Breeding soundness examinations of rams and bucks, a review.

Breeding soundness examinations of rams and bucks may be performed by veterinarians as a service for clients. A physical examination for breeding soundness includes a general examination for health with special consideration of the reproductive organs. Careful examination of the penis, prepuce, and testicles may reveal diseases or abnormalities which decrease reproductive potential. Rams with small or hypoplastic testicles are unsatisfactory potential breeders as testicle size is positively related to sperm production. Libido may be assessed during semen collection procedures or from observations of the owner. Semen quality may be evaluated using tests for motility, concentration, and morphology of spermatozoa. Rams may be declared satisfactory, questionable, or unsatisfactory potential breeders as a result of the examination.

Effect of presence of the male on initiation of estrous cycle activity of goats.

Serum progesterone concentrations and behavioral estrus were determined in two groups of 17 mixed breed dairy does at the beginning of the breeding season. The treatment group was pastured adjacent to two mature bucks while two teaser bucks ran with the group. The control group was pastured without exposure to bucks. Goats were observed for estrus daily for 35 days and samples of jugular blood were collected every other day for radioimmunoassay of progesterone. Signs of estrus were observed in 16 of 17 does in the treatment group within a mean +/- S.E. of 5.5 +/- 1.3 days after introduction of the bucks. Thirteen does demonstrated a progesterone profile characteristic of a normal estrous cycle with peak progesterone concentrations of 5.9 +/- 0.5 ng/ml. Signs of behavioral estrus were not observed in the control group. One control doe demonstrated a progesterone profile characteristic of a normal estrous cycle attaining a peak progesterone concentration of 3.9 ng/ml. Progesterone concentrations in the remaining 16 control does were at or near the lower limits of sensitivity of the assay for the duration of the experiment. Fifteen of the control does exhibited estrus within 7 +/- 1.5 days after exposure to bucks at the end of the experiment. These results clearly demonstrated a profound influence of the male on estrous cycle activity during the beginning of the breeding season.

Fertility of goats following synchronization of estrus with prostagland in F2alpha.

Thirty-four mixed breed cyclic does were randomly divided into two groups of 17 each. One group was synchronized for estrus using two i.m. injections of 8 mg PGF2alpha administered 11 days apart. The other group served as controls and was bred at the time of naturally occurring estrus. Both groups were bred by natural service. Ninety-four percent of the treated does came into estrus within a mean (+/- S.E.) of 53 +/- 3 hours after the second injection of 8 mg PGF2alpha. No differences (P > 0.10) in the first service conception rates based on radiography at mid-gestation were observed between the treated and control groups. It was concluded that the use of 8 mg injections of PGF2alpha 11 days apart had no detrimental effects on fertility of goats.

Doses of prostaglandin F(2)alpha effective for induction of estrus in goats.

A total of 11 cycling does weighing between 24 and 50 kg were injected with varying dosages of prostaglandin F(2)alpha (PGF(2)alpha) between 7 and 10 days into each estrous cycle. Five injections each of 1.25, 2.5, 5.0, or 7.5 mg PGF(2)alpha were alternated with five injections of 1.0 ml saline. Saline treated does served as controls. All does were teased twice daily with a buck and observed for signs of estrus for 5 days post-injection. Daily systemic concentrations of progesterone (P(4)) were determined by radioimmunoassay. The mean (+/- S.E.) hours from injection to estrus was 47 +/- 3.3, 42 +/- 4.3, 44 +/- 8.5, and 43 +/- 5.5 for does receiving 1.25, 2.5, 5.0, and 7.5 mg PGF(2)alpha, respectively. None of the does receiving saline exhibited estrus in the 5-day post-injection observation period. Mean (+/- S.E.) concentrations of systemic P(4) in all does on the day of injection was 4.22 +/- 0.45 ng/ml. Concentrations 24 hours post-injection were 0.21 +/- 0.02, 0.15 +/- 0.05, 0.17 +/- 0.04, 0.16 +/- 0.04, and 4.5 +/- 1.36 ng/ml for does receiving 1.25, 2.5, 5.0, and 7.5 mg PGF(2)alpha, and 1.0 ml saline, respectively. The results suggested that 1.25 mg PGF(2)alpha was effective for induction of estrus in the cycling goat.

Absence of sexual dimorphism in the goat: Induction of luteinizing hormone discharge in the castrated male and female and in the intersex with estradiol benzoate.

