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The standard procedure for assessing the breeding potential of a stallion includes the parameter total number of spermatozoa classified as morphologically normal. This study investigated sperm morphology of fresh semen in randomly chosen Estonian (E, n = 8) and Tori (T, n = 7) breed stallions with proven fertility. Two ejaculates were examined from each stallion. An aliquot from each ejaculate was fixed in 1 mL formol-saline immediately after collection and examined with phase-contrast microscope at a magnification 1000× for all types of morphological abnormalities. Furthermore smears were prepared and stained according to Williams (carbolfuchsin-eosin) for a more detailed examination of the sperm heads with light microscope at a magnification 1000×. Analysis of variance was applied to the data, and results are presented as LSmeans (± SE). One T stallion that had a disturbance in the spermatogenesis and one 22-year-old E stallion were not included in the analyses. The T stallions had on average 57.5 ± 4.1% and the E-stallions 74.4 ± 3.8% morphologically normal spermatozoa (p = 0.012). In 4 of 7 T stallions and 7 of 8 E stallions both ejaculates had >50% morphologically normal spermatozoa. There was a significant difference between breeds in mean percentage of proximal droplets (17.3 ± 2.7% and 2.9 ± 2.5% for T and E stallions, respectively; p = 0.003).

The objective of the study was to estimate genetic correlations between skin lesions and aggressive behavior postmixing and under more stable social conditions as a potential means of selecting against pig aggressiveness. Postmixing aggression in commercial pig production is common, compromises welfare and profitability, and cannot be significantly reduced by low-cost changes to the environment. A genetic component to individual aggressiveness has been described in pigs and other species. Selective breeding against aggressiveness ought to be possible if an easily measured indicator trait can be shown to be genetically associated with aggressive behavior. Aggressive behavior was recorded continuously for 24 h after mixing, and a count of skin lesions (lesion count, LC) was recorded at 24 h and 3 wk postmixing on 1,663 pigs. Two behavioral traits were found to have a moderate to high heritability similar to that of growth traits; duration of involvement in reciprocal fighting (0.43 [+ or -] 0.04) and delivery of nonreciprocal aggression (NRA; 0.31 [+ or -] 0.04), whereas receipt of NRA had a lower heritability (0.08 [+ or -] 0.03). Genetic correlations ([r.sub.g]) suggested that lesions to the anterior region of the body 24 h after mixing were associated with reciprocal fighting ([r.sub.g] = 0.67 [+ or -] 0.04), receipt of NRA ([r.sub.g] = 0.70 [+ or -] 0.11), and to a lesser extent, delivery of NRA ([r.sub.g] = 0.31 [+ or -] 0.06). Lesions to the center and rear were primarily genetically associated with receipt of NRA ([r.sub.g] = 0.80 [+ or -] 0.05, 0.79 [+ or -] 0.05). Genetic correlations indicated that pigs that engaged in reciprocal fighting delivered NRA to other animals ([r.sub.g] = 0.84 [+ or -] 0.04) but were less likely to receive NRA themselves ([r.sub.g] = -0.41 [+ or -] 0.14). A genetic merit index using lesions to the anterior region as one trait and those to the center or rear or both as a second trait should allow selection against animals involved in reciprocal fighting and the delivery of NRA. Positive correlations between LC 24 h and 3 wk after mixing were found, especially for lesions to the center and rear of the body, indicating that postmixing lesions are predictive of those received under more stable group conditions. As well as reducing immediate aggression at mixing, selection on postmixing LC is expected to have a long-term impact on injuries from aggression, even after dominance relationships are established. Key words: aggression, fighting, genetic correlations, lesion, pig

