Comparative effects of early weaning or once-daily suckling on occurrence of postpartum estrus in primiparous beef cows

We concurrently evaluated early weaning and once-daily suckling as options for shortening postpartum interval to estrus in primiparous cows calving in good body condition. Over 2 consecutive years, a total of 77 primiparous cows were assigned to 1 of 3 treatments: control (ad libitum suckling); once-daily suckling (for 30 d prior to start of breeding); or early weaning (calves weaned 30 d prior to start of breeding). All cows had a body condition score (BCS) of > or = 5 at parturition and were maintained in good condition throughout the breeding season. Cows were observed for estrus twice daily and blood samples for subsequent measurement of progesterone were collected at 48-h intervals. For data analysis, cows were divided into early- (> or = 85 d post partum) and late-calving (< 85 d post partum) groups at the onset of the breeding season. All calves were weighed at birth, at the onset of treatment, at weekly intervals until the start of the breeding season, and within 45 d of 205 d of age. Early weaning or once-daily suckling shortened the postpartum interval to first estrus of late-calving primiparous cows by 17 (P < 0.01) and 12 d (P < 0.08), respectively, compared with control group cows. However, among early-calving cows, neither early weaning nor once-daily suckling influenced the postpartum interval. Postpartum intervals of once-daily suckled cows and early-weaned cows were similar (P > 0.10).     

Reproductive performance of synchronized beef cows as affected by inhibition of suckling with nose tags or temporary calf removal

A study was conducted to determine whether presence of the calf during suckling inhibition influences the response to estrus synchronization in beef cows. Angus or Hereford cows (n=89) were administered Syncro-Mate-B (SMB), which consisted of a 6-mg norgestomet ear implant (in situ 9 d) in conjunction with 5 mg of estradiol valerate and 3 mg (im) of norgestomet. Cows were allotted by breed, body condition, stage of the estrous cycle, parity and date of parturition to 1 of 3 treatments: 48-h calf removal; ad libitum suckling; or inhibition of suckling with a nose tag for 48 h. Calves were weighed at time of SMB implant removal, 48 h later and at weaning. Cows were mated via AI approximately 12 h after detection of estrus during a 30-d period after implant removal followed by a natural service period of 35 d. At 48 h after implant removal, calf removal and nose tag calves had lost an average of 3.6 and 0.9 kg, respectively, while the suckled calves gained 1.8 kg (P < 0.01). Mean calf weight at weaning did not differ among treatments. Synchronized estrous response (within 5 d of implant removal) was not different among treatments. Pregnancy rate for cows exhibiting a synchronized estrus (5 d AI) for calf removal, nose tag and suckled cows was 76, 48 and 48%, respectively (P>0.10). Treatment did not affect the 30-d AI or overall 65-d pregnancy rate. In this study, there were no differences observed in the percentage of synchronized or pregnant cows following suckling inhibition by either a nose tag or calf removal. Transient reductions of calf body weight during the 48-h calf removal period did occur in both the nose tag and calf removal groups.     

Effect of restricted suckling on pregnancy rates and calf performance in Brahman cows

Seventy-six Brahman cows and first-calf heifers were assigned to one of two groups: 1) normal suckling (34 cows) or 2) twice-daily suckling (45 minutes of suckling each time; 42 cows). Twice-daily suckling was carried out from 30 days postcalving until weaning (seven months). All animals were maintained under artificial insemination for a four-month breeding period. Mean pregnancy rate was 63.06 +/- 0.06% and was influenced by suckling group (P<0.01) and number of parturitions (P<0.05). The pregnancy rates were 33% higher in twice-daily suckled cows. Forty-four percent of the first calf heifers in the twice-daily suckling group became pregnant compared to 9% in the normal suckling group (P<0.01). Twice-daily suckling improved pregnancy rate without depressing preweaning calf performance.     

