top 10% of boars and 50% of gilts were selected. Selection differentials for pigs in Generation 3 were greatest when ranking pigs based on C1, followed by U1, U2, and C3. In addition, selection differential and estimated response were evaluated when simulating selection of the top 1, 5, and 10% of sires and 50% of dams. Results of this analysis indicated the greatest selection differential was for selection based on C1. The greatest loss in selection differential was found for selection based on C3 when selecting the top 10 and 1% of boars and 50% of gilts. The loss in estimated response when selecting varying percentages of boars and the top 50% of gilts was greatest when selection was based on C3 (16.0 to 25.8%) and least for selection based on U1 (1.3 to 10.9%). Estimated genetic change from selection based on carcass IMF was greater than selection based on ultrasound IMF. Results show that selection based on a combination of ultrasonically predicted IMF and sib carcass IMF produced the greatest selection differentials and should lead to the greatest genetic change.

Adipose Tissue↗

Joint analysis of two breed cross populations in pigs to improve detection and characterization of quantitative trait loci.

The purpose of this study was to develop and implement least squares interval-mapping models for joint analysis of breed cross QTL mapping populations and to evaluate the effect of joint analysis on QTL detected for economic traits in data from two breed crosses in pigs. Data on 26 growth, carcass composition, and meat quality traits from F2 crosses between commercially relevant pig breeds were used: a Berkshire x Yorkshire cross at Iowa State University (ISU) and a Berkshire x Duroc cross at the University of Illinois (UOI). All animals were genotyped for a total of 39 (ISU) and 32 (UOI) markers on chromosomes 2, 6, 13, and 18. Marker linkage maps derived from the individual and joint data were similar with regard to order and relative position, but some differences in absolute distances existed. Maps from the joint data were used in all analyses. The individual and joint data sets were analyzed using several least squares interval-mapping models: line-cross (LC) models with Mendelian and parent-of-origin effects; halfsib models (HS); and combined models (CB) that included LC and HS effects. Lack-of-fit tests between the models were used to characterize QTL for mode of expression and to identify segregation of QTL within parental breeds. A total of 26 (8), 47 (18), and 53 (16) QTL were detected at the 5% chromosome (genome)-wise level in the ISU, UOI, and joint data for the 26 analyzed traits. Of the 53 QTL detected in the joint data, only six were detected in both populations and for many, allele effects differed between the two crosses. Despite the lack of overlap between the two populations, joint analysis resulted in an increase in significance for many QTL, including detection of ten QTL that did not reach significance in either population. Confidence intervals for position also were smaller for several QTL. In contrast, 24 QTL, most of which were detected at chromosome-wise levels in the ISU or UOI population, were not detected in the joint data. Presence of paternally expressed QTL near the IGF2 region of SSC2 was confirmed, with major effects on backfat and loin muscle area, particularly in the UOI population, as well as one or more QTL for carcass composition in the distal arm of Chromosome 6. Results of this study suggest that joint analysis using a range of QTL models increases the power of QTL mapping and QTL characterization, which helps to identify genes for subsequent marker-assisted selection.

Animals↗

Comparison of genetic gains per year for carcass traits among breeding programs in the Japanese Brown and the Japanese Black cattle.

The breeding program for beef cattle in Japan has changed dramatically over 4 decades. Visual judging was done initially, but progeny testing in test stations began in 1968. In the 1980s, the genetic evaluation program using field records, so-called on-farm progeny testing, was first adopted in Oita, Hyogo, and Kumamoto prefectures. In this study, genetic trends for carcass traits in these 3 Wagyu populations were estimated, and genetic gains per year were compared among the 3 different beef cattle breeding programs. The field carcass records used were collected between 1988 and 2003. The traits analyzed were carcass weight, LM area, rib thickness, s.c. fat thickness, and beef marbling standard number. The average breeding values of reproducing dams born the same year were used to estimate the genetic trends for the carcass traits. For comparison of the 3 breeding programs, birth years of the dams were divided into 3 periods reflecting each program. Positive genetic trends for beef marbling standard number were clearly shown in all populations. The genetic gains per year for all carcass traits were significantly enhanced by adopting the on-farm progeny testing program. These results indicate that the on-farm progeny testing program with BLUP is a very powerful approach for genetic improvement of carcass traits in Japanese Wagyu beef cattle.

Animals↗

Effects of season and breed on the feeding behavior of multiparous lactating sows in a tropical humid climate.

