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Biomedical subjects

R A Bellows

Publications and source records attributed to R A Bellows.

At least 19 recordsLinked to original sources

Genetic parameter estimates for scrotal circumference and semen characteristics of Line 1 Hereford bulls.

The objectives of this study were to estimate heritability for scrotal circumference (SC) and semen traits and their genetic correlations (rg) with birth weight (BRW). Semen traits were recorded for Line 1 Hereford bulls (n = 841), born in 1963 or from 1967 to 2000, that were selected for use at Fort Keogh (Miles City, MT) or for sale. Semen was collected by electroejaculation when bulls were a mean age of 446 d. Phenotypes were BRW, SC, ejaculate volume, subjective scores for ejaculate color, swirl, sperm concentration and motility, and percentages of sperm classified as normal and live or having abnormal heads, abnormal midpieces, proximal cytoplasmic droplets (primary abnormalities), bent tails, coiled tails, or distal cytoplasmic droplets (secondary abnormalities). Percentages of primary and secondary also were calculated. Data were analyzed using multiple-trait derivative-free REML. Models included fixed effects for contemporary group, age of dam, age of bull, inbreeding of the bull and his dam, and random animal and residual effects. Random maternal and permanent maternal environmental effects were also included in the model for BRW. Estimates of heritability for BRW, SC, semen color, volume, concentration, swirl, motility, and percentages of normal, live, abnormal heads, abnormal midpieces, proximal cytoplasmic droplets, bent tails, coiled tails, distal cytoplasmic droplets, and primary and secondary abnormalities were 0.34, 0.57, 0.15, 0.09, 0.16, 0.21, 0.22, 0.35, 0.22, 0.00 0.16, 0.37, 0.00 0.34 0.00, 0.30, and 0.33, respectively. Estimates of rg for SC with color, volume, concentration, swirl, motility, and percentages of live, normal, and primary and secondary abnormalities were 0.73, 0.20, 0.77, 0.40, 0.34, 0.63, 0.33, -0.36, and -0.45, respectively. Estimates of rg for BRW with SC, color, volume, concentration, swirl, motility, and percentages live, normal, and primary and secondary abnormalities were 0.28, 0.60, 0.08, 0.58, 0.44, 0.21, 0.34, 0.20, -0.02, and -0.16, respectively. If selection pressure was applied to increase SC, all of the phenotypes evaluated would be expected to improve. Predicted correlated responses in semen characteristics per genetic SD of selection applied to SC were 0.87 genetic SD or less. If selection pressure was applied to reduce BRW, the correlated responses would generally be smaller but antagonistic to improving all of the phenotypes evaluated. Predicted correlated responses in SC and semen characteristics per genetic SD of selection applied to BRW were less than 0.35 genetic SD.

Animals↗

Effects of severity of dystocia on cold tolerance and serum concentrations of glucose and cortisol in neonatal beef calves.

Effects of dystocia on rectal temperature and serum cortisol and glucose concentrations, were studied in neonatal calves exposed to 0 degree C. Primiparous dams were observed continuously during parturition and if Stage II (labor) was not completed within 2 h after appearance of the allantochorion, delivery was completed with obstetrical assistance. Parturitions were scored (CDS) for difficulty and obstetric assistance required: CDS 1, no assistance (n = 8); CDS 2, minor manual assistance (n = 7); CDS 3, use of a mechanical calf puller (n = 5); CDS 4, cesarean section (n = 6). A blood sample, rectal temperature, and body weight were obtained within 30 min after birth. Calves were then fed 38 degrees C pooled colostrum, muzzled to prevent suckling, and placed back with their dam in a heated (22 degrees C) barn. At 4 h of age an indwelling jugular catheter was inserted. At 5 h of age calves were placed in a 0 degree C room for 140 min and blood samples and rectal temperatures were obtained every 10 or 20 min. A shivering score (1 = no shivering; 2 = moderate shivering; 3 = intense shivering) was assigned at each sampling time. Rectal temperatures were higher (P < 0.01) in CDS 1, 2 and 4 calves (39.0, 39.3, and 39.0 +/- .02 degrees C, respectively) than in calves with CDS 3 (38.3 +/- 0.02 degrees C) and were affected by duration of cold exposure (time; P < 0.01). Shivering was not affected by CDS but was affected by time (P < 0.01). Glucose concentrations were higher (P < 0.01) in CDS 3 calves (110.1 +/- 1.6 mg/dL) than in CDS 1, 2, or 4 calves (77.2, 86.4, and 89.0 +/- 1.3 mg/dL, respectively) and changed over time (P < 0.01). Cortisol concentrations were higher in CDS 1 calves (80.0 +/- 1.7 ng/mL) than in CDS 2, 3 or 4 calves (62.7, 58.2, and 57.7 +/- 2.0 ng/mL, respectively) and were affected by time (P < 0.01). We conclude that severe dystocia (CDS 3) resulted in lower calf rectal temperature, reduced serum cortisol, and increased serum glucose which could affect the ability of the calf to withstand cold stress. Minor dystocia did not cause and timely cesarean delivery prevented, the physiological aberrations encountered in severe dystocia.