Mechanical masking of neurosensory pathways at the calf-teat interface: endocrine, reproductive and lactational features of the suckled anestrous cow

A mammary somatosensory mask was employed in suckled anestrous beef cows to attenuate signals that were hypothesized to play a direct regulatory role in postpartum anestrus. Cows (n = 20) were randomly assigned to one of three treatment groups on Days 15 to 20 postcalving. The three treatments were: 1) masked (n = 7); 2) suckled (negative control, n = 6); and 3) weaned (positive control, n = 7). Four layers of surgical glove latex were used to cover the teats and ventro-lateral prominence of the udder of masked cows with a nonhardening, nontoxic adhesive (Day 0). Masks were designed to prevent direct contact between the skin of the teat/udder and the mouth of the calf and to allow normal suckling and milk removal. Masks were left in place for 7 d, with calves in the weaned group removed to a remote location for 7 d. Calves in the suckled group were allowed ad libitum suckling. Calves in the masked group tended (P < 0.1) to suckle longer than calves in the suckled control group (11.3 +/- 1.3 vs. 7.8 +/- 1.3 min/suckle) posttreatment; however, suckling frequency and calf weight gains did not differ due to treatment. Weaned cows exhibited a four-fold increase (P < 0.01) in the frequency of luteinizing hormone (LH) pulses on Day 2 relative to suckled and masked cows. The percentage of animals ovulating within 12 d after treatment differed (P < 0.05) and was 100, 50 and 0% for weaned, suckled and masked cows, respectively. Presence of the latex mask allowed essentially normal suckling and lactation, but failed to attenuate (and may have potentiated) the negative effects of suckling on secretory patterns of LH, ovulation and estrus.     

Effects of body condition and temporary calf removal on reproductive performance of range cows

The effects of body condition at calving and breeding and temporary calf removal prior to the start of the breeding season on reproductive performance of 323 cows from two breed groups were studied over two breeding seasons. Body condition score at calving was significantly and positively correlated with two body condition indices, which were based on weight-to-height ratio measured at calving and at the start of the breeding season. While the two body condition indices were strongly associated with the age of the cow, the body condition score, based on palpation and visual appraisal, was less affected by the age of the cow. Cows with a body condition score of 3.0 at calving had a shorter calving interval (P<0.02), higher pregnancy rate (P<0.08), and higher number of calves born (P<0.10) than cows which had body condition scores lower than 3.0 at calving. Temporary (48 h) calf removal prior to the start of the breeding season did not have a significant influence on the calving interval, pregnancy rate or the number of calves born nor on the weaning weights of their calves. Differences in reproductive performance between the two breed groups of cows were not significant.     

Synchronization of estrus in suckled postpartum beef cows with melengestrol acetate, 48-hour calf removal and PGF2alpha

One hundred and sixty-five suckled postpartum beef cows were utilized to evaluate the effectiveness of 2 estrus synchronization systems for the initiation and synchronization of estrus. The treatment groups consisted of 1) melengestrol acetate (MGA)-PGF2alpha (cows were given 0.5 mg MGA/head/day for 14 d with 25 mg PGF2alpha injected 17 d after the last day of MGA administration); 2) MGA-48-h calf removal (CR)-PGF2alpha (cows were given 0.5 mg MGA/head/day for 14 d with 48-h calf removal starting on the second day after completion of the MGA regimen plus 25 mg PGF2alpha administered 17 d after the last day of MGA); and 3) unsynchronized controls. Cows were assigned to treatments by the numbers of days post partum, body condition, age, and breed of sire. The cows were observed for estrus at 12-h intervals for 5 d after PGF2alpha administration and were artificially inseminated 12 to 18 h after the observed estrus. Both the MGA-PGF2alpha and MGA-CR-PGF2alpha treatments (64.8 and 61.8%) had greater (P < 0.05) 5-d estrus rates than the control treatments (34.5%). The synchronized pregnancy rate was greater (P < 0.05) for the MGA-CR-PGF2alpha than the control treatment.(52.7 vs 30.9%, respectively). The MGA-CR-PGF2alpha cows had a higher 25-d pregnancy rate than either the MGA-PGF2alpha (P < 0.05) or control cows (P < 0.08). Of the anestrous cows at the beginning of treatment, more MGA-CR-PGF2alpha (P = 0.1) and MGA-PGF2alpha cows were cyclic posttreatment than control cows (58.7 and 55.1 vs 44.7%, respectively), suggesting that treatment initiated estrous cycles in only a small number of the anestrous cows. Both MGA-PGF2alpha and MGA-CR-PGF2alpha treatments appear to be effective methods of synchronizing estrus in suckled postpartum beef cows. However, MGA-CR-PGF2alpha was more effective in establishing pregnancy earlier in the breeding season than MGA-PGF2alpha.     

