Effects of stair-step nutrition and trace mineral supplementation on attainment of puberty in beef heifers of three sire breeds.

A study was conducted to evaluate the influence of nutrition and sire breed on age at puberty and first lactation milk yield in crossbred beef heifers. After weaning, 208 heifers sired by Hereford, Limousin, or Piedmontese bulls were assigned to either a control (CG) or stair-step gain (SSG) dietary regimen plus a mineral supplement with or without Cu, Zn, and Mn top-dressed onto the feed. Heifers on the SSG regimen were fed a diet intended to supply energy to support gains at a rate of 120% of the CG diet for 55 d and then were switched to a diet formulated to produce an ADG at 70% of the rate of the CG diet for 84 d. They then switched back to the 120% diet for the last 30 d before breeding. Total weight gain and overall rate of gain did not differ among dietary treatments. Hereford- and Limousin-sired heifers gained at similar rates, and Piedmontese-sired heifers gained an average of .10 kg/d slower than the other two sire breed groups. During one period, Piedmontese-sired heifers on the CG diet gained .19 kg/d faster ( P < . 01) when supplemented with mineral than when not. During that same period, there was no influence of mineral supplementation on weight gains for Hereford- or Piedmontese-sired heifers on the high SSG diet, but Limousin-sired heifers tended (P = .07) to gain faster (1.00 vs .85 kg/d) when supplemented with Cu, Zn, and Mn than when not. Piedmontese-sired heifers reached puberty at the earliest age (P = .03), followed by Hereford- and then Limousin-sired heifers. There were no treatment effects on milk yield at an average of 70 d of lactation. However, at approximately 120 d of lactation, Piedmontese-sired heifers were producing less milk (P < .05) than Limousin- but not Hereford-sired heifers. Hereford-sired heifers had lower (P < .05) plasma Cu concentrations than Piedmontese-sired heifers. There were no treatment effects on plasma Zn concentrations. Heifers sired by bulls of breeds that differ in potential muscularity differed in growth, reproduction, milk yield, and plasma mineral concentrations, but dietary treatments resulted in little to no differences in these variables.

Effect of nutritional management, trace mineral supplementation, and norgestomet implant on attainment of puberty in beef heifers.

We conducted a study to evaluate the influences of nutritional management, trace mineral supplementation, and exogenous progesterone on attainment of puberty in beef heifers. Heifers (n = 180) were assigned at weaning to blocks and treatments. Treatments included two dietary regimens (corn silage vs pasture + oatlage), trace mineral supplementation, and puberty induction strategy (with or without progestin implant). Heifers that received pasture + oatlage were managed on grass-legume pastures from October 14 until December 14 and were then placed in pens and fed an oatlage-based diet through May 1994. Heifers fed the corn silage-based diet were housed in pens throughout the study. Norgestomet was implanted in half of the heifers on April 11 for 10 d. Progestin implant increased (P < .05) the number of heifers that had attained puberty by the end of the study, compared with nonimplanted heifers (89% vs 71%). Trace mineral supplementation did not affect percentage of heifers that reached puberty before the implant period. Plasma copper levels were below recommended levels in heifers fed oatlage-based diets without trace minerals. We conclude that heifers can be placed on regrowth in irrigated pastures during the fall and still make acceptable gains for attainment of puberty the following spring and that progestin treatment can aid in inducing heifers to reach puberty.

Effect of age and pattern of gain on induction of puberty with a progestin in beef heifers.

