Ovulation rate and twinning rate in cattle: heritabilities and genetic correlation

Repeated measures of ovulation rate on puberal heifers should be an effective way to select for increased twinning rate. A reliable estimate of the genetic correlation between ovulation and twinning rates is needed to implement such selection and to predict its efficiency. Restricted maximum likelihood was used to estimate genetic correlations from subsets of data collected from the twinning project at the Roman L. Hruska U.S. Meat Animal Research Center. The animal model included numerator relationships among the animals and fixed effects of year-season of measurement, age at measurement, and birth group. Genetic correlations between averages of ovulation rates for three, four, five, six, seven, and eight estrous cycles and the occurrence of twins were, respectively, .62, .76, 1.00, 1.00, 1.00, and .98 based on observations on 200 to 325 puberal heifers. Corresponding phenotypic correlations ranged from .06 to .26. Genetic correlations between ovulation rate in a single estrous cycle and occurrence of twins were .38, .98, and .98, respectively, for 323, 430, and 283 cows with ovulation rate measured after measurement of twinning, in the same season as measurement of twinning, and more than 1 yr before measurement of twinning. Phenotypic correlations were .00, .07, and .00. Genetic and phenotypic correlations among ovulation rates at six consecutive estrous cycles averaged, respectively, .66 and .12 for 610 heifers. Heritabilities for ovulation rates in individual cycles averaged .16. No evidence of negative environmental covariance between ovulation rates in adjacent cycles was found. These results support the approach of indirectly selecting for twinning rate by measuring ovulation rates in estrous cycles of puberal heifers.     

Genetic analysis of twinning rate and milk yield using a threshold‐linear model in Japanese Holsteins

The objective of this study was to estimate genetic parameters and breeding values for the twinning rate of the first three parities (T1, T2 and T3) and 305‐day milk yield in first lactation (MY), using a four‐trait threshold‐linear animal model in Japanese Holsteins. Data contained 1 323 946 cows calving between 1990 and 2007. Twinning was treated as a binary character: ‘single’ or ‘twin or more’. Reported T1, T2 and T3 were 0.70%, 2.87%, and 3.73%, respectively. Individual 305‐day milk yield was computed using a multiple trait prediction for cows with at least eight test‐day records. (Co)variance components were estimated via Gibbs sampling for randomly sampled subsets. Posterior means of heritabilities for T1, T2 and T3 were 0.11, 0.16 and 0.14, respectively. Genetic correlations between parities were 0.92 or greater. Genetic correlations of MY with twinning rate were not ‘significant’ (i.e. their 95% highest probability density intervals contained zeros). Multiple births at different parities were considered as the same genetic trait. The average evaluations of T1 (T2) for sires born before 1991 was 0.48% (2.25%) compared with a mean of 0.76% (3.37%) for sires born after 1992. A recent increase in the reported twinning rate reflects the positive genetic trend for sires in Japanese Holsteins.     

Twinning in cattle: II. Genetic and environmental effects on ovulation rate in puberal heifers and postpartum cows and the effects of ovulation rate on embryonic survival

The potential of ovulation rate before 18 to 21 mo of age in puberal heifers as an indirect selection criterion for twinning rate was considered. Heritability (h2) was .07 +/- .03 for single observations and .34 +/- .18 for the mean of 7.9 estrous cycles per heifer. Estimated repeatability (r) of ovulation rate was less than or equal to h2, indicating negligible permanent environmental effects. Expected h2 for mean ovulation rate (assuming h2 = r = .07 for single observations) for increasing numbers of estrous cycles would be as follows: 4, .23; 6., 31; 8, .38; and 10, .43. About 50% of the heifers produced no multiple ovulations, but 27% produced multiple ovulations in more than 15% of their estrous cycles. Ovulation rate varied seasonally and increased about .01 per month of age (P less than .05). Genetic correlation of mean ovulation rate with adjusted 368-d weight was low (.08 +/- .32). Ovulation rate in postpartum cows was higher (P less than .05) in fall than in spring (1.15 vs 1.08). In postpartum cows, estimated h2 = .24 +/- .13 and r = .17. Mean ovulation rate for postpartum cows was 1.12 vs 1.09 in puberal heifers, accounting in part for the higher h2. Pregnancy rate was higher (P less than .05) in multiple- than in single-ovulating cows. Effects of ovulation rate on embryonic survival were small (P greater than .05). Unilateral and bilateral multiple ovulations were not different in embryonic survival. Accuracy of ovulation rate determination by palpation per rectum was lower in multiple- than in single-ovulating postpartum cows, because some unilateral multiple corpora lutea, especially, were recorded as singles. Results suggest that use of ovulation rate in puberal heifers should permit effective indirect selection for twinning rate among yearling heifers based on individual performance and among young sires based on ovulation rate of sibs and daughters.     