The effects of conditioning to suckling, milking and of calf presence on the release of oxytocin in dairy cows

The aim of the study was to record the oxytocin (OT) release during milking (M) without or with calf presence, suckling (S) and finally calf removal just before the next milking in cows during postpartum or early lactation periods. Furthermore, the release of OT was examined during S and M in unknown surroundings (parlour). A total of 20 Brown Swiss cows kept under loose housing environment were used in our experiment. In both periods, the cows were milked twice daily at 07.00 and 18.00h and suckled three times daily at 09.00, 14.00 and 20.00h in the stall (tie housing). In the postpartum period, 13 cows were suckled and milked in the presence of their calves in the stall for the first 5 days of postpartum. Five from seven primiparous cows were additionally suckled by their own calves in the parlour on day 5 at 20.00h. On day 6, calves were separated and moved from mothers to the calf barn 10min before morning M. After evening milking cows were relocated to the herd within the same stable and milked in the parlour for a period of 4 weeks without contact to their calf. For control, additional seven primiparous cows without calf presence (not suckled) were also milked in the tie housing. In the early lactation period, suckled cows were moved back to the tie housing 2 days before the start of two consecutive days of S by their own calves and milking. Afterwards, 10min before M calves were separated again. Before S, two consecutive M were considered as controls. Results: The S stimulus during postpartum resulted in a higher OT release as compared with M in the calf presence and M after calf separation but not during M of not suckled cows. S in parlour reduced OT release. However, when not suckled primiparous cows were first milked in parlour, OT release was more reduced and in some cows total inhibition was observed. In early lactation during the first S, release of OT was lower than during control M, but increased gradually with repeated S and reached a maximum already on the second day. After two S, during evening M, the M related OT release was reduced as compared with controls. Calf removal 10min before M reduced OT release as compared with control M or M in calf presence. In conclusion, the calf presence and its removal can negatively influence OT secretion during M. Conditioning to machine milking caused a short-term reduction of OT release during first suckling, which normalised within 1 day.     

Influence of exogenous steroids, nutrition and calf removal on reproductive performance of anestrous beef cows

Methods for inducing a fertile estrus in anestrous beef cows suckling calves were explored in three studies. Trial 1 . Eighty-two primiparous and pluriparous Brahman-Hereford crossbred and Angus cows suckling calves were divided into four groups: 1) good body condition, high level of nutrition (GH); 2) good body condition, low level of nutrition (GL); 3) poor body condition, high level of nutrition (PH); 4) poor body condition, low level of nutrition (PL). All cows received the Shang Treatment (S). Following treatment, more cows (P<0.05) ovulated in the GH group (95%) than either the GL (61%), PH (58%), or PL (53%) group. Pregnancy rates were low and were not different between groups following the insemination taking place 54 hours after implant removal or after cows had been bred for 21 days. Trial 2 . One hundred fourteen two-year-old Santa Gertrudis-Hereford crossbred cows in poor body condition were divided into four groups. Forty-nine cows received S treatment and 65 cows served as controls (C) with approximately half of each group fed a high (H) or a medium (M) level of nutrition (SH, SM, CH, CM). One cow in the SH group ovulated and was pregnant 21 days after breeding. The remaining cows failed to exhibit estrus, ovulate or become pregnant. Trial 3 . Cows used in this trial were those from Trial 2 which did not exhibit estrus nor had a palpable corpus luteum present 21 days after implant removal. Cows were divided into 1) control (C), 2) wean (W), 3) wean + Syncro-Mate-B (W+SMB) and 4) Syncro-Mate-B + wean (SMB+W). The percentage of cows ovulating by 2 and 40 days after the start of breeding was similar (P>0.05) in the W, W+SMB, and SMB+W groups but all were greater (P<0.05) than the percentage of cows ovulating in the C groups. Pregnancy rates of cows in the W+SMB and SMB+W groups were higher (P<0.05) than pregnancy rates of cows in the W and C groups by two days after the start of breeding. Pregnancy rates 40 days after the start of breeding were higher (P<0.05) for cows in the W, W+SMB) and SMB+W groups than for cows in the C group.     