Gonadectomized male (n = 5) and female (n = 5) and intact intersex goats (n = 2) were injected i.m. with 50 mug 17(beta)-estradiol benzoate (EB). After treatment, there was a transient 6- to 9-hr decrease in circulating levels of LH followed by a preovulatory-like discharge of LH in all goats. Release peaked at 12 to 18 hr after EB treatment. The magnitude of discharge and the time from treatment until peak of release were not influenced by the goat's sex. These findings suggested that the positive feedback effects of estrogen on LH release were not sexually differentiated in the goat. Since tonic concentrations of LH prior to EB treatment were not different among the groups, the studies also suggested that the intersex goats lacked the inhibitory gonadal influences on gonadotropin release that characterize intact animals.

Incidence and treatments of postpartum reproductive problems in a dairy herd.

Incidence of assisted births, retained fetal membranes (RFM), and metritis were recorded in one hundred dairy cows from parturition through 14 days post-calving. Manual removal of RFM was not attempted. All RFM were excised inside the vulva and observations of natural RFM expulsion were recorded. Fifteen of 100 cows (15%) had assisted births, 27 (27%) had RFM, 8 (8%) had primary metritis not associated with other postpartum reproductive problems, and 26 (26%) had secondary metritis. Uterine swabs for culture were collected during the study from cows with postpartum reproductive problems. E . coli was the most common organism isolated (69.4%). Sensitivities of all isolates to penicillin, tetracycline, and triple sulfa were 44.0%, 59.5%, and 36.9% respectively. One of two antibiotic treatments were administered to cows with these postpartum reproductive problems. Treated animals received either 5 g. tetracycline powder IU on day 1 of treatment plus 10.5 million units procaine penicillin G IM on days 1, 2, and 3; or 4 Sulfaurea boluses IU on day 1. Despite the antibiotic treatments, 26 of 34 cows having either assisted birth and/or RFM developed metritis (76%). Neither treatment regimen was superior to the other. The poor results of antimicrobial therapy suggested the futility of routine administration of therapeutic agents for postpartum reproductive problems. Treatment failure was attributed to ineffective drugs or inadequate dosage regimens.

The effect of method of GnRH administration and short-term calf removal on ovarian function and reproductive performance in postpartum suckled beef cows administered PGF(2)alpha for estrous synchronization.

The first experiment was a 2 x 2 factorial experiment with calf removal (none or short-term) and method of GnRH administration (intramuscularly in saline or subcutaneously in gelatin capsules) as main effects. The durations of the GnRH-induced LH surges were similar among groups but the LH surges were delayed in the cows that received GnRH subcutaneously in gelatin capsules. Calf removal enhanced the GnRH-induced LH release for cows administered GnRH subcutaneously in a gelatin capsule but not for cows administered GnRH intramuscularly in saline. In the second experiment, 191 postpartum suckled beef cows were administered two injections of prostaglandin F(2)alpha(PGF(2)alpha) 11 days apart. After the second PGF(2)alpha injection, the cows were assigned to a 2 x 2 factorial experiment as in Experiment 1 plus one control group. Short-term calf removal (47 h) began 28 h after the second PGF(2)alpha injection. GnRH was administered 30 h after the time of calf removal. The number of cows that ovulated following the time of the GnRH treatment, the number that had abnormal luteal phases and the first-service pregnancy rates among treatment groups within the anestrous and cyclic cows classifications were not significantly different. However, several effects were detected and are reported.

Growth and ovarian function of weanling and yearling beef heifers grazing endophyte-infected tall fescue pastures.

Growth and ovarian function of crossbred beef heifers grazing low and high endophyte-infected tall fescue pastures were studied for 2 successive years. In April of each year, 20 weanling and 20 yearling heifers were included in the study. All heifers were weighed at 28-d intervals for 112 d. Blood samples were collected from each heifer on Day 0 and +7 of each of five 28-d periods and analyzed for progesterone concentration. Heifers with progesterone concentrations >/= 1.5 ng/ml on either or both Day 0 and +7 were classified as having normal cyclic ovaries. High endophyte-infected fescue pastures adversely altered the ovarian activity (P < 0.05) of weanling heifers in both years. In each trial, average weight gains were lower (P < 0.05) in yearling and weanling heifers grazing the high endophyte-infected pastures than in heifers grazing low endophyte-infected pastures. In 1992, heifers were synchronized with PGF(2alpha) administered on Days 101 and 112. Blood samples were collected on 0, 4, 8 and 12 d after the second PGF(2alpha) injection for progesterone analysis. Heifers grazing high and low endophyte-infected pastures were pastured separately with 4 bulls each and were given heatmount detectors. At 96 h, less estrus activity was observed (P < 0.10; power=0.63) in weanling heifers grazing the high vs. low endophyte pastures although pregnancy rates were similar for all groups. Progesterone concentrations suggested that weanling heifers on the high endophyte pastures had a higher incidence of luteal dysfunction after PGF(2alpha) synchronization. In summary, high endophyte-infected pastures decreased growth in both weanling and yearling heifers, ovarian activity and luteal function were adversely altered in weanling heifers with subsequent decreased estrus response to estrus synchronization.