Crossbred heifers (n = 75) fed for rapid (R; .82 kg/d) or slow-then-rapid (SR; .41 kg/d for 90 d then .82 kg/d) postweaning gain were used to examine the effects of age or pattern of gain on induction of puberty by a progestin. At 9.5, 11.0, and 12.5 mo of age, 12 prepuberal heifers from each growth treatment received progestin (a 6-mg Norgestomet implant for 10 d) or control treatments. Induction of puberty, LH secretory profiles, and ovarian follicular characteristics were assessed in Norgestomet-treated and control heifers. Body weights of R heifers were greater (P < .01) than those of SR heifers at all ages. At 12.5 mo, more Norgestomet-treated heifers exhibited a puberal estrus within 5 d after implant removal compared with controls (82% vs 9%, respectively), but Norgestomet did not induce puberty at 9.5 or 11 mo of age (progestin x age, P < .05) in heifers of either gain pattern. Norgestomet increased (P < .01) LH pulse frequency at all ages, whereas Norgestomet increased only mean LH concentrations at 12.5 mo of age (progestin x age, P < .03). Norgestomet treatment altered (P < .01) ovarian follicular characteristics at all ages. Gain pattern did not affect (P > .1) LH secretory profiles, ovarian characteristics, or induction of puberty by Norgestomet. We conclude that progestins induce puberty by hastening the normal cascade of endocrine and ovarian events associated with spontaneous puberty. Furthermore, age, but not pattern of gain, seems to be the critical factor influencing the efficacy of progestins to induce puberty in heifers.

Body composition and metabolic profiles associated with puberty in beef heifers.

Rapid growth large frame (RL, n = 61) or average growth medium frame (AM, n = 71) biotype heifers fed to achieve either moderate (MOD, .6 kg/d) or high ADG (HI, 1.0 kg/d) were used to determine whether puberty occurs at similar body composition or metabolic status. A heifer was considered pubertal after being detected in estrus and then forming a functional corpus luteum. Live animal estimates of body composition and blood samples for assessment of metabolic status were taken at 13 +/- .2 d after estrus for all heifers. Body composition and metabolic status were assessed every 56 d from 7 mo of age until puberty in a subset of 80 heifers representing all biotype-diet combinations. At puberty, 32 of these 80 heifers were slaughtered and physical and chemical composition of the empty body were determined. High-gain diet heifers were younger, heavier, taller, and more muscular (all P < .01) at puberty than MOD heifers. Slaughter measurements paralleled live animal estimates; bodies of HI and RL heifers contained more (P < .01) carcass and noncarcass components than those of MOD and AM heifers, respectively. Carcasses of RL and HI heifers were more (P < .05) muscular and fatter than AM and MOD heifers. At puberty, HI heifers had a greater (P < .01) mass of moisture, fat, and fat-free organic matter (FFOM) than MOD, whereas RL heifers had more moisture, ash, and FFOM than AM. Percentage of fat was greater (22.1 +/- 1.0 vs 1.0 vs 19.1 +/- 1.0; P < .05) and percentage of moisture was less (55.4 +/- .6 vs 58.1 +/- .6; P < .01) in bodies of HI than in those of MOD heifers. Concentrations of blood urea nitrogen and insulin were greater (P < .05) in HI than in MOD heifers. Diet did not influence concentration of IGF-I or glucose, and metabolic markers were unaffected by biotype. No dramatic changes in body composition or metabolic signals were detected before puberty. Puberty did not occur at similar body composition or metabolic status in all heifers.

The effect of estrus synchronization scheme, injection protocol and large ovarian follicle on response to superovulation in beef heifers.