The effects of short term calf removal on pulsatile LH secretion in the postpartum beef cow

Patterns of secretion of LH were characterized before, during and after 72 h calf separation at approximately 30 days postpartum in nine suckled cows. Calf removal increased both LH concentrations and LH pulse frequency (P<0.01) in the period 48 to 56 h following calf removal in six acyclic cows, but no changes were seen in three cyclic cows. Calf return decreased LH concentrations and LH pulse frequency (P<0.05) within 8 h in the acyclic cows, but no changes were seen in the cyclic cows. Differences in the initial LH parameters and magnitude of the LH responses were apparent between the acyclic cows which responded to calf removal with progesterone secretion and those which did not. These data suggest that suckling inhibits the release of LH acyclic cows and that this is achieved primarily via a reduction in the number of pulsatile releases of LH.     

Ovulation, ovarian function, and reproductive performance after treatments with GnRH in postpartum suckled cows

Two experiments were conducted to determine whether treatments with gonadotropin releasing hormone (GnRH) during the early postpartum period in suckled cows would induce ovulation and initiate regular estrous cycles. In Experiment I, 0, 100 or 200mug of GnRH was given to 22 suckled Angus x Holstein cows at three and again at five weeks postpartum. Serum luteinizing hormone (LH) responses did not differ between cows given 100 or 200mug of GnRH. Treatment with GnRH tended to increase the percentage of cows exhibiting estrus by 30 and 60 days postpartum, but reproductive performance during the breeding season did not differ among groups. In Experiment II, 70 suckled Hereford cows were given either no treatment or 200mug of GnRH at 7 weeks postpartum. Cows given GnRH received either no treatment prior to GnRH or were separated from their calves for 24 hr prior to GnRH treatment. Half of the cows that were separated from their calves also received progesterone via a progesterone intravaginal device (PRID) for 12 days prior to calf removal. Treatment with GnRH alone tended to increase the percentage of anestrous cows which ovulated by 8 days after treatment. Calf removal did not increase the ovulatory response to GnRH, but PRID treatment did. More estrous periods were detected in GnRH-treated cows than in control cows during 20 days after GnRH treatment.     

Effects of supplementary feeding and suckling intensity on postpartum reproductive performance of small East African Zebu cows

Small East African Zebu cows (n = 120) which calved during the dry season were used to determine the effects of postpartum nutritional supplementation and suckling intensity on body weight, body condition score, reproductive performance and on calf mortality and preweaning growth performance. Cows were allocated based on calving body weight to either receive a supplementary feed of molasses blocks containing 10% urea or to serve as controls and to be grazed only. Within nutritional groups, cows were further assigned either to continuous suckling or to restricted suckling twice daily. Intact bulls were introduced 21 days after the first cow had calved, and data were collected for 8 months. Calving body weight and body condition score of dams ranged from 186 to 192 kg and from 3.8 to 4.2 and did not differ among the treatment groups. Supplementary feeding significantly (P<0.05) reduced calf mortality from 40 to 20%, while restricted suckling reduced mortality by 13% from 36 to 23%. Body weight and body condition score did not vary between groups during the supplementation period. Over the 8-month period, 65% of supplemented and 53% of control cows exhibited estrus (P>0.05). A significantly (P<0.05) karger percentage of restricted suckled cows showed estrus than of continuously suckled cows (74 vs 42%). The postpartum estrus interval was shorter by 54 days in supplemented than in control cows and by 13 days in restricted than in continuously suckled cows. The pregnancy rate was higher in supplemented than in control cows (37 vs 33%; P>0.05) and in restricted than in continuously suckled (46 vs 22%; P>0.05) cows.     

Beef cow reproduction as affected by postpartum nutrition and temporary calf removal