The effects of breed and season on performance and feeding behavior were studied during 76 lactations in multiparous Large White (LW; n = 17) and Creole (CR; n = 23) sows reared in a humid tropical climate. The experiment was conducted in Guadeloupe (French West Indies, latitude 16 degrees N, longitude 61 degrees W) between May 2002 and July 2004. Average daily ambient temperature was greater during the hot season than during the warm season (26.0 vs. 23.8 degrees C), but relative humidity was similar in both seasons (85% on average). The daily fluctuations of ambient temperature and relative humidity were similar for both seasons. At farrowing, BW was lower (187 vs. 265 kg) and backfat thickness was greater (40 vs. 22 mm) in CR than in LW sows (P < 0.01). Sows were offered feed ad libitum between the fifth and the 26th day of lactation. There was a breed x season interaction (P < 0.05) for ADFI. During the hot season the reduction of ADFI was more pronounced in LW than in CR sows (-1,100 vs. -300 g/d). Irrespective of breed and season, the daily number of meals was 9.0. The meal size and the rate of feed intake were greater in LW than in CR sows, respectively (555 g and 153 g/min vs. 390 g and 83 g/min; P < 0.01). The diurnal proportion of ADFI was greater in CR than in LW sows (0.60 vs. 0.41; P < 0.01). The reduction in ADFI in LW sows during the hot season was mainly related to a reduction in feed intake during the day rather than during the night (-1.3 vs. -0.2 kg; P < 0.01). Duration of standing was not affected by breed or season, and it averaged 120 min/day. This study confirms the negative effect of the hot season on feeding behavior of lactating sows. It also suggests a better acclimation to daily high temperatures and a greater heat tolerance in CR compared with LW sows, at least for eating behavior.

Animals↗

Research partnerships in relation to topics in animal breeding and genetics.

A total of 1,628 papers presented at the sixth and seventh World Congresses on Genetics Applied to Livestock Production were categorized into 20 topics according to research subjects. The aim was to determine, in relation to various topics in animal breeding and genetics, the forms of partnerships and the degree of attention given in different continents. North-North partnerships (defined as cooperation between and within developed countries) had a 68.80% representation of research papers presented, whereas North-South partnerships (cooperation between developed and developing countries) had the least representation with only 8.23% of papers. Asia contributed the most research papers in biochemical genetics, whereas Australia lead in research papers on breeding for fiber and fur. Europe contributed the most to the remaining topics, and Africa usually, but not always, contributed the least to most research topics. This study provided a useful indication of the current state of literature in animal breeding and genetics and will be useful to animal breeding and genetics researchers worldwide as they chart the way forward for research and development in the field of genetics applied to livestock production in different continents.

Agriculture↗

A genetic investigation of various growth models to describe growth of lambs of two contrasting breeds.

This study compared the use of various models to describe growth in lambs of 2 contrasting breeds from birth to slaughter. Live BW records (n = 7559) from 240 Texel and 231 Scottish Blackface (SBF) lambs weighed at 2-wk intervals were modeled. Biologically relevant variables were estimated for each lamb from modified versions of the logistic, Gompertz, Richards, and exponential models, and from linear regression. In both breeds, all nonlinear models fitted the data well, with an average coefficient of determination (R2) of > 0.98. The linear model had a lower average R2 than any of the nonlinear models (< 0.94). The variables used to describe the best 3 models (logistic, Gompertz, and Richards) included estimated final BW (A); maximum ADG (B); age at maximum ADG (C); position of point of inflection in relation to A (D, for Richards only). The Richards and Gompertz models provided the best fit (average R2 = 0.986 to 0.989) in both breeds. Richards estimated an extra variable, allowing increased flexibility in describing individual growth patterns, but the Akaike's information criteria value (which weighs log-likelihood by number of parameters estimated) was similar to that of the Gompertz model. Variables A, B, C, and D were moderately to highly heritable in Texel lambs (h2 = 0.33 to 0.87), and genetic correlations between variables within-model ranged from -0.80 to 0.89, suggesting some flexibility to change the shape of the growth curve when selecting for different variables. In SBF lambs, only variables from the logistic and Gompertz models had moderate heritabilities (0.17 to 0.56), but with high genetic correlations between variables within each model (< -0.88 or > 0.92). Selection on growth variables seems promising (in Texel more than SBF), but high genetic correlations between variables may restrict the possibilities to change the growth curve shape. A random regression model was also fitted to the data to allow predictions of growth rates at relevant time points. Heritabilities for growth rates differed markedly at various stages of growth and between the 2 breeds (Texel: 0.14 to 0.74; SBF: 0.07 to 0.34), with negative correlations between growth rate at 60 d of age and growth rate at finishing. Following these results, future studies should investigate genetic relationships between relevant growth curve variables and other important production traits, such as carcass composition and meat quality.