Association of a single nucleotide polymorphism in SPP1 with growth traits and twinning in a cattle population selected for twinning rate

Continued validation of genetic markers for economically important traits is crucial to establishing marker-assisted selection as a tool in the cattle industry. The objective of the current study was to evaluate the association of a SNP (T(9)/T(10)) in the osteopontin gene (SPP1) with growth rate in a large cattle population spanning multiple generations and representing alleles from 12 founding breeds. This population has been maintained at the US Meat Animal Research Center since 1981 and subjected to selection for twinning rate. Phenotypic records for this population included twinning rate and ovulation rate, providing an opportunity to examine the potential effects of SPP1 genotype on reproductive traits. A set of 2,701 animals was geno-typed for the T(9)/T(10) polymorphism at SPP1. The geno-typic data, including previously genotyped markers on chromosome 6 (BTA6), were used in conjunction with pedigree information to estimate genotypic probabilities for all 14,714 animals with phenotypic records. The genotypic probabilities for females were used to calculate independent variables for regressions of additive, dominance, and imprinting effects. Genotypic regressions were fit as fixed effects in a mixed model analysis, in which each trait was analyzed in a 2-trait model where single births were treated as a separate trait from twin births. The association of the SPP1 marker with birth weight (P < 0.006), weaning weight (P < 0.007), and yearling weight (P < 0.003) was consistent with the previously reported effects of SPP1 genotype on yearling weight. Our data supports the conclusion that the SNP successfully tracks functional alleles affecting growth in cattle. The previously undetected effect of the SNP on birth and weaning weight suggests this particular SPP1 marker may explain a portion of the phenotypic variance explained by QTL for birth and HCW on BTA6.     

Evaluation of ovulation rate and ovarian phenotype in puberal heifers from a cattle population selected for increased ovulation rate

Long-term selection for increased ovulation rate (1984 to 2002) has resulted in a unique ovarian phenotype in the MARC Twinner cattle population. Ovulation rate and frequency of bilateral ovulations were examined by rectal palpation in 29,547 estrous cycles for 3,910 heifers (12 to 18 mo of age) in this population. Bilateral ovulations (one corpus lutuem [CL] on each ovary) were of interest because bilateral twin pregnancies result in decreased dystocia and increased calf survival. Ovulation rate increased linearly at a rate of 0.026 CL per year, and it currently averages 1.48 +/- 0.04 CL per estrous cycle. Concurrent with the increase in ovulation rate, the frequency of triplet ovulations increased from 0% to 2.3 +/- 0.8% (P < 0.001). Ovulation rate of both the right and left ovary increased equally at a rate of 0.013 CL per year, and mean ovulation rate of the right ovary remained greater than mean ovulation rate of the left ovary throughout the study (0.66 vs. 0.55 +/- 0.003 CL per estrous cycle; P < 0.001). Although correlations were low, ovulation rate of one ovary was negatively correlated (P < 0.001; r = -0.07) with ovulation rate of the same ovary in the previous estrous cycle, but positively correlated (P < 0.001; r = 0.13) with the contralateral ovary of the previous estrous cycle. The proportion of bilateral ovulations averaged 55.7 +/- 0.7%, a value greater than the predicted 49.5% (P < 0.001). In addition to dystocia and retained placenta, triplet pregnancies increase the incidence of pregnancies gestating fetuses of opposite sexes and subsequent incidence of freemartins; thus, selection pressure on ovulation rate may need to be adjusted in the MARC Twinner population. The proportion of bilateral ovulations in the population is greater than expected, and this may be an economically important trait, which will respond to selection and be beneficial for improving bovine reproductive efficiency. Understanding factors controlling the increased functional activity of the right ovary and bilateral ovulations may provide further insights into the mechanisms controlling follicle selection and methods to improve reproductive management of cattle.     

Confirmation of quantitative trait loci using a low-density single nucleotide polymorphism map for twinning and ovulation rate on bovine chromosome 5

Traditional genetic selection in cattle for traits with low heritability, such as reproduction, has had very little success. With the addition of DNA technologies to the genetic selection toolbox for livestock, the opportunity may exist to improve reproductive efficiency more rapidly in cattle. The US Meat Animal Research Center Production Efficiency Population has 9,186 twinning and 29,571 ovulation rate records for multiple generations of animals, but a significant number of these animals do not have tissue samples available for DNA genotyping. The objectives of this study were to confirm QTL for twinning and ovulation rate previously found on BTA5 and to evaluate the ability of GenoProb to predict genotypic information in a pedigree containing 16,035 animals when using genotypes for 24 SNP from 3 data sets containing 48, 724, or 2,900 animals. Marker data for 21 microsatellites on BTA5 with 297 to 3,395 animals per marker were used in conjunction with each data set of genotyped animals. Genotypic probabilities for females were used to calculate independent variables for regressions of additive, dominance, and imprinting effects. Genotypic regressions were fitted as fixed effects in a 2-trait mixed model analysis by using multiple-trait derivative-free REML. Each SNP was analyzed individually, followed by backward selection fitting all individually significant SNP simultaneously and then removing the least significant SNP until only significant SNP were left. Five significant SNP associations were detected for twinning rate and 3 were detected for ovulation rate. Two of these SNP, 1 for each trait, were significant for imprinting. Additional modeling of paternal and maternal allelic effects confirmed the initial results of imprinting done by contrasting heterozygotes. These results are supported by comparative mapping of mouse and human imprinted genes to this region of bovine chromosome 5.     