Data were collected on 306 multiparous cows over a 3-yr period (1984-1986) to evaluate the effect of postpartum nutrition and temporary calf removal on reproductive performance. All cows calved in a body condition score (BCS) of >/= 5 and were randomly allotted at parturition to an experiment with a 2 x 2 factorial arrangement of treatments. The factors consisted of high or low-flush levels of postpartum nutritional management, with or without temporary calf removal for 48 h prior to the breeding season. The high diet contained 26.0 Mcal metabolizable energy. The low regimen of the low-flush diet contained 14.7 Mcal metabolizable energy, with the flushing regime consisting of a diet of 36 Mcal metabolizable energy. The flushing diet was offered 2 wk prior to breeding through the first 30 d of breeding. Interval to estrus was 45 and 44 d for high and low-flush, respectively (P>0.05), while interval to estrus with temporary calf removal and without temporary calf removal was 47 and 42 d, respectively (P<0.05). Means for the cumulative percent in estrus at 20, 40 and 60 d of breeding, respectively, were high, 93, 97 and 98; low-flush, 95, 96 and 98; with temporary calf removal, 92, 96 and 99; and without temporary calf removal, 96, 97 and 98 (P>0.05). Interval to pregnancy was 81 and 82 d for high and low-flush, respectively (P>0.05), while interval to pregnancy with temporary calf removal and without temporary calf removal was 82 and 81 d, respectively (P>0.05). Cumulative percentages of animals pregnant at 20, 40 and 60 d of breeding, respectively, were high, 59, 83 and 91; low-flush, 59, 80 and 90; with temporary calf removal, 58, 83 and 91; and without temporary calf removal, 60, 80 and 90 (P>0.05). Calf performance in response to dam nutrition and temporary calf removal was not affected at weaning or at intervals prior to weaning (P>0.05). Interactions between nutrition level and removal of calf factors were not significant (P>0.05) for any of the parameters measured. The data suggest cows calving in BCS >/= 5 have equivalent reproductive performance whether receiving high levels of energy postpartum or low levels of energy early postpartum, followed by a flushing diet fed immediately proceeding and continuing through the first 30 d of breeding. No beneficial effect of temporary calf removal was observed for cows calving with BCS >/= 5.     

Reproduction in female yaks (Bos grunniens) and opportunities for improvement

This paper reviews seasonal breeding, puberty, postpartum anestrus, embryonic loss and calf survival and their constraints in female yaks. Methods for improving fertility in postpartum yak cows are also considered. Yaks are seasonal breeders with mating and conception restricted in the warm season. Puberty generally occurs in the 2nd to the 4th warm season following birth, i.e. between 13 and 36 months of age. The cows usually have a long postpartum anestrus period; only a small proportion of the cows return to estrus in the 1st breeding season after calving, most come into estrus in the 2nd and 3rd years. Nutritional status is the most important determinant of reproduction in female yaks. Reproductive success is a direct result of the availability of pasture determined by climate, season, and management practices. Milking delays puberty by reducing milk intake (restricted suckling) and growth rate for the calf. Milking interferes with grazing and prolongs the duration of postpartum acyclicity in cows. Calves born early in the season have a longer suckling season than those born later in the season before the onset of winter. Thus, they can have their first cycle in the breeding season of the following year, while those born late in the season may not have their first estrus until 25 or 26 months of age. Cows calving early in the season are more likely to return to estrus in the year of calving because they have a longer period to recover from the demand on body reserves before the onset of winter.Inbreeding in smallholder yak farms is also discussed and minimizing inbreeding by exchanging bulls among different herds is suggested. Reproductive efficiency can be improved by nutritional supplementation during the winter, however, the most cost-effective and practical strategy for this needs to be determined. Early weaning or restricted suckling may shorten the duration of postpartum acyclicity, however, it is impractical due to reduced growth rates and increased winter mortality of early weaned calves. A single treatment with either GnRH, or PGF(2alpha)+GnRH can successfully induce estrus in yak cows that calved in previous years (with or without calf) but did not calve in the current year, however, it has little effect in cows nursing a calf born in the current year. The effects of administration of exogenous progestogens plus GnRH on the fertility of yak cows are worthy of further study.     

Effect of calf removal on serum luteinizing hormone and cortisol concentrations in postpartum beef cows