Effects of bull exposure on the cyclic activity of beef cows.

In Experiment I, 38 crossbred suckled beef cows grazing fescue pastures and 34 crossbred beef cows grazing bluestem pastures were randomly allocated at the time of calving into a group with 4 teaser bulls or no bulls. Two blood samples were collected 7 d apart from the cows to determine cyclic activity 67 and 76 d after calving in the fescue and bluestem pastures, respectively. Progesterone greater than 1.0 ng/ml in one or both samples indicated cyclic activity. There was no difference in the percentage of cows cyclic among the different groups. The number of cyclic cows in the fescue pasture with bulls was 16/19 (84%); in the fescue pasture with no bulls, 14/19 (74%); in the bluestem pasture with bulls, 17/17 (100%); and in the bluestem pasture with no bulls, 16/17 (94%). Overall cyclic activity among all cows for teaser bull-exposed and no bull was similar, 33/36 (91%) and 30/36 (83%). Overall cyclic activity was greater (P < 0.05) in cows grazing bluestem (33/34), 97% than fescue pastures (30/38), 80%. Measurements of cyclic activity were initiated too late in the postcalving period to quantify differences in estrous activity between the bull and no bull treatment groups. Another trial was planned for the following year with a modified protocol. In Experiment II, blood samples were collected for progesterone concentrations soon after calving and were repeated at intervals to characterize both the occurrence and duration of estrous cycles. In this experiment, 29 crossbred suckled beef cows grazing fescue pastures were randomly allocated 12 d after calving (Day 0) into 1 of 2 groups with teaser bulls or without bulls. Nineteen crossbred beef cows grazing bluestem pastures were allocated similarly 10 d after calving (Day 0). Bulls were added to the groups with bulls in fescue and bluestem pastures on day 6 after the initial allocations. Blood samples were collected from all cows on Day 0 and every 3 d until Day 46. Means (+/- SEM) of the cumulative progesterone concentrations (ng/ml) per cow for the 16 samples from cows grazing fescue were 12.5 +/- 3.5 for cows exposed to bulls, 2.5 +/- 0.16 for cows not exposed to bulls, 27.6 +/- 4.42 for cows grazing bluestem pastures and exposed to bulls, and 16.0 +/- 2.75 for cows without exposure to bulls. Progesterone concentrations were higher in cows exposed to bulls (P < 0.01). The percentages of both short and normal cycles increased (P < 0.01) in groups exposed to bulls (88%, 21/24 and 63%, 15/24) when compared with the no bull groups (29%, 7/24 and 21%, 5/24), respectively. Cows exposed to bulls also showed increased cyclic activity.

The effect of short term calf removal in combination with GnRH treatment and the effect of limited nursing on reproductive performance of postpartum suckled beef cows administered PGF2alpha for ovulation control.

Over a two year period, postpartum suckled Hereford and Angus Cows (n=213) were administered two injections of PGF2alpha (25 mg/injection) and divided into three groups. No additional treatments were administered to cows in Group I and calves were allowed to nurse their dams ad libitum. In Group II, calves were removed for 48 hours beginning on the third day following the initial PGF2alpha injection. These cows were given a subcutaneous injection of 250 microg GnRH dissolved in 2% carboxymethylcellulose midway through the 48 hour period. In Group III, calves were allowed to nurse their dams for only one hour per day for the first 7 days after the initial PGF2alpha injection. In year 1, PGF2alpha was administered 14 days apart whereas in year 2, PGF2alpha was administered 11 days apart. Cows were artificially inseminated at 72 and 96 hours after the second injection of PGF2alpha. In year 1, the numbers of cows that conceived to the timed inseminations were similar (P>.10) for the three groups. In year 2, a higher percentage of cows in groups II (P<.10) and III (P<.05) conceived to the timed inseminations than in group I. Other reproductive performance parameters were similar (P>.10) between groups for both years 1 and 2. In summary, limited nursing and short term calf removal in conjunction with GnRH treatment may improve the pregnancy rate in cows administered PGF2alpha for ovulation control.