Age Factors↗

Comparison of muscle fiber types from 2-year-old fillies of the Belgian, Standardbred, Thoroughbred, Quarter horse and Welsh breeds.

The percentages of three muscle fiber types in the biceps femoris and triceps brachii were determined in five breeds of horses: Belgians, Standardbreds, Thoroughbreds, Quarter Horses and Welsh ponies. Biopsies were taken from the two muscles from each of four 2-year-old untrained fillies of each breed. Percentages of red, white and intermediate fiber types were determined from tissues stained for succinic dehydrogenase activity. Intermediate fibers were the most numerous for all breeds. The difference between red and white fibers varied significantly with breed. Thoroughbreds had the highest percentage of red fibers and Belgians had the most white fibers.

Animals↗

Additive genetic and heterosis effects in crosses among cattle breeds of British, European and Zebu origin.

Breed and heterosis effects for maternal and calf components for weaning traits were measured in the progeny of Angus (A), Brahman (B) and Charolais (C) sires mated to A, B, C and reciprocal AB, AC and BC dams. Additive breed effects for the calf component for weaning weight were -3.0 +/- 3.2, -26.6 +/- 3.1 and 29.6 +/- 3.3 kg for A, B and C, respectively. Corresponding maternal breed effects were -1.7 +/- 2.4, 7.8 +/- 2.3 and -6.1 +/- 2.6 kilograms. Heterosis effects on weaning weight for the calf component were 21.2 +/- 3.6 for AB, 1.4 +/- 3.7 for AC and 16.5 +/- 3.4 for BC crosses, while heterosis levels for the maternal component were 28.9 +/- 2.7 for AB, 16.5 +/- 3.2 for AC and 18.7 +/- 2.9 kg for BC dams. The corresponding estimates for condition scores tended to parallel those for weaning weight. Approximate relative production efficiency rates were computed for the different mating groups as (calf weight divided by cow weight) x weaning rate. These values were .34 for purebred matings, .36 for purebred dams raising F1 calves, .40 for F1 cows raising backcross calves and .43 for F1 dams raising three breed crossbred calves.

Animals↗

Reproductive performance and profitability of heifers fed to weigh 272 or 318 kg at the start of the first breeding season.

Reproductive performance and weaning weight of the first calf was determined in 221 Brahman crossbred heifers fed to weigh either 272 (TW1) or 318 kg (TW2) at the start of their first breeding season (target weight). Heifers were divided into light- (below average) and heavyweight (above average) groups on the basis of initial weight. Within each target weight, heifers were fed in three lots. One lot contained lightweight heifers, the second contained heavy heifers and the third was composed of one-half heavy- and one-half lightweight heifers. Heifers were fed for 200 d before the start of the first breeding season. More heifers in TW2 showed estrus and became pregnant in the first 20 d of the breeding season and more were pregnant at the end of the first breeding season. These same differences in reproductive performance were also noted the second year. Each heifer exposed in TW2 weaned 43.4 kg more calf than those in TW1. An average heifer in TW2 was fed 220 kg more corn and 100 kg less hay than a corresponding heifer in TW1. Estrus and pregnancy rate for lightweight heifers in TW1 and TW2 were not improved by sorting and feeding them separately.

Animals↗

Genotype x environment interactions involving proportion of Brahman breeding and season of birth. I. Calf growth to weaning.

Performance to weaning was evaluated on 489 spring-born and 416 fall-born crossbred calves of three proportions of Brahman breeding (0, 1/4 and 1/2 Brahman) over a 3-yr period. The calves were produced by appropriate matings of Angus (A), Hereford (H), Brahman (B), 1/2B-1/2A and 1/2B-1/2H bulls to Angus and Hereford cows. Interactions between proportion of Brahman breeding and season of birth existed (P less than .01) for all traits except birth weight. Birth weights of 1/4 and 1/2 Brahman calves were 1.4 and 3.8 kg heavier (P less than .05), respectively, than 0 Brahman calves. Spring-born calves that were 1/4 and 1/2 Brahman outgained (P less than .05) 0 Brahman calves 36 and 69 g/d, respectively, and were 9 and 18 kg, respectively, heavier (P less than .05) at weaning, whereas preweaning average daily gains and weaning weights were similar among fall-born cross-bred calf groups. Among spring-born calves, 1/4 and 1/2 Brahman calves were 2.6 and 6.6 cm, respectively, taller (P less than .05) than 0 Brahman calves, whereas among fall-born calves 0 and 1/4 Brahman calves had similar hip heights and 1/2 Brahman calves were 3.7 and 2.8 cm taller (P less than .05) than 0 and 1/4 Brahman calves, respectively. Conformation and condition scores were similar for crossbred groups among spring-born calves, whereas conformation and condition scores decreased as proportion of Brahman breeding increased among fall-born calves. These data indicated that genotype X environment interactions are important in beef production and increased proportions of Brahman breeding were advantageous in a spring-calving program but not in a fall-calving program.