Two trials were conducted to examine the effects of estrus synchronization scheme, gonadotropin injection protocol and presence of a large ovarian follicle on response to superstimulation of follicular development and the ensuing superovulation. Estrus was synchronized with either a progestin compound (MGA) or by the use of a luteolytic agent (PGF). Superstimulation was induced with 280 mg equivalents of pFSH administered either by a single subcutaneous injection or by a series of 8 intramuscular injections over 4 d. Follicular development was followed for 5 d with real-time ultrasound, and the heifers were retrospectively classified as to the presence or absence of a large follicle (> or = 8 mm; morphologically dominant follicle) at the start of superstimulation. The 2 trials differed by season of the year and genetic origin of the heifers. In Trial I (20 heifers), the ovulation rate was influenced by the 3-way interaction of the synchronization scheme, injection protocol and morphologically dominant follicle (P = 0.05). The number of large follicles on Day 5 (Day 0 = day of start of superstimulation) and ovarian score (scale 1 to 5 based on extent of follicular development; 1 = least, 5 = most) on Day 5 were significantly correlated (P < 0.05) with ovulation rate. In Trial II (20 heifers), the ovulation rate, number of embryos recovered, number of transferable embryos and ovarian weights were all greater (P < 0.05 to P < 0.01) with the 8-injection protocol than the 1-injection protocol. The number of medium follicles (5 to 7 mm) on Days 2 and 3, number of large follicles (> or = 8 mm) on Days 3, 4 and 5 and ovarian scores on Days 4 and 5 were all significantly correlated (P < 0.05) with ovulation rate. In both trials, differences in follicle populations were not seen until Day 3 of the superstimulation procedure. Collectively, these trials do not provide strong support for a single injection of FSH, as used here, nor does it indicate a clear advantage for either MGA or PGF as a means of enhancing the ovulation rate or embryo quality.

Endocrine responses in cows fed Ponderosa pine needles and the effects of stress, corpus luteum regression, progestin, and ketoprofen.

Pregnant cows were fed pine needles (PN, 2 kg.cow-1.d-1) mixed with the diet to determine factors that affect abortion response. In Exp. 1, treatments were used to determine the effects of experimental stress and pelleting of pine needles. Pelleting needles and experimental stress delayed abortion response (P < .01). Stress-induced delay was associated with abnormal patterns of progesterone and cortisol (P < .01). In Exp. 2A and 2B, the role of the corpus luteum (CL) in abortion response to PN consumption was investigated by regressing the CL with prostaglandin F2 alpha. Regression of the CL and PN feeding reduced interval to parturition, but the effect of PN feeding was less when the CL was regressed (PN x CL, P < .01). The progesterone increase in response to experimental stress was decreased by CL regression (P < .01). In Exp. 3, melengestrol acetate (MGA) was fed (0, 2, or 4 mg.cow-1.d-1) in addition to PN. Parturition was blocked more effectively as dose of MGA increased (P = .075), but only parturition was blocked rather than the effects of PN. In Exp. 4, CL regression was blocked by feeding ketoprofen. Ketoprofen delayed response to PN, but the effect was only temporary (P < .01). Our conclusions are that 1) experimental stress delays abortion response to PN by increased concentrations of progesterone, 2) pelleting PN decreases their abortifacient activity, and 3) abortions caused by PN can be blocked by feeding a progestin or a prostaglandin inhibitor, but these compounds do not block the primary abortifacient effects of PN.

Exercise and induced-parturition effects on dystocia and rebreeding in beef cattle.

The study involved 44 primiparous, 2-yr-old heifers and 74 multiparous cows, 3 or 4 yr old, bred to a single Charolais bull. Variables were dam age (heifer, H; or cow, C), restricted (RE) or forced (FE) exercise for the last 90 d precalving, and natural (NP) or induced (IP) parturition. The RE dams were held in drylots; FE dams were on range until d 260 to 267 and walked 3.2 km/d for feed and water. Dams with IP received 10 mg of flumethazone on d 269 of gestation. Diets for FE and RE dams contained the same hay and grain, but FE dams were fed in amounts projected to give weight changes approximating those of RE dams. All dams were calved in drylots; thereafter, all pairs were maintained together on pasture to the end of the study. Exercise did not affect dystocia score or incidence, increased feed requirement 31% (P < .01), and gave a 14.8% higher (P < .05) pregnancy rate in the subsequent 45-d breeding season. We hypothesize the increased pregnancy may have resulted from a feed-endocrine effect related to body weight gain, body composition-metabolic changes, or subsequent higher feed intake.(ABSTRACT TRUNCATED AT 250 WORDS)

Pine needle abortion in cattle: effects of diet variables on consumption of pine needles and parturition response.