Serum luteinizing hormone (LH) and cortisol concentrations were measured in ten fall calving, Angus cows averaging 38 +/- 8 days postpartum. Calves from five cows were weaned at the beginning of the study. Blood samples were collected at 20 min. intervals for 48 h after weaning and for 8 h on day 4 and day 6 postweaning. Mean serum LH concentrations increased (P<0.01) in weaned cows (W) from 0.55 +/- 0.01 ng/ml at time of calf removal to 1.3 +/- 0.04 ng/ml 48 h afterwards. Comparable LH concentrations for suckled cows (S) were 0.65 +/- 0.08 ng/ml and 0.62 +/- 0.03 ng/ml respectively. Average serum LH concentrations at 48 h after weaning were greater (P<0.01) for W cows than S cows and a treatment by time interaction occurred (P<0.01) with serum LH concentrations increasing (P<0.01) from time of calf removal to 48 h after calf removal in W cows. Frequency of LH peaks increased (P<0.01) in W cows and by 48 h after weaning was greater (P<0.01) in W cows than in S cows. Magnitude of LH peaks did not differ between the two groups. Serum cortisol concentrations were not different between W and S cows except for a transient elevation (P<0.01) in W cows from 7.6 +/- 0.9 ng/ml to 11.9 +/- 1.0 ng/ml 9 to 12 h after calf removal. Since serum LH concentrations were increased in W cows but not in S cows at 48 h and serum cortisol concentrations increased transiently in W cows we suggest that circulating cortisol levels may not be a physiological inhibitor of LH secretion in the suckled postpartum beef cow.     

Effect of bleeding stress and variable suckling intensity upon serum luteinizing hormone in Brangus heifers

In the first experiment, the effect of the stress of blood collection (via tail vessel puncture) on serum luteinizing hormone (LH) was evaluated in six nonsuckled first calf Brangus heifers. The animals were bled on days 22 and 31 postpartum at 15 minute intervals for a period of two hours. Blood was processed to yield serum and analyzed for LH via radioimmunoassay (RIA). There were no significant differences or fluctuations in serum LH levels between bleeding periods or between cows. Serum LH concentrations in nonsuckled cows were not affected by the stress of blood collection. In the second experiment, 24 first calf Brangus heifers were randomly assigned to one of four treatment groups. Treatment 1 cows were suckled once daily for approximately 30 min starting day 21 postpartum. Treatment 2 cows were suckled twice daily for approximately 30 min each time, starting 21 days postpartum. Treatment 3 cows were suckled once daily for approximately 30 min starting 30 days postpartum. Treatment 4 cows were suckled twice daily for approximately 30 min each time starting 30 days postpartum. Each cow was bled via tail vessel puncture on days one and nine following the start of each treatment. The blood sampling regime was similar to that used in Experiment 1 and consisted of four presuckling samples taken at 15 min intervals, one midsuckling sample (the calf was allowed to suckle for 15 min) and four postsuckling samples taken at 15 min intervals. Blood was collected, processed to yield serum and assayed for LH via RIA. Suckling intensity (SI) was found to have a significant effect on serum LH levels. The once daily suckled cows had higher (P<.01) mean serum LH levels than did the twice daily suckled cows (1.70 +/- .03 and 1.53 +/- .03 ng/ml, respectively). The LH concentrations decreased (P<.01) from the first to last bleeding time (BT). The mean serum LH levels for the presuckling, midsuckling and the first postsuckling samples were higher (P<.05) than the last postsuckling sample. The mean serum LH level for the first time period prior to suckling was higher (P<.05) than the last postsuckling sample. The mean serum LH level for the first time period prior to suckling was higher (P<.05) than the last two periods after suckling (1.73 +/- .08 ng/ml vs 1.51 +/- .06 and 1.41 +/- .06 ng/ml). Bleeding day (BD) and weaning day (WD) did not alter serum LH levels. The interactions found to be significant (P<.01) were SIxBD, SIxWD, BDxWD and BTxSIxBDxWD.     

Follicular growth and ovulation in postpartum beef cows following calf removal and GnRH treatment