Animals↗

Influence of breed and diet on growth, nutrient digestibility, body composition and plasma hormones of Brangus and Angus steers.

Two split-plot designed experiments were conducted to determine the effects of breed (Angus, A, or Brangus, B) and diet (fescue hay, FH; corn silage, CS; or concentrate) on composition and rate of growth, diet digestibility and plasma hormones of steers. In Exp. 1, 10 steers (five of each breed) were fed a CS-based diet followed by a FH-based diet for two consecutive 60-d periods. Both breeds had lower (P less than .01) DM intake and digestibility when fed FH than when fed CS diets. The B steers had higher (P less than .01) plasma insulin concentrations than A steers when fed the CS diet. In Exp. 2, during two consecutive years, 10 steers previously fed CS- and FH-based diets were finished with a corn silage-whole shelled corn-based diet. During yr 1, A steers had higher (P less than .01) DM intake and plasma triiodothyronine (T3) and thyroxine (T4) concentrations (P less than .05) than B steers did. Although final weights were similar (P greater than .10), A steers had heavier (P less than .05) carcass weights than B steers did. During yr 2, A steers had higher (P less than .07) DM and starch digestibilities and higher (P less than .01) plasma T4 concentrations than B steers did. The greater (P less than .01) energetic efficiency of A steers was attributed to the greater rates of fat deposition during yr 2. Regardless of type of diet fed, A steers were more efficient at depositing energy. Higher circulating T4 concentrations of A than B steers may explain some of the physiological differences between these breeds.

Animal Feed↗

Initiation of the breeding season in a grazing-based dairy by synchronization of ovulation.

Lactating dairy cows (n = 228) in a semiseasonal, grazing-based dairy were subjected to artificial insemination (AI) to start the 23-d breeding season (d 0 to 22) followed by natural service (d 23 to 120). Cows were randomly assigned to: 1) Ovsynch (GnRH, d -10; PGF2,, d -3; GnRH, d -1; timed AI, d 0) followed by AI at estrus (tail paint removal) on d 1 to 22 (Ovsynch; n = 114); or 2) AI at estrus (tail paint removal) throughout 23 d of AI breeding (tail paint; n = 114). Days to first AI service were greater and the 23-d AI service rate was less for tail paint vs. Ovsynch cows (12.0 +/- 0.6 d vs. 0 d; and 84.2 vs. 100%, respectively). However, conception to first AI was greater for tail paint vs. Ovsynch cows (47.3 vs. 27.3%, respectively). Cows in the tail paint group received only one AI, during 23 d of AI, but 46.4% of Ovsynch cows received a second AI, with similar conception (43.1%) to that of tail paint cows at first AI (47.3%). Based on serum progesterone, incomplete luteal regression after PGF2alpha, and poor ovulatory responses to GnRH contributed to lower conception to timed AI in the Ovsynch group. Cumulative pregnancy rates for tail paint and Ovsynch cows did not differ after 23 d of AI breeding (47.3 vs. 46.3%, respectively) nor after 120 d of AI/ natural service breeding (80.5 vs. 83.3%, respectively). Lactating cows in this grazing-based dairy synchronized poorly to Ovsynch resulting in reduced conception to timed AI compared with AI after tail paint removal.

Animals↗

Short communication: predominance of beta-casein (CSN2) C allele in goat breeds reared in Italy.