Cows that consume needles from Pinus ponderosa (PN) abort, but little is known about variables that affect consumption or response. These experiments were conducted to test the effects of several variables on pine needle-induced abortion. Cows were placed on experiment at 250 d of pregnancy and were either given ad libitum (AL) access to PN separate from other feed sources or the PN were ground and fed (2 kg.cow-1.d-1) mixed with the diet. In Exp. 1, cows were assigned to a 2 x 2 factorial experiment with adequate (AP) vs high-protein (HP) diets and no straw vs AL straw (S). All cows ate PN and aborted, and there were no effects (P > .5) on interval to parturition (IP). Consumption of PN (kg/d) was increased by HP (P < .1). In Exp. 2, cows were assigned to five treatments to test the effects on response to PN of magnesium supplementation, weathering the PN, and using silage rather than hay as the basal diet. Consumption of PN shortened IP (P < .01), but magnesium, weathering PN, and silage-based diets did not decrease the response to PN (P > .5). In Exp. 3, cows were assigned to five treatments to test the effects of aging needles after they were ground, feeding bentonite, and feeding a complete mineral supplement. Pine needles decreased IP (P < .01), and the effects of PN were greater when PN were aged or bentonite or minerals were added (all P < .05).(ABSTRACT TRUNCATED AT 250 WORDS)

Sperm transport and distribution during the puberal transition in ewe lambs.

Sperm transport through and distribution within the anterior reproductive tract were evaluated at either 2 or 22 h after artificial insemination in ewe lambs at first (1E; n = 15) or third (3E; n = 14) estrus and in mature (MAT; n = 12) ewes. Each ewe was inseminated immediately upon detection of estrus with 7.5 x 10(8) progressively motile sperm placed into the external os cervix. Ewes were hysterectomized at either 2 or 22 h after insemination. Sperm were recovered from the uterus, isthmi, and ampullae by flushing with sterile .9% saline. The distribution of sperm recovered from the uterus, isthmus, and ampulla did not differ (P > .10) among 1E, 3E, and MAT ewes at either 2 or 22 h. However, there was a tendency (P = .08) for more sperm to be recovered from the anterior reproductive tract in 3E and MAT ewes than from that in 1E ewes. There was a time of hysterectomy x anatomical segment interaction (P < .05) for percentage of sperm recovered of the total number of sperm in the inseminate because more sperm were recovered from the isthmus and ampulla at 22 h than at 2 h after insemination. Percentages of 1E, 3E, or MAT ewes from which sperm were recovered from the anterior reproductive tract did not differ (P > .10). However, sperm were recovered from the oviducts in a greater (P < .05) percentage of ewes at 22 h after insemination than at 2 h.(ABSTRACT TRUNCATED AT 250 WORDS)

Effects of sire and dam on late-pregnancy conceptus and hormone traits in beef cattle.

Forty-six primiparous F1 heifers produced from mating Brahman (B), Charolais (C), Jersey (J), Longhorn (L), or Shorthorn (S) sires to crossbred cows were bred by AI to one of two Angus sires selected to produce high (H) or moderate (M) fetal growth. Dams were slaughtered at an average of 231 d of gestation. Daily blood samples were obtained from the dam on d 228 to 231 to determine serum estradiol, progesterone, and testosterone concentrations. Pelvic height was greatest (P < .05) in B, C, and L and pelvic width was greatest (P < .05) in S, C, and J dams, but pelvic areas did not differ (P > .10). Dams with greater hip height had larger pelvic areas (r = .45; P < .01). Intact fetuses from C and S dams were heaviest (P < .05), those from S dams had the greatest (P < .05) head width, and heart girth was greatest (P < .05) in fetuses from L dams. Fetuses from H sires were greater in weight (P < .01), body length (P < .01), and cannon circumference (P < .01). Dam differences were found in fetal heart weight (P < .01), trimmed placental membrane weight (P < .01), and average placentome weight (P < .05). Weights of eviscerated fetuses were greatest from C dams (P < .05). Placentome number was lowest (P < .05) in J dams, but J dams had the highest (P < .05) average placentome weight. Interactions between fetal genotype and breed of maternal environment were found for weight of eviscerated fetus (P < .05), body length, and heart weight (P < .01) and resulted from both magnitude and direction of change in the sire effect. The H sire increase in fetal weight was greatest in J dams, whereas B dams allowed expression of the fetal growth potential but at a lower level. Fetal trait interactions were also found for breed x sex and sex x sire (P < .05 to P < .01) and were due to the magnitude of differences expressed between the M and H sires. Serum testosterone concentrations were highest (P < .05) in B and L dams, dams gestating fetuses sired by the H sire (P = .08), and those with male fetuses (P < .01). We interpret these results to indicate that some maternal environments can suppress fetal growth, whereas others seem to complement the growth and allow maximum expression of the fetal genetic growth potential.(ABSTRACT TRUNCATED AT 400 WORDS)