The objective of this study was to investigate factors that might influence the length of productive life in Swedish crossbred (Landrace x Yorkshire) sows. The data set consisted of 20,310 sows farrowing between 2001 and 2004 in 21 commercial piglet-producing herds. Productive life (PL) was defined as the number of days between first farrowing and removal or termination of data collection. In addition to the overall risk analysis of PL, another 4 longevity traits were analyzed (competing risk analyses): reproductive disorder-determined length of PL (RPL), udder problem-determined length of PL (UPL), lameness-determined length of PL (LPL), and mortality-determined length of PL (MPL). Analyses were performed by using survival analysis, applying a Weibull model with 6 time-dependent and 1 time-independent variable (age at first farrowing). The factor with the largest contribution to the likelihood function for PL was days after farrowing, followed by parity, the herd x year combination, the total number of piglets born, days between weaning and next farrowing, farrowing month, and age at first farrowing. For all 4 competing risk traits, the factors contributing most to the likelihood function were days after farrowing, the herd x year combination, and parity, with a varied order between traits. The hazard for removal was greatest 30 to 40 d after farrowing (after weaning) for PL, UPL, and LPL (P < 0.001). However, for MPL the hazard was greatest just after farrowing (0 to 10 d), and for RPL the hazard peaked at 70 to 100 d after farrowing. The hazard for removal was, compared with parity 1, less in parities 2 to 7 and greater from parity 8 for PL (P < 0.001). The hazard was greatest in parity 1 (P < 0.01) for RPL, UPL, and LPL, whereas for MPL the hazard increased with greater parity number and was markedly greater from parity 9 (P < 0.001). Sows with litters of 9 piglets or less had a greater hazard for removal than sows with litters of 12 to 13 piglets (P < 0.001). Intervals between 120 and 122 d from weaning to the next farrowing showed the lowest hazard for removal (P < 0.001). The influence of farrowing month displayed no clear pattern for PL. Sows of 14 mo or older at their first farrowing had a 20% greater hazard for removal than younger sows (P < 0.001). The hazard for removal was greater for smaller litters in all parities but was more accentuated in greater parities. Overall, days after farrowing was the main risk factor for sow removal. Removal hazard was greatest shortly after weaning, and this peak increased with greater parity number. Key words: longevity, mortality, removal reason, removal risk, sow, survival analysis

In a five-generation selection experiment, separate lines of standard mink (Mustela vison) were subjected to selection for litter size at 3 wk (F line), body weight in September (BS line), underfur density (P line), or combined selection for litter size and body weight (I line). One unselected line served as a control (C line). The present paper focuses on correlated responses to selection regarding fertility and fitness traits, fur quality, and body size traits. Genetic and environmental parameters were estimated with REML (Restricted Maximum Likelihood) techniques using a multi-trait, reduced animal model in a derivative-free way. Genetic and phenotypic correlations were estimated from four subsets of data consisting of 1) female September weight, litter size, and kit mortality; 2) body size traits; 3) September weight and fur traits graded on live mink; and 4) fur traits graded on live mink and skins. September weight was found to be negatively correlated with fertility and fitness traits as well as with fur traits. Selection for underfur density resulted in an improvement in guard hair quality and in general impression of the fur and almost eliminated the fur defect metallic sheen.

In a five-generation selection experiment, separate lines of mink (Mustela vison) were subjected to selection for improved litter size at 3 wk (F line), BW in September (BS line), and underfur density (P line), and combined selection for litter size and BW (I line). Underfur density was subjectively judged on live animals. One unselected line served as a control (C line). Significant changes were achieved in each trait: litter size in the last generation was 5.3 in the F line vs 3.7 in the C line; September weight in males was 2,254 g in the BS line vs 1,979 g in the C line, and the underfur density score, graded using a 5-point scale, was 4.1 in the P line vs 2.9 in the C line. In the combined line (I line) litter size was only slightly improved, whereas BW was substantially increased (male mean = 2,194 g). A univariate animal model was used to predict genetic values and to estimate variance components with a REML procedure. Heritability estimates were .14 |+ or -~ .09 for litter size, .39 |+ or -~ .06 for September weight, and .21 |+ or -~ .06 for underfur density. It was confirmed that the reproductive performance of heavy of fat animals was poor. Responses were higher than predicted when selecting for September weight and underfur density. In the last generation the average breeding values, relative to the base generation, were + .8 kits for litter size (F line), +365 g for male September weight (BS line), and +1 point for underfur density (P line). The study suggests that negative maternal effects on litter size may exist in mink.