Effects of repetitive norgestomet treatments on pregnancy rates in cyclic and anestrous beef heifers.

Sixty-eight 12- to 14-month-old crossbred beef heifers averaging 285 kg were assigned at random to treated (n = 35) and control (n = 33) groups to evaluate the use of repetitive norgestomet treatments. Treated heifers received an ear implant containing 6 mg norgestomet on two occasions 16 days apart. Injections of 3 mg norgestomet and 5 mg estradiol valerate (EV) were given intramuscularly the same day as first implantation (Syncro-Mate-B). Implants were removed after eight days. Four bulls were then placed in each of two pastures containing half of the treated and half of the control heifers for 24 days after the time of the first implant removal. Progesterone concentrations from blood samples collected prior to the first treatment were used to determine reproductive status. The overall pregnancy rate 64 days after first implant removal for treated anestrous heifers (61%; 14 23 ) was similar (p > 0.25) to untreated (73%; 11 15 ) and treated (75%; 9 12 ) cyclic heifers, but higher (p < 0.1) than for untreated anestrous heifers (33%; 6 18 ). This treatment advantage resulted from an increased (p < 0.01) pregnancy rate after the second implant removal. In summary, repetitive norgestomet treatments enhanced pregnancy rate in anestrous heifers within a 24-day breeding season.

Norgestomet and gonadotropin-releasing hormone enhance corpus luteum function and fertility of postpartum suckled beef cows.

In Exp. 1,101 suckled beef cows were administered two injections of prostaglandin F2 alpha (PGF2 alpha) 11 d apart. Cows in Group 1 received no additional treatment. Cows in Groups 2 and 3 received 250 micrograms of GnRH plus 47-h calf removal. Cows in Group 3 also received a norgestomet ear implant that was inserted 4 d after the first PGF2 alpha injection and left in situ for 8 d. The second PGF2 alpha injection was administered approximately 28 h before the time of norgestomet implant removal. The GnRH was administered approximately 30 h after the time of norgestomet implant removal (or 58 h after the second PGF2 alpha injection). Calf removal was the period from the time of implant removal to AI. All cows were artificially inseminated once 75 h after the second PGF2 alpha injection (47 h after implant removal). Reproductive status before the time of GnRH treatment (presynchronization) was determined by multiple sampling (2, 13, and 23 d before GnRH treatment) for blood progesterone concentrations (62% anestrous and 38% cyclic). The GnRH treatment increased (P < .01) the ovulation response and norgestomet reduced (P < .01) the incidence of short luteal phases in the presynchronization anestrous cows. Norgestomet treatment increased (P < .05) the timed breeding pregnancy rates for both presynchronization anestrous and cyclic cows. In Exp. 2, 174 suckled beef cows were administered Syncro-Mate B (which includes norgestomet). Cows in Group 1 received no additional treatment, whereas cows in Group 2 received 250 micrograms of GnRH (30 h after norgestomet implant removal).(ABSTRACT TRUNCATED AT 250 WORDS)

Effect of hyperalimentation on body composition in swine.

Fifty growing pigs were used in two experiments to evaluate the effects of cannulation and hyperalimentation on performance and body composition responses. Surgical implantation of a cannula into the greater curvature of the stomach and subsequent management associated with maintenance of the cannula did not result in a reduction (P > .05) of voluntary feed intake. Cannulation did not negatively affect gain (P > .05). Over the entire trial, feed efficiency was not changed by cannulation (P > .05). Cannulation itself did not affect protein or fat deposition (P > .05) in the carcass. Hyperalimentation to approximately 120% of control intake resulted in increased daily gain (P < .05) and similar feed efficiency (P > .05) compared with that of control animals. Hyperalimentation decreased protein deposition (P < .05) and tended to increase fat deposition.

Performance and health of weanling bulls after butorphanol and xylazine administration at castration.