Adaptation, Physiological↗

Effects of dietary fat and sire breed on puberty, weight, and reproductive traits of F1 beef heifers.

Prepubertal F1 heifers (n = 246; from crossbred dams bred to either Hereford [H], Limousin [L], or Piedmontese [P] sires) were fed 1.9% (LF) or 4.4% (HF) dietary fat from 254+/-4 d of age until they reached puberty or the breeding season started. Safflower seeds (37% oil with 79% linoleic acid) were the added fat source. Blood samples and backfat thickness measurements were obtained from 60 randomly selected heifers representing the sire breeds and diets studied. In addition, five H-sired heifers from both diets were serially bled at 28-d intervals. Total gain, ADG, body condition score, and backfat thickness were affected by sire breed (P < 0.001) but not diet. Backfat thickness was affected (P < 0.01) by the diet x time on feed interaction. Diet did not affect pubertal age (P > 0.10) but tended (P = 0.08) to affect the percentage of heifers pubertal by the beginning of breeding (June 4). Sire breed effects on puberty age at beginning of breeding, percentage pubertal at the beginning of breeding, and puberty age during the entire study were all highly significant. The effect of the diet x sire breed interaction on percentage of heifers pubertal at beginning of breeding (P < 0.05) was 74.4 vs 76.3% in H-sired, 69.8 vs 60.5% in L-sired, and 76.2 vs 97.6% in P-sired heifers (LF vs HF, respectively). Number of AI services per pregnancy and final pregnancy percentage were not affected by diet or the diet x sire breed interaction. Diet affected progesterone (P < 0.05) and cholesterol (P < 0.001) concentrations, and sire breed tended to affect (P = 0.06) cholesterol concentrations. The effect of the diet x time on feed interaction on cholesterol concentrations was highly significant. There were no effects of diet or sample period on insulin or growth hormone concentrations in serially collected blood samples. We conclude that effects of supplemental dietary fat may be breed-dependent and hypothesize that a feeding period of approximately 60 d duration may be more appropriate than the 162 d used in this study.

Animal Feed↗

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.

Animal Feed↗

Effects of feeding beef females supplemental fat during gestation on cold tolerance in newborn calves.