Management considerations in heifer development and puberty.

Management of replacement beef heifers should focus on factors that enhance physiological processes that promote puberty. Age at puberty is important as a production trait when heifers are bred to calve as 2-yr-olds and in systems that impose restricted breeding periods. Calving by 24 mo of age is necessary to obtain maximum lifetime productivity. Because the reproductive system is the last major organ system to mature, factors that influence puberty are critical. The influence of environment on the sequence of events leading to puberty in the heifer is dictated largely by the nutritional status of the animal and related effects on growth rate and development. Management strategies have been designed to ensure that heifers reach a prebreeding target weight that supports optimum reproductive performance, and consequences of inadequate or excessive development have been evaluated. Those strategies are based on evidence linking postweaning nutritional development with key reproductive events that include age at puberty and first breeding, conception, pregnancy loss, incidence and severity of dystocia, and postpartum interval to estrus. Management alternatives that ultimately affect lifetime productivity and reproductive performance of heifers begin at birth and include decisions that involve growth-promoting implants, creep-feeding, breed type and(or) species, birth date and weaning weight, social interaction, sire selection, and exogenous hormonal treatments to synchronize or induce estrus. Basic and applied future research efforts should converge to match in a realistic manner the production potential of the animal with available resources. Strategies that incorporate consideration of nutrition, genetics, and emerging management techniques will need to be tested to enable producers to make decisions that result in profit. This review evaluates the current status of knowledge relating to management of the replacement beef heifer and serves to stimulate research needed to enhance management techniques to ensure puberty at an optimal age.

Effects of feeding ponderosa pine needles during pregnancy: comparative studies with bison, cattle, goats, and sheep.

Four experiments were conducted to determine the effect of feeding dried pine needles (Pinus ponderosa; PN) on the abortion rate of ruminants. In Exp. 1, cattle were fed 5.4 kg of PN daily for 21 d starting at 116, 167, 215, or 254 d of pregnancy. The PN did not cause abortions when started at 116 d; thereafter, the percentage of cows that aborted increased linearly, and the interval to abortion decreased linearly (both P < .01); all cows fed PN beginning at 254 d aborted. In Exp. 2, cattle were fed .7, 1.4, or 2.7 kg of PN for 21 d or 2.7 kg for 1 or 3 d. Sheep and goats were fed .8 and .5 kg of PN, respectively, starting at 121 d of pregnancy. The PN induced some abortions in cattle when fed for 1 (11%) or 3 (30%) d, but the abortion rate was greater (P < .01) when the PN were fed for longer periods of time (80, 90, and 100% aborted in 19, 17, and 10 d for .7-, 1.4-, and 2.7-kg doses, respectively). No goats or sheep aborted in response to PN feeding. Pregnancy rates during the next breeding season for cows that aborted in response to the PN were slightly higher than rates for control cows (94 vs 87%). In Exp. 3, buffalo (Bison bison) and cattle were fed 2.25 kg of PN from the same collection. Abortions were induced in all buffalo and cattle that were fed PN.(ABSTRACT TRUNCATED AT 250 WORDS)

Superovulation of cattle with equine pituitary extract and porcine ESH.