A total of 268 crossbred, 6- to 9-mo-old, bull calves (214 +/- 19 kg) were used in two separate 27-d experiments to assess the effects of butorphanol and xylazine administration (BXA) on the subsequent performance and health of beef calves. In each experiment, calves were randomly allotted to four treatment groups: 1) castration with BXA, 2) castration without BXA, 3) no castration with BXA, and 4) no castration without BXA. There were two replicates within each experiment. The intravenous administration of .07 mg/kg of butorphanol and .02 mg/kg of xylazine occurred 90 s before tail hold and castration procedures. Calves were placed in a squeeze chute and manually restrained by tail elevation. In Exp. 2, the cattle also were scored for chute activity (on a 1 to 5 scale with 5 being the most active). Cattle were weighed at the beginning and end of the experiment, feed intake was recorded daily, and cattle were monitored daily for respiratory disease. There were no castration x BXA interactions (P greater than .51). Castration reduced (P less than .01) daily gain and gain/feed and tended (P = .13) to reduce feed intake. The administration of BXA had no effect (P greater than .05) on gain or gain/feed but did tend (P = .13) to reduce feed intake. No differences (P greater than .45) were observed in morbidity or mortality due to either BXA or castration. Castration and BXA increased (P less than .01) blood cortisol levels on d 3, whereas control animals had reduced cortisol levels.(ABSTRACT TRUNCATED AT 250 WORDS)

Effect of interval from melengestrol acetate to prostaglandin F2 alpha on timed and synchronized pregnancy rates of beef heifers and cows.

The objective of this experiment was to determine the optimal interval from the last day of melengestrol acetate (MGA) feeding to prostaglandin F2 alpha (PGF2 alpha) treatment on pregnancy rates of beef heifers and cows. All females (149 heifers and 399 postpartum cows) were fed MGA (.5 mg) daily for 14 d and then administered PGF2 alpha (25 mg Lutalyse) 13, 15, and 17 d (Groups 1, 2, and 3, respectively) after the last day of MGA feeding. Females not in estrus the first 52 h after PGF2 alpha treatment were artificially inseminated 72 h after PGF2 alpha treatment. Females in estrus 0 to 52 h and 78 h to 6 d after PGF2 alpha treatment were inseminated at estrus. Blood sera (collected immediately before and 3 d after PGF2 alpha treatment) were assayed for progesterone concentrations. Pregnancy was determined 44 to 47 d after the 72-h AI by rectal examination. The intervals from MGA feeding to PGF2 alpha that had the highest 72-h AI pregnancy rates were 17 d for heifers (43%) and 15 d for cows (43%). Heifers with a 17-d interval had a higher (P < .05) 72-h AI pregnancy rate than heifers with 13-d and 15-d intervals, and cows with a 15-d interval had a higher (P < .05) 72-h AI pregnancy rate than cows with a 17-d interval. The 4-d synchronized pregnancy rates (the 72-h AI and the succeeding 3 d inseminations) for both heifers (44%) and cows (53%) were not different (P > .05) among groups. Fewer (P < .05) cows with a 17-d interval from MGA to PGF2 alpha had corpora lutea regression (by 72 h) after PGF2 alpha treatment than cows with 13-d and 15-d intervals. We interpret the results to indicate that the interval from MGA to PGF2 alpha treatment may influence 72-h AI pregnancy rates, that optimal intervals are 17 d for heifers and 15 d for cows, and that pregnancy rates are improved by insemination for 3 d after the 72-h AI.

Induction of luteolysis in goats with prostaglandin F2 alpha.

On day 10 of each estrous cycle, 19 cycling does were given (IM) 1 of 3 dosage levels of prostaglandin F2 alpha (PGF2 alpha) or saline solution. After injections, goats were observed twice daily for behavioral estrus, and serum concentrations of progesterone (P4) were determined from daily blood collections to measure response to treatment. Every dose of PGF2 alpha (0.0165 mg/kg of body weight, 0.0275 mg/kg, and 0.0385 mg/kg) was administered during 20 estrous cycles, and 0.25 ml of saline solution was administered during 12 estrous cycles. Fourteen of 20, 15 of 20, 20 of 20, and 0 of 12 does exhibited signs of behavioral estrus within 96 hours of injections of 0.0165 mg of PGF2 alpha/kg, 0.0275 mg of PGF2 alpha/kg, 0.0385 mg of PGF2 alpha/kg, and saline solution, respectively. A decline in mean concentrations of peripheral P4 from 3.6, 3.8, 4.4, and 4.3 ng/ml to less than 1 ng/ml within 24 hours was observed in 15 of 20, 16 of 20, 20 of 20, and 0 of 10 does after injections of 0.0165 mg of PGF2 alpha/kg, 0.0275 mg of PGF2 alpha/kg, 0.0385 mg of PGF2 alpha/kg, and saline solution, respectively. The dosage level of 0.0385 mg of PGF2 alpha/kg (1.75 mg of PGF2 alpha/45.36 kg) was effective for induction of estrus in 100% of the does.

Abnormal spermatozoa, testicular degeneration, and varicocele in a ram.