This study investigated the effects of calf removal (CR) and gonadotrophin releasing hormone (GnRH) administration on the duration of the postpartum anoestrous period in suckled beef cows. Experiment 1 involved 20 multiparous suckled cows that were assigned to each of two treatments on Day 61 postpartum: (i) unlimited access to their calves (C; n=10) and (ii) calf removal for a period of 96 h (CR96, n=10). Experiment 2 involved 24 multiparous cows that were assigned to each of two treatments on Day 63 postpartum: (i) CR96 (n=12); and (ii) CR96 plus 250 microg of GnRH administered on the day before calf return (CR96+GnRH, n=12). Experiment 3 was a 3x2 factorial experiment, involving 48 multiparous cows assigned to the experiment on Day 58 postpartum. The factors were C, CR96 and calf removal for 144 h (CR144), and 0 or 250 microg GnRH administered on the day prior calf return. In Experiment 1, the number of cows that ovulated within 12 days of calf removal was higher (P<0.05) in CR96 group (3/9) compared to the C group (0/10). In Experiment 2, all 12 cows in the CR96+GnRH group ovulated. In contrast only 4/12 cows in the CR96 group ovulated in response to calf removal. The diameter of the ovulatory follicle tended (P=0.06) to be smaller in CR96+GnRH cows (9.8 +/- 0.3 mm) than in CR96 cows (11.3 +/- 0.9 mm). The maximum diameter attained by the corpus luteum (CL) also tended (P=0.08) to be smaller for cows in the CR96+GnRH than for cows in the CR96 group (12.1 +/- 2.4 mm versus 16.7 +/- 7.5 mm, respectively). Plasma progesterone concentrations 12 days after calf removal tended (P=0.06) to be lower in CR96+GnRH cows than in CR96 cows (0.66 +/- 0.1 ng/ml versus 2.00 +/- 1.1 ng/ml, respectively). Few cows in the CR96+GnRH group regained normal cyclical activity and the interval from onset of calf removal to conception was longer (P<0.05) compared to cows in the CR group (52.2 +/- 5.7 days versus 20.0 +/- 6.6 days). In Experiment 3, 5/8 cows on the CR144 group and all 8 cows in the CR144+GnRH group ovulated. However, the interval from CR to conception was similar for all treatments. Temporary (96-144 h) calf removal, particularly in combination with GnRH treatment, can induce a high proportion of beef cows to ovulate, but the restoration of oestrous cycles may not be achieved.     

Estrus and pregnancy after synchrony with lutalyse in conjunction with Syncro-Mate-B.

Estrous response and pregnancy rates are decreased for cows given Syncro-Mate-B (SMB) during metestrus (Day 1 to 5 of an estrous cycle). Data indicate these decreases are due, in part, to retention of a functional corpus luteum (CL). Our objective was to determine whether PGF2alpha administered in conjunction with SMB would improve estrous response and pregnancy rates in metestrous cows with no detrimental effects to cows in other stages of the estrous cycle. Three hundred seventy-three suckled beef cows were observed for estrus for 21 d before SMB administration to determine stage of an estrous cycle. Blood samples were collected 14 and 7 d before treatment and at SMB administration. Serum was assayed for concentration of progesterone to verify stage of estrous cycle or noncyclicity. All cows received the standard SMB regime and were allotted by age and stage of cycle to one of two groups. Cows denoted SMB + L received 25 mg of PGF2alpha 8 d after implantation, whereas cows denoted SMB served as controls. On Day 10, SMB implants were removed and females were observed for subsequent estrus. At this time, calves were removed from their dams for 48 h. Artificial insemination was performed 12 hr after observation of a standing estrus. Timed insemination was performed at 48 hr after implant removal for cows not inseminated at 24 or 36 hr after implant removal. Interval to synchronized estrus (within 5 d of implant removal) was lengthened for metestrous cows compared to cows in other stages of the cycle irrespective of treatment (P < 0.001). Cows receiving PGF2alpha had a greater pregnancy rate at 5 d compared to controls (P = .0672). Interval to estrus, estrous response, and pregnancy rate to A1 at d 28 or end of breeding season were not affected by administration of PGF2alpha in conjunction with SMB when compared to the standard SMB protocol.     

Effect of steroids and/or 48 HR calf removal on serum luteinizing hormone concentrations in anestrous beef cows