Superovulation has been practiced in cattle for more than 50 years but the results have been highly variable. Scientists at six locations compared a horse pituitary extract (HAP) with a single batch of porcine FSH (pFSH) to determine the efficacy of these hormones to induce superovulation and to test for variability in the superovulatory response. Acetone-dried equine pituitaries were suspended in 40% ethanol containing 6% ammonium acetate, and the supernatant was mixed with 2.5 volumes of cold ethanol. The resulting precipitate was washed with cold ether and dried. Total doses of 18 mg of HAP and 36 mg of pFSH were injected intramuscularly (i.m.) over 4 days, two injections per day, and prostaglandin (PGF(2)alpha; 25 mg, i.m.) was administered on Day 3. Injections were begun on Days 6 to 13 of the estrous cycle. The overall ovulation rates (mean +/- SEM) for HAP and FSH were 8.8 +/- 0.7 and 15.1 +/- 1.0, respectively (n=231; P<0.01). Location interacted (P<0.01) with the type of gonadotropin for the ovulation rate. When expressed as a proportion of the number of corpora lutea, the total number of embryos recovered was greater (P=0.03) for pFSH than for HAP, but there was no difference in the number of Quality 1 and 2 embryos. The results show that HAP can induce a satisfactory superovulatory response, but there was no evidence of reduced variability of response to HAP compared with pFSH.

Female traits, ovary and follicle characteristics, and the conditional probability of normal oocyte development after superovulation of beef cows.

The proportion of transferable beef embryos obtained after superovulation, follicle aspiration, and in vitro maturation and fertilization has been small. To seek possible explanations, cows on different planes of nutrition were treated with exogenous gonadotropin and oocytes were isolated from their ovaries. The record for each oocyte included characteristics of the follicle, ovary, and cow from which it was obtained and the response to in vitro maturation, fertilization, and development. The sample was used to obtain estimates of the relationships among the variables. The logistic function with the probability of normal development as the dependent variable was the basic equation of the statistical model. When an explanatory variable was itself a result of the biological system, an equation explaining variation therein was added to the model. Had equations representing endogenous regressors not been added to the model a simple, single equation would have represented oocyte development response; given an oocyte at aspiration only one variable, cumulus quantity, was found to condition the probability of normal development directly. However, the complete model included four additional equations: 1) the probability that an oocyte was recovered at aspiration was conditional on the plane of nutritional treatment and progesterone concentration in follicular fluid; 2) cumulus quantity was conditional on the presence on a corpus luteum, follicle size, and progesterone concentration; 3) progesterone concentration was dependent on plane of nutrition; and 4) corpus luteum was conditional on plane of nutrition. The estimated model provided some insight into the complexity of oocyte development response and the role nutrition may play.

Influence of sire, sex of fetus and type of pregnancy on conceptus development.

Estrus was synchronized in 93 crossbred cows 3 to 7 yr old which were then superovulated with 10 mg FSH-P and bred artificially to either a Jersey or Charolais bull. Females pregnant to the Jersey sire were slaughtered at 95, 180 or 250 d of gestation; low pregnancy rate from the Charolais sire resulted in enough dams for slaughter and valid comparisons at 95 d only. Conceptus tissue and organ weights and dam carcass weights and measurements were collected at slaughter. At 95 d of gestation, sire differences were not significant; type of pregnancy (single vs multiple) had significant effects on placentome and membrane weight; fetus sex had highly significant effects on fetus weight and crown-rump length. Fetal brain and heart weights showed little effect of sire, fetus sex or type of pregnancy, indicating these early differentiating tissues are highly competitive for available nutrients for growth. Fetal data at 180 and 250 d of gestation showed highly significant effects of gestation stage on placentome, membrane and fetus weights, crown-rump and metatarsal lengths, and liver, kidney, heart and total brain weights. Type of pregnancy had greater effects on the conceptus traits than did fetus sex at these stages. Nonorthogonal analyses of data from the Jersey-sired pregnancies indicated growth of fetuses in multiple pregnancies was suppressed, and the reduction in fetus weight became more pronounced as gestation progressed. Correlations among conceptus traits and dam carcass data showed different relationships within single and multiple pregnancies. We suggest that the genetic contribution for fetal growth has a positive effect on fetal size throughout gestation while the importance of metabolite availability may change during gestation depending on the genetic growth potential of the fetus and on whether the pregnancy is single or multiple. We speculate that these fetus-dam relationships involve systems controlling fetus growth that arise from the fetus genetic growth potential interacting with positive and negative dam effects that are linked or related to the carcass skeletal-fat-muscle endpoints studied.