Effects of prepartum fat supplementation of the dam on cold tolerance of calves were determined in two studies. In Exp. 1, 22 F1, crossbred heifers gestating F2 calves received diets containing either 1.7 or 4.7% dietary fat starting at d 230+/-2d of gestation. Safflower seeds (Carthamus tinctorius) containing 37% oil with 79% linoleic acid were the supplemental fat source in isocaloric-isonitrogenous diets. Calves were separated from their dams at birth, fed pooled dairy-cow colostrum, muzzled to prevent sucking, and returned to their dams in a heated (22 degrees C) barn for 3.5 h. At 4 h of age, a jugular catheter was inserted. At 5 h of age, calves were placed in a 0 degrees C room for 140 min and rectal temperatures and blood samples were obtained at 10- and 20-min intervals. Blood was assayed for glucose, cortisol, and cholesterol. In Exp. 2, 18 multiparous, crossbred beef cows bred to Murray Grey sires were randomly assigned to receive diets containing either 1.7 or 3.1% dietary fat starting at 235+/-2 d gestation. Safflower seeds were used as the supplemental fat source in isocaloric-isonitrogenous diets. At d 260 of gestation, premature parturition was induced in one-half of the cows from each diet group by feeding Ponderosa pine (Pinus ponderosa) needles. Experimental protocols were the same as in Exp. 1, except that cold exposure was at 9 degrees C for 200 min. Rectal temperatures were affected in Exp. 1 by time and diet x time (both P < .01) and diet x calf sex (P < .05) and in Exp. 2 by calf age (P < .05), time, and calf age x time (both P < .01). Plasma cortisol concentrations were affected by time (P < .01) and calf sex x time (P < .05) in Exp. 1 and by time ( P < .01) in Exp. 2. Cholesterol concentrations in Exp. 1 were affected by diet x time (P < .05) and in Exp. 2 by time (P < .05). Plasma glucose concentrations were affected in Exp. 1 by diet (P < .05) and in Exp. 2 by calf age, time, and calf age x time (all P < .01). We conclude from Exp. 1 that feeding heifers supplemental fat during late gestation increased glucose concentrations in the newborn calf, resulting in favorable responses in body temperature in the cold-stressed newborns. This increase in substrate availability suggests a potential positive effect on heat generation in newborns during sustained periods of cold stress. In Exp. 2, premature calves had compromised cold tolerance possibly due to impaired shivering or brown adipose tissue thermogenesis.

Adaptation, Physiological↗

Effects of prepartum supplementary fat and muscle hypertrophy genotype on cold tolerance in newborn calves.

Effects of feeding pregnant dams supplemental dietary fat during the last 55 d of gestation on cold tolerance of newborn crossbred calves with (Piedmontese cross, P, n = 15) or without (Hereford cross, H, n = 16) the muscle hypertrophy allele was determined. Primiparous F1 dams gestating F2 calves of the respective breeds were assigned randomly within breed to receive gestation diets containing either 2.2 (Low Fat; LF) or 5.1% fat (High Fat; HF). Safflower (Carthamus tinctorius L.) seeds containing 37% oil with 79% linoleic acid were the supplemental fat source in diets formulated to be isocaloric-isonitrogenous. At parturition, calves were separated from their dams, fed 38 degrees C pooled dairy cow colostrum (30 mL/kg BW), muzzled to prevent suckling, and returned to their dams in a heated (22 degrees C) room for 3.5 h. At 4 h of age (birth = 0 h), a catheter was inserted into the jugular vein. At 5 h of age, calves were placed in a 0 degrees C room for 140 min, and rectal temperatures and blood samples were obtained at 10- and 20-min intervals. Blood was assayed for cortisol and glucose. Rectal temperature was affected by diet (P<.05), time, diet x time, and breed x time (P<.01 for time and the interactions). Cortisol and glucose concentrations were not affected by diet, breed, or the diet x breed interaction, but they were affected by time, breed x time (both P<.01), and diet x time (P = .06). Calves from HF dams had higher rectal temperatures than calves from LF dams, and the HF calves maintained higher rectal temperatures throughout cold exposure. Cortisol concentrations were lower (P = .06) in calves from HF dams, and these calves had more (P = .06) glucose available for metabolic heat production than calves from LF dams. Piedmontese-cross calves maintained higher (P<.01) rectal temperatures and had higher cortisol and glucose (both P<.01) concentrations than did H-cross calves. We conclude that feeding dams supplemental fat during late gestation increased heat production in newborn calves and potentially could increase calf survival; calves with muscle hypertrophy may have a different ratio of shivering vs nonshivering thermogenesis due to differences in body composition or relationships among uncoupling proteins.

Adaptation, Physiological↗

Induced and synchronized estrus in cattle: dose titration of estradiol benzoate in peripubertal heifers and postpartum cows after treatment with an intravaginal progesterone-releasing insert and prostaglandin F2alpha.