A protocol for the rapid and simultaneous genotyping of A, C, and 0 'CSN2 alleles in goat was developed by single strand conformational polymorphism polymerase chain reaction (SSCP-PCR) technique. Screening the CSN2 variability in 7 goat breeds reared in Italy validated the genotyping test. The SSCP-PCR technique was also suitable for monitoring CSN2 polymorphism. In particular, the discrimination between CSN2*A and CSN2*C is important because the 2 corresponding protein variants cannot be separated by standard typing techniques. The monitoring of CSN2 variability in the goat breeds indicates the predominance of the C allele. In most breeds, CSN2*C occurred with the highest frequency, except in Saanen where CSN2*A and CSN2*C showed similar frequencies. Variant CSN2*C occurred with a frequency of 0.68 (Camosciata), 0.70 (Jonica), 0.71 (Garganica), 0.82 (Maltese), 0.87 (Cilentana), and 0.97 (Orobica). The alignment among the mature CSN2 sequences of different species suggests that CSN2*A is the ancestral allele compared with CSN2*C. Interestingly, the CSN2*A goat variant showed higher frequencies in selected breeds (Saanen and Camosciata).

Alleles↗

Genetic polymorphism of the epithelial mucin, PAS-I, in milk samples from the major dairy breeds.

Genetic polymorphism in a mucin of the human milk fat globule arises from variable numbers of a tandemly repeated amino acid sequence. As a consequence, the gene from each parent expresses a variable-sized protein. This is manifest on SDS gels in the form of either one or, more often, two protein bands, which differ among individuals in mobility. Evidence of such polymorphism in the bovine mucin, PAS-I, was first obtained from Holstein milk samples. The objective of this study was to evaluate the other major dairy breeds for polymorphism of their PAS-I. Milk samples from individual Jerseys, Guernseys, Ayrshires, and Brown Swiss were analyzed by SDS-PAGE. Bands of the mucin varying in number and mobility were seen in samples from all four breeds. In three of the breeds (Ayrshire, Brown Swiss, and Jersey), there was evidence that two alleles for PAS-I may have become predominant, possibly through degeneration in the structure of their tandem repeats, one that gives rise to a faster moving mucin (relative molecular weight 170,000) and the other to a slower form (relative molecular weight 200,000). In contrast, the PAS-I band patterns on SDS gels for both Guernseys and Holsteins were characterized in nearly 50% of samples by two close bands near the 205,000-molecular weight marker. This pattern was never seen in the other three breeds. The findings suggest a genetic kinship among the Ayrshire, Brown Swiss, and Jersey, on the one hand, and between the Holstein and Guernsey, on the other.

Alleles↗

Maximizing genetic response in breeding schemes of dairy cattle with constraints on variance of response.

Predicted genetic progress in dairy cattle breeding schemes was maximized with the variances of selection responses constrained, i.e., restricted effective population sizes. This restriction would also lead to schemes with acceptable rates of inbreeding (< .5%/yr). If the required coefficient of variation of the annual selection response was reduced from .32 to .16, numbers of animals selected, openness of schemes, and generation intervals increased. When elite cows produced 8 offspring annually, this reduction of the coefficient of variation tended toward a conventional progeny-testing scheme. If the number of donor cows was optimized, responses increased < or = 2%, and the breeding schemes became virtually closed. Variances of responses were reduced by selecting fewer, but proven, bulls, as is done in hybrid multiple ovulation and embryo transfer schemes, which select progeny-tested bulls and young elite cows. In spite of the constrained coefficients of variation, maximized genetic gains were high and were only reduced from .300 to .293 genetic standard deviations per year, when coefficients of variation were reduced from .32 to .16. Adoption of breeding schemes with low coefficients of variation is recommended, because responses are high and coefficients of variation are sensitive to accidental changes in the breeding structure.

Algorithms↗

Consensus and debate in the definition of breeding objectives.

The breeding objective is usually to increase the profit of the firm, industry, or society that is investing in a breeding program. This objective should include long-term genetic gain and nonadditive genetic changes such as inbreeding depression and possibly a weighting against the variability of outcome. The breeding objective is described by a profit function that takes genetic values as input and produces profit as outcome. This profit function may be a bioeconomic model of the farm. The traits in the profit function should relate as directly as possible to all sources of income and costs. The profit function can include variables controlled by management decisions if these interact with genetic merit. The differences between genotypes should be evaluated when management variables are optimized for each genotype. In the long term, mean profit is expected to be close to zero, and all costs are assumed to be variable costs. Under these conditions, the relative economic weights are the same, regardless of how the farm is constrained how the unit for which profit is calculated, whether the perspective is that of individual producers, an industry, or consumers. However, if price signals are not passed along the chain from consumers to seed-stock breeders, the economic weights become distorted. The use to which breeding objectives are put, the perspective from which they are calculated, the rescaling and biological versus economic objectives, and the special problems associated with the inclusion of length of herdlife in the objective are discussed.

Animals↗