Physiological mechanisms controlling anestrus and infertility in postpartum beef cattle.

Postpartum infertility is caused by four factors: general infertility, lack of uterine involution, short estrous cycles and anestrus. The general infertility component is common to any estrous cycle and reduces potential fertility by 20 to 30%. Incomplete uterine involution prevents fertilization during the first 20 d after calving but is not related to anestrus. Short estrous cycles prevent fertility during the first 40 d after calving by causing the cow to return to estrus before pregnancy recognition occurs. Anestrus is the major component of postpartum infertility and is affected by several minor factors: season, breed, parity, dystocia, presence of a bull, uterine palpation and carryover effects from the previous pregnancy as well as two major factors: suckling and nutrition. These major factors have direct effects on anestrus but also interact with one or more other factors to control postpartum anestrus. Physiological mechanisms associated with anestrus involve blockage of the GnRH "pulse generator" in the hypothalamus, but other pathways also must be involved because bypassing the pulse generator is not an effective treatment for all cows. The primary cause of anestrus probably is different for different stages of anestrus. The mediating mechanisms for anestrus are not involved with prolactin, oxytocin, the adrenal or direct neural input from the mammary gland but are at least partially involved with blood glucose and the endogenous opioid peptide system. Management options to decrease the impact of anestrus and infertility include: 1) restrict breeding season to less than or equal to 45 d; 2) manage nutrition so body condition score is 5 to 7 before calving; 3) minimize effects of dystocia and stimulate estrous activity with a sterile bull and estrous synchronization; and 4) judicious use of complete, partial or short-term weaning.

Pine needle abortion in cattle: associated changes in serum cortisol, estradiol and progesterone.

Nineteen spring-calving cows were used in an experiment to study the effect of feeding pine needles on incidence of premature parturitions (abortions) and the associated changes in serum cortisol, estradiol-17 beta and progesterone. The study was conducted over 2 years (1983, seven cows fed pine needles and three controls; 1984, six cows fed pine needles and three controls). Experimental feeding started at an average of 250 d of gestation and continued until parturition. Daily blood samples were taken from the start of feeding through 2 to 4 d after parturition. Feeding pine needles shortened gestation by 16 d and induced a premature normal rise in cortisol and estradiol-17 beta associated with parturition. Cortisol concentrations were also high at the beginning of the bleeding period and remained higher in pine needle-fed cows. An abrupt rise in progesterone concentration occurred after the start of pine needle feeding which then decreased sharply for 7 to 8 d before parturition and did not decrease to control concentrations until after parturition. We conclude that feeding pine needles to pregnant cows in late gestation causes abortions and that these abortions are directly caused by or are associated with changes in steroid metabolism.

Effects of induced parturition and early obstetrical assistance in beef cattle.