Peripubertal beef heifers (n = 57) and postpartum multiparous cows (n = 52) were used to determine the optimal dose of estradiol benzoate (EB) to induce and synchronize estrus after treatment with intravaginal progesterone inserts (IVP4, EAZI-BREED CIDR). All females received an IVP4 for 7 d (d 0 = insertion day) with a 25-mg injection of PGF2alpha (Lutalyse) on d 6. At 24 to 30 h after IVP4 removal, females were randomly assigned to be injected subcutaneously with EB at the following doses: heifers 0, .2, .38, or .75 mg and cows 0, .25, .5, or 1 mg. Furthermore, seven heifers and seven cows from each dose group were bled every 4 h for 76 h starting at EB injection. Serum was collected and assayed for LH and estradiol-17beta (E2). Observations for signs of estrus were made twice daily for 21 d after removal of IVP4, and females were artificially inseminated 8 to 20 h after detection of estrus. The percentage of females showing estrous behavior was increased by EB (P < .04); the greatest response was at .38 mg in heifers (86%) and 1 mg in cows (100%). Dose x time interaction affected (P < .01) E2 concentrations in heifers and cows; the animals that received the higher doses of EB had greater E2 concentrations in a shorter time than those that received the smaller doses. The percentage of cows and heifers with an acute preovulatory LH release (peak LH) was affected by dose, with a linear (P < .01) and a quadratic (P < .01) response. Highest concentrations of LH during peak LH were affected by dose with a linear (P < .01) response in heifers and linear (P < .01) and quadratic (P < .08) responses in cows. Heifers receiving .38 mg and cows receiving .5 and 1 mg of EB had the highest peak LH. Time to LH peak had a linear (P < .03) response in heifers and had linear (P < .04) and quadratic (P < .05) responses in cows. Pregnancy rate was affected (P < .02) in heifers by whether or not they were anestrous before IVP4 treatment (those with estrous cycles = 52% vs those that were anestrous = 22%) and in cows by dose of EB (P < .01; 8, 23, 21, and 67% for 0, .25, .5, and 1 mg, respectively). In conclusion, in females treated with IVP4 and PGF2alpha to induce and synchronize estrus, an injection of EB increased concentrations of E2 and LH and increased number of animals showing estrus. Also, EB increased pregnancy rates in cows. Optimal responses were at .38 mg EB for heifers and at 1 mg EB for cows.

Administration, Intravaginal↗

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.

Animal Nutritional Physiological Phenomena↗

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.

Aging↗

Body temperature and endocrine interactions before and after calving in beef cows.

Multiparous beef cows (n = 7) were used to evaluate peripartum changes and interactions among body temperature (BT) and circulating progesterone (P4), estradiol-17beta (E2), triiodothyronine (T3), cortisol, thyroxine (T4), and 13,14-dihydro-15-keto-prostaglandin F2alpha (PGFM) concentrations. Electronic temperature monitors were placed under the obliquus abdominis internus muscle of the left flank, and BT was measured using radiotelemetry every 3 min for 10-s periods from 144 h before to 24 h after calving. Environmental temperatures (ET) were recorded hourly. Body and environmental temperatures were averaged, separately, within 8-h periods. Blood samples were collected every 8 h, and hormone concentrations were measured. Time of day affected BT (P < .01), at 0300 cows had the lowest BT, at 1900 the highest, and at 1100 values were intermediate. Body temperature remained relatively constant (P > .10) from 144 to 56 h before calving and from 8 to 24 h after calving but decreased (P < .01) from 48 to 8 h before calving. Precalving BT was affected (P < .01) by ET, but hour-before-calving (time) had the greatest effect on BT during the 48 to 8 h immediately preceding parturition (b' = .41, P < .01) and was independent of ET effects. Before the BT decrease, cows gestating heifers had lower (P < .01) BT than cows gestating bulls. Plasma E2, PGFM, T3, and T4 concentrations before the precalving decrease in body temperature were greater (P < .03) in cows gestating bull rather than heifer calves. Approximately 30% of the variation (R2) during the temperature decrease was explained by plasma hormone concentrations; PGFM (b' = -.30, P < .05) and T3 (b' = -.22, P < .10) had the most significant effects. In conclusion, BT of the cow before the precalving decrease was affected by ET and sex of calf. However, the prepartum BT decrease was independent of these variables, and seemed partially endocrine-induced.

