Boars were heated for 6 h/day in a climate chamber (mean maximum temperatures, 33.4 +/- 3.1--37.7 +/- 2.0 degrees C, and relative humidities 40--80%) for 4, 5 and 7 days respectively (4 boars/group). Significant increases in the proportion of morphologically abnormal spermatozoa were seen in all groups for the end of Week 2 and up to Week 5 after treatment. Boars exposed for 7 days were, in general, more severely affected. Ejaculate volumes, gel volumes, sperm concentration and daily sperm outputs were not affected significantly in any of the groups, although changes were seen in individual animals. In some boars heat stress early in the treatment period produced an acute rise in body temperature which appeared to have a greater effect on semen quality than did the duration of exposure.

SUMMARY Sterile guarded swabs were used to sample the anterior vaginal and cervical area of 23 normal healthy sows during various stages of the reproductive cycle. The samples were collected one week before farrowing, within 24 hours of farrowing, weekly up to weaning, at mating and at 2 and 3 weeks after mating, and then plated and incubated aerobically and anaerobically. At least one positive sample was obtained from each sow and at each stage of the reproductive cycle. Most positive samples (78.3%) were obtained on the day of farrowing and the least 3 weeks after mating (19.0%). The second highest number of positive samples (45.5%) was found immediately after mating. Although there was no significant difference among sows of different parities, there was a trend for older sows to have more positive samples after farrowing (84.6%). There was a greater decrease in positive samples after farrowing and after mating among younger sows compared with older sows. A wide range of bacteria including aerobic and anaerobic species, were recovered from 142 Isolates. The more representative bacteria were Streptococcus spp (23.2%); Escherichia coll (22.5%); Staphylococcus spp (19.0%) and Corynebacterium spp (13.4%). Of the cultures, 54.7% were pure and 45.3% were mixed. Both the percentage of bacterial isolates as well as the type of culture (pure or mixed) were similar to those frequently reported in clinical cases of vulval discharge syndrome. The results indicate that sows usually develop infections of the reproductive tract at farrowing and mating but these infections do not normally persist.

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Abstract. The present study examined whether delipated porcine oocytes and embryos at various stages of development can be cryopreserved by conventional slow cooling or vitrification. Most (93%) of the 27 delipated morulae developed to blastocysts after freezing with 1.5 M propanediol + 0.1 M sucrose. Late morulae and early blastocysts delipated at 2-4 cell stage and cultured in vitro survived freezing either with 1.5 M glycerol + 0.25 M sucrose (10/18, 56%) or 1.8 M ethylene glycol + 0.25 M sucrose (14/19, 74%). Delipated 2-4 cell stage embryos and oocytes could be cryopreserved by vitrification with 40% ethylene glycol, 1 M sucrose and 20% fetal calf serum. Half (7/14) of the vitrified, delipated embryos developed to blastocysts after thawing. Of 48 delipated oocytes, 27 (56%) maintained an intact outline of the ooplasm after vitrification and underwent subzonal sperm injection. Fertilization was confirmed in 12 (25%) of these oocytes and 3 (6%) developed to morula stage. This study also aimed at developing a non-invasive method for cryopreserving porcine embryos after reducing their cytoplasmic lipid content without micromanipulation. Morulae and early blastocysts were centrifuged in the presence of cytochalasin B and cryoprotectants and then frozen immediately. More than half (14/24, 58%) of the centrifuged morulae developed to blastocycts after freezing with 1.5 M propanediol + 0.1 M sucrose. Greater than 70% of centrifuged early blastocysts survived freezing either with 1.5 M propanediol (30/31, 97%), 1.5 M glycerol (22/29, 76%) or 1.8 M ethylene glycol (21/29, 72%). These results demonstrated that delipation (lipid removal) from porcine oocytes and embryos at various stages enables their cryopreservation. A new insight into the development of a non-invasive method for cryopreserving porcine embryos was also provided.

Fifty-four Large White gilts were used to determine the effect of body composition at selection (145 d of age) on the onset of puberty and subsequent reproductive development until 202 d of age. Gilts were assigned to one of three groups based on their backfat depth at selection: 10 to 12 mm (L), 13 to 15 mm (M), and 16 to 18 mm (F). All of the F gilts, 92% of the M gilts, and 67% of the L gilts reached puberty by slaughter at 202 d of age. Data from a subgroup (first 67% to reach puberty in each group; L = Lp, M = Mp, and F = Fp) was also used. The M (Mp) and F (Fp) gilts reached puberty at 172 d (166 d) and 170 d (166 d) of age, respectively, but the L (Lp) gilts at 184.5 d were 12 d (18 d) older than M (P < .05), Mp (P < .001), and F (P < .01), Fp (P < .001) gilts. The Lp (97.68 kg) and Mp (98.33 kg) gilts were lighter (P < .01) than Fp (108.72 kg) gilts at puberty. There were no differences (P < .05) among the L, M, and F gilts in terms of backfat depth or weight at puberty. The L (Lp) gilts had a mean of 1.16 (1.75) estrous cycles, which was lower (P < .01) than for M (Mp) and (P < .01) F (Fp) gilts, with 1.96 (2.29) and 2.25 (2.33) cycles, respectively. L (Lp) gilts had fewer (P < .05) follicles, 13.14 (12.63), than either M (Mp), 19.08 (18.71), or F (Fp), 18.25 (17.42) gilts. The number of corpora lutea was not influenced (P > .05) by grouping at selection, but Fp gilts had fewer (P < .05) corpora lutea than Mp or Fp gilts. Live weight at slaughter was not influenced (P > .10) by grouping at selection or subgrouping at puberty. The L gilts with a mean of 18.05 mm of backfat at slaughter were leaner (P < .05) than the F (21.66 mm) but not (P > .10) the M gilts (19.41 mm). Subgrouping had no effect. Fat deposition and protein deposition were higher (P < .05) in those animals that attained puberty. We conclude that the rate of fat and protein deposition seems to be one of the determinants of puberty attainment.