Serum luteinizing hormone (LH) concentrations were quantified in 27 thin, anestrous cows with suckling calves in each of three treatment groups: Syncro-Mate-B (SMB), 48 hr calf removal (CR), and SMB plus CR (SMB + CR). The SMB treatment consisted of a 9 day ear implant containing 6 mg norgestomet and an intramuscular injection containing 3 mg norgestomet and 6 mg estradiol valerate given at the time of implant placement. In the SMB + CR group, CR began at the time of implant removal (0 hr). Blood samples were collected every 4 hr via puncture of a tail vessel beginning 12 hr prior to implant and/or CR and continued for 72 hr thereafter. Before implant and/or CR (-12 to 0 hr), LH concentrations were higher (P<.01) in the CR (1.1 ng/ml) group than in the SMB (.6 ng/ml) and SMB + CR (.8 ng/ml) groups. Following implant and/or CR (4 to 48 hr), LH concentrations increased (P<.01) in the CR (1.8 ng/ml) and SMB + CR (1.3 ng/ml) groups, but remained unchanged in the SMB (.7 ng/ml) group. Furthermore, LH concentrations were higher (P<.05) in the CR group compared to the SMB + CR group. Circulating concentrations of LH declined (P<.01) to 1.2 ng/ml in the CR group following calf return, but remained unchanged in the other two groups. Although more (P<.01) cows in the SMB and SMB + CR groups were detected in estrus than in the CR group, there was no difference (P.10) in the number of cows ovulating between the three treatment groups. These results suggest that CR will increase circulating LH concentrations by 24 hr post CR and that SMB may partially suppress the CR induced LH release following implant and calf removal.     

Effect of monensin and suckling on the GnRH induced luteinizing hormone surge and the effect of monensin on the postpartum interval in Brangus cows

Twenty-seven fall calving Brangus cows were randomly allotted to one of four treatment groups: nonsuckled monensin (NSM), suckled monensin (SM), nonsuckled control (NSC), and suckled control (SC). Cows were group fed 1.82 kg/hd/day concentrate and Coastal bermuda grass hay $\text{ad}$$\text{libitum}$. Monensin cows received 200 mg monensin/hd/day in the concentrate. At 0800 hr on day 21 postcalving, the calves were separated from the cows. Suckled monensin and SC cows were allowed to suckle their calves for 30 min at 6-hr intervals. Nonsuckled monensin and NSC cows were not suckled. Calves were given free access to the cows after 1400 hr on day 22 postpartum. At 0800 hr on day 22 postpartum, a blood sample was collected. A 100 μg GnRH challenge was administered IM at 0801 hr. Blood samples were collected at 15-min intervals for 6 hr postinjection. Changes in body weight and body condition from day 21 postpartum to the day of first estrus were not different (P>0.10) by dietary treatment. Monensin cows consumed 10.7% less hay than did the control cows. Serum luteinizing hormone (LH) following GnRH was greater (P<0.005) in suckled than nonsuckled cows. Control cows released more (P<0.005) LH in response to GnRH than did the monensin cows. The postpartum interval (to first estrus) for the monensin cows (92.4±14.7 days) was shorter (P<0.025) than the controls (138.5±9.5 days). A greater proportion (P<0.005) of the monensin cows (8 of 14) exhibited estrus by 90 days postpartum compared to the control cows (0 of 13). Monensin and suckling appear to exert independent and agonistic influences on pituitary function in the postpartum beef cow.     

Effect of variable suckling intensity and estrogen administration upon serum luteinizing hormone in Brahman cows

Ten mature Brahman cows were randomly allotted within calving intervals to either a suckled (S) or nonsuckled (NS) treatment group. All cows received a 20 mg intramuscular injection of estradiol-17beta (E2), suspended in 2 ml of corn oil, to determine the effect of suckling on the estrogen induced LH surge. Starting on day 21 postpartum the S cows were suckled at six hour intervals for 24 hours, at which time they were challenged with a 20 mg E2 injection. The suckling regimen was continued for 48 hours postinjection. The NS cows were separated from their calves on day 21 postpartum and received no suckling stimulus for 72 hours. At 24 hours after calf separation, the NS cows were challenged with a 20 mg E2 injection. Blood samples were removed at two hour intervals beginning 10 hours post E2 injection until 36 hours postinjection, at which time blood samples were removed at four hour intervals until 48 hours postinjection. Blood samples were processed to yield serum and assayed for luteinizing hormone (LH) via radioimmunoassay. The injection of a 20 mg dose of E2 induced an LH surge in all cows. The NS cows were found to exhibit a longer (P<.05) duration of the estrogen induced LH surge than the S cows, 15.6 +/- .98 and 12.4 +/- .75 hours, respectively. The timing parameters (time to start of LH surge, time to peak LH value and time to end of surge) and LH concentration parameters (LH concentration at start of LH surge, peak value of LH surge and LH concentration at end of LH surge) were not different between suckling regimens. No blockage of the LH response to estrogen challenge was found on day 22 postpartum. Suckling did depress the duration of the LH surge indicating some blockage due to suckling stimuli.