Animals↗

Factors affecting dystocia in Brahman-cross heifers in subtropical southeastern United States.

This study was conducted to determine relative relationships among factors affecting dystocia in Brahman-cross heifers. Body and pelvic measurements were obtained in mid-June (when heifers were approximately 17 mo old), 45 d after a 60-d breeding season. Heifers studied were 207 Red Brangus, 209 Simbrah, and 250 Braford bred to Black Angus bulls; calving began on December 1. Heifers grazed stockpiled bahia and hemarthria grass or ryegrass supplemented with 0.9 kg of 32% protein cottonseed meal and 1.8 kg of mill-run black strap molasses daily during calving. Calvings were scored (1 = no difficulty to 4 = major difficulty). A random sample of birth weights were obtained on 131 and 210 calves in 1992 and 1993. Data were analyzed within year by SAS procedures. Breed differences in dam size and pelvic measurements were highly significant. Residual correlations between body weight and pelvic area were .20 and .35 (both P < .01) for 1991 and 1992. Dystocia incidence was 6.9% in 1992 and 10.5% in 1993, with higher incidence in males than in females (1992, 10.6 vs 3.1%, P = .08; 1993, 15.6 vs 4.2%, P < .01, male vs female, respectively). Male birth weight exceeded (P < .01) that of females (26.7 vs 24.3 kg, 1992; 28.1 vs 26.1 kg, 1993). Correlations among dam size and calf birth weight were not significant. Birth weight was significantly correlated with dystocia score (.19 and .49, 1992 and 1993). Path analyses of influences on dystocia found birth weight, dam heart girth, and body weight significant in 1992, but only birth weight significant in 1993. Regression of calving score on birth weight was curvilinear and significant in both years, with the birth weight inflection point at 22 kg. We conclude that dam body size data obtained following the breeding season were of minor value in determining dystocia, but birth weight was consistently important.

Animals↗

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.

Journal Article↗

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.

Animals↗

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.

Abortion, Veterinary↗

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)

Abortion, Veterinary↗

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)

Animals↗

Reproductive efficiency of range beef cows fed different quantities of ruminally undegradable protein before breeding.

Two studies, using 128 crossbred, multiparous beef cows grazing native winter and spring rangeland, were conducted to determine effects of protein supplementation on nutrient status and subsequent calf and reproductive performance. Postparturient cows (body condition score [BC] = 3.9) were fed 1.82 kg of one of two supplements (54% CP at 490 g of CP/d) per cow on alternate days. Supplements were formulated to contain 50% (245/490 g of CP) ruminally undegradable (UD) CP (RU50) or 25% (119/490 g of CP) UD CP (RU25) and were fed until breeding (BC = 4.2). Late-calving cows (Study 1) were individually fed supplement while grazing native range. Early-calving cows (Study 2) were group-fed supplement on alternate days while grazing native range and were daily fed approximately 5.4 kg of medium-quality grass hay (10.5% CP). Late-calving cows had similar (P > .22) BW losses postpartum, whereas early-calving cows fed RU50 lost 39 kg less (P < .01) BW than did cows fed RU25. Cows that received RU25 returned to estrus sooner (P < .02), in the late-calving study, than cows fed RU50 (47 vs 56 d, respectively). The percentage of cows serviced in the first 21 d of breeding (96 and 100% for late- and early-calving studies, respectively) and pregnancy rates (88 and 86% for late- and early-calving studies, respectively) did not differ regardless of postpartum protein supplement. When adequate CP was provided in the diet for optimum function of the rumen, addition of ruminally undegraded CP decreased weight loss of mature, postpartum beef cows grazing native range.(ABSTRACT TRUNCATED AT 250 WORDS)

Animal Feed↗

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)

Animals↗