Pregnant crossbred beef females (33 second-calf cows and 73 primiparous heifers) bred to a single Hereford sire were assigned to a 2(3) factorial study involving age of dam, natural (NP) or induced (IP) parturition and late emergency (LA) or forced early (EA) obstetrical assistance. Parturition was induced with 10 mg flumethazone given i.m. between 1400 and 1600 on d 272 of gestation; EA was given when the cervix and birth canal were fully dilated. Average IP occurred 39.6 h postinjection, and 95.3% of the treated dams responded within 60 h postinjection; gestation was shortened 2.9 d (P approximately equal to .07). Dystocia score (from 1 = no assist to 4 = major traction required and 5 = abnormal presentation) was 1.12 vs 2.40 for LA and EA, respectively (P less than .01), and 11% of LA vs 84% of EA were assisted. Calf vigor score (1 = normal to 3 = severely depressed or dying) at birth was 1.3 for NP and 1.1 for IP (P approximately equal to .06) and 1.3 for EA and 1.1 for LA (P less than .05). This effect of EA was due to reduced vigor of calves experiencing abnormal presentation. Birth weights (BW) and weaning weights (WW) of calves from cows exceeded those from heifers (32.6 vs 30.8 kg, P less than .05; 210.9 vs 156.3 kg, P less than .01, respectively). Differences due to IP and EA in BW, WW, postpartum interval and conception rate were not significant, but weight gain of calves from EA dams tended (P approximately equal to .09) to be greater than weight gain of calves from LA dams.(ABSTRACT TRUNCATED AT 250 WORDS)

Progesterone concentrations in beef heifers bred at puberty or third estrus.

Peripheral serum progesterone concentrations were evaluated in beef heifers following breeding collected on d 6 +/- 1, 9 +/- 1 collected on d 6 +/- 1, 9 +/- 1 and 12 +/- 1 (estrus = d 0) after the puberal estrus of all heifers and after the third estrus of E3 heifers. Progesterone concentrations were higher (P less than .05) for heifers in E1 compared with heifers in E3 on d 6, 9 and 12 after breeding to a fertile bull. Progesterone concentrations on d 6, 9 and 12 did not differ (P greater than .10) between pregnant heifers in E1 and E3; however, non-pregnant heifers in E1 had higher (P less than .05) concentrations of progesterone compared with non-pregnant heifers in E3 on each day. Concentrations of progesterone did not differ (P greater than .10) between non-pregnant heifers in E1 and heifers of E3 during their puberal cycle. Pregnant heifers in E1 and E3 had higher (P less than .05) concentrations of progesterone on each day than non-pregnant heifers in their respective treatments. There were no interactions (P greater than .10) between treatment, pregnancy status and day-of-estrous cycle for concentrations of progesterone. Results of this study indicated that luteal function differed between heifers that failed to conceive at their puberal estrus and heifers that failed to conceive at third estrus. However, concentrations of progesterone did not differ between heifers that conceived at puberal or third estrus. The relationship of changes in luteal function from the puberal through the third estrous cycle and pregnancy is not clear.

Pregnancy rates of beef heifers bred either on puberal or third estrus.

The objective of this study was to determine if pregnancy rates (PR) differed between beef heifers bred to fertile bulls on either their puberal (E1, n = 89) or third (E3, n = 67) estrus. Heifers were obtained from two lactations (Manhattan, L1; and Miles City, L2), and the experiment was conducted at Miles City. Heifers were assigned randomly within location to either E1 or E3. Heifers were fed to gain .56 kg.head-1 X d-1 and observed twice daily for estrus. After exhibiting first estrus (puberty) and breeding, each heifer in E1 was palpated rectally on d 6, 9 and 12 +/- 1 d (estrus = d 0) for the presence of a corpus luteum, and a venous blood sample was collected for assay of progesterone by radioimmunoassay. Heifers in E3 were palpated and bled on the same schedule as heifers in E1 after first estrus and after being bred to a fertile bull at third estrus. Pregnancy rates were determined by rectal palpation at approximately 38 d post-breeding. Location of origin did not affect (P greater than .10) weight at puberty or weight at breeding; however, heifers from L1 were younger (P less than .05) than heifers from L2 at puberty and breeding. Pregnancy rates were 57 and 78% for heifers in E1 and E3, respectively (P less than .05). Weight at breeding did not influence (P greater than .10) pregnancy rates. The probability of heifers in E1 becoming pregnant increased (P less than .05) with increasing age, while age was not a factor (P greater than .10) for heifers in E3. These results indicated that fertility of puberal estrus in beef heifers is lower than third estrus. Higher fertility of third estrus may be related to maturational changes associated with cycling activity.