A 4-year-old Corriedale ram, with a history of infertility, had 50% abnormal acrosomes in the ejaculate resembling knobbed spermatozoa. Electron microscopic profiles of the apical segment of the affected acrosomes revealed a membrane-enclosed inclusion or cyst filled with particulate matter. The abnormal acrosomes were combined with a high prevalence of other degenerative changes such as head abnormalities, proximal droplets, and loose heads. Spermatozoa were examined from 9 ejaculates collected over an 8-month period. Abnormal acrosomes decreased to 5% after 4 months, but increased to 83% a month later. Examination of the testes after castration revealed bilateral varicocele and degeneration of seminiferous epithelium.

Peripheral serum progesterone and luteinizing hormone concentrations of goats during synchronization of estrus and ovulation with prostaglandin F2 alpha.

Prostaglandin F2 alpha (PGF2 alpha) (2 doses, 11 days apart) was given to 20 mixed-breed dairy does to synchronize estrus and ovulation. The dose of PGF2 alpha used was the free-acid equivalent of 8 mg which was divided between 2 injections at 0800 and 1200 hours. At the initiation of treatments, does were from day 0 (estrus) to day 18 of the estrous cycle. Seventeen of the doses exhibited estrus within a mean (+/- SE) interval of 53 +/- 2 hours after the first 0800-hour injection. Peripheral progesterone concentrations determined at daily intervals indicated that PGF2 alpha was luteolytic as early as day 4 of the cycle. Does were in the 8th to 12th days of the cycle at the time of the 2nd treatments with PGF2 alpha. Estrus was observed in all 20 does at 50 +/- 1 hour after the 0800-hour injections. Serum progesterone concentrations confirmed that luteolysis occurred in all of the does. In 19 does, concentrations of luteinizing hormone characteristic of a preovulatory peak were observed 55 +/- 2 hours after the 2nd 0800-hour injection. One doe did not demonstrate a luteinizing hormone peak within the 72-hour period. Laparotomies were performed 6 days after estrus, and ovaries were examined for corpora lutea. The mean number of corpora lutea was 2.0 +/- 1.0.

Effect of washing on motility and acrosome morphology of frozen-thawed goat spermatozoa.

Semen from 4 bucks was collected using an artificial vagina and was pooled and divided into 6 aliquots. Three aliquots were washed twice, 15 minutes each time, with Ringer's solution, and the fluid was removed by centrifugation at 950 X g between washes. All 6 aliquots (3 washed and 3 unwashed) were extended with skim milk-glycerol, lactose-egg yolk-glycerol, or tris (hydroxymethyl) aminomethane-citric acid-egg yolk-glycerol and were frozen in straws to -196 C. The semen was then thawed and kept at 37 C for 8 hours. Percentage of sperm motility was estimated, and the percentage of normal acrosomes (NA) was determined at 0, 2, 4, 6, and 8 hours after thawing. The experiment was repeated 7 times. The data indicated a significant positive effect (P = 0.0009) of washing on motility, but no effect (P = 0.5347) of extender. There was also a significantly higher percentage of NA in washed semen (P less than 0.0001). Sperm extended in tris aminomethane-citric acid-egg yolk-glycerol had more NA than those extended in lactose-egg yolk-glycerol. Sperm motility and acrosome morphology were depressed also in the presence of seminal plasma for the milk extender, which did not contain egg yolk. Removal of seminal plasma from goat semen was beneficial in preserving the integrity of the spermatozoa after freezing, regardless of the extender used.

Prevalence of Trypanosoma theileri in cows and fetuses at slaughter.

Blood from 171 pregnant and 65 nonpregnant cows was taken at slaughter for culture and examined during the culturing period for Trypanosoma theileri once a week for 5 weeks. Of the 171 fetuses from the pregnant cows, 119 (69.6%) were greater than or equal to 4 months gestation; blood samples from these fetuses were also taken for culture. Of 236 cows (81 of 171 [47.4%] pregnant and 20 of 65 [30.8%] nonpregnant cows), 101 (42.8%) were culture positive. More of the pregnant than nonpregnant cows were culture positive (P less than 0.05). More beef cows (48.0%) than dairy cows (34.1%) were culture positive (P less than 0.025). Two of the 119 (1.7%) fetus samples were found culture positive. The percentages of positive cultures from Brucella-reactor cows, 18 of 40 (45.0%), and from non-Brucella-reactor cows, 83 of 196 (42.3%), were similar. However, both of the culture-positive fetuses were from Brucella-reactor cows.