Multiple-trait restricted maximum likelihood for simulated measures of ovulation rate with underlying multivariate normal distributions.

A data set that was used to estimate covariance components with REML for an animal model with eight measures of ovulation rate treated as separate traits was used as a template to simulate data sets of eight multivariate normal traits that were then truncated to binomial traits. The model for simulation included eight measures on 610 animals with 1,071 animals in the numerator relationship matrix. Heritabilities were equal for the eight measures, and both genetic and phenotypic correlations among the measures were equal. Ten replications for each combination of heritability (.15, .25, and .35) and genetic correlation (.50, .66, and .90) were simulated on the normal scale. For each replicate, estimates of the eight heritabilities and 28 genetic correlations were obtained by multiple-trait REML. The usual transformation of heritability estimated on the binomial scale overestimated heritability on the normal scale. Genetic correlations on the binomial scale seriously underestimated the correlations on the normal scale. Standard errors of the estimates obtained by replication were somewhat larger than the approximate SE from REMLPK (the multi-trait REML program of K. Meyer). A final set of 10 simulated replications with heritability of .25 and genetic correlation of 1.00 resulted in average estimates of .18 for heritability and of .66 for genetic correlation that agree closely with those from the analysis of measures of ovulation at eight estrous cycles used as a template; averages for heritability of .16 and for genetic correlation of .66 were obtained.     

National cattle evaluation system for combined analysis of carcass characteristics and indicator traits recorded by using ultrasound in Angus cattle

The objectives were to 1) evaluate genetic relationships of sex-specific indicators of carcass merit obtained by using ultrasound with carcass traits of steers; 2) estimate genetic parameters needed to implement combined analyses of carcass and indicator traits to produce unified national cattle evaluations for LM area, subcutaneous fat depth (SQF), and marbling (MRB), with the ultimate goal of publishing only EPD for the carcass traits; and 3) compare resulting evaluations with previous ones. Four data sets were extracted from the records of the American Angus Association from 33,857 bulls, 33,737 heifers, and 1,805 steers that had measures of intramuscular fat content (IMF), LM area (uLMA), and SQF derived from interpretation of ultrasonic imagery, and BW recorded at the time of scanning. Also used were 38,296 records from steers with MRB, fat depth at the 12th to 13th rib interface (FD), carcass weight, and carcass LM area (cLMA) recorded on slaughter. (Co)variance components were estimated with ASREML by using the same models as used for national cattle evaluations by the American Angus Association. Heritability estimates for carcass measures were 0.45 +/- 0.03, 0.34 +/- 0.02, 0.40 +/- 0.02, and 0.33 +/- 0.02 for MRB, FD, carcass weight, and cLMA, respectively. Genetic correlations of carcass measures from steers with ultrasonic measures from bulls and heifers indicated sex-specific relationships for IMF (0.66 +/- 0.05 vs. 0.52 +/- 0.06) and uLMA (0.63 +/- 0.06 vs. 0.78 +/- 0.05), but not for BW at scanning (0.46 +/- 0.07 vs. 0.40 +/- 0.07) or SQF (0.53 +/- 0.06 vs. 0.55 +/- 0.06). For each trait, estimates of genetic correlations between bulls and heifers measured by using ultrasound were greater than 0.8. Prototype national cattle evaluations were conducted by using the estimated genetic parameters, resulting in some reranking of sires relative to previous analyses. Rank correlations of high-impact sires were 0.91 and 0.84 for the joint analysis of MRB and IMF with previous separate analyses of MRB and IMF, respectively. Corresponding results for FD and SQF were 0.90 and 0.90, and for cLMA and uLMA were 0.79 and 0.89. The unified national cattle evaluation for carcass traits using measurements from slaughtered animals and ultrasonic imagery of seed stock in a combined analysis appropriately weights information from these sources and provides breeders estimates of genetic merit consistent with traits in their breeding objectives on which to base selection decisions.     

Effects of ovulation rate and fetal number on fertility in twin-producing cattle

Effects of ovulation rate and of fetal number and distribution within the uterus on pregnancy rate and fetal survival were evaluated in nulliparous (n = 1,331) and parous (n = 3,517) cattle selected for twinning. Cattle were divided into a spring (70 d) and fall (60 d) breeding season and bred by a combination of AI and natural service. Ovulation rate, pregnancy status, and fetal number and distribution were determined by transrectal, real-time ultrasonography of the uterus and both ovaries at the end of the breeding season. Pregnancy was reconfirmed by rectal palpation at 75 to 135 d of gestation. For heifers and cows combined, ovulation rate increased (P < 0.01) from 1.46 +/- 0.4 in 1994 to 1.89 +/- 0.4 in 2004; number of calves per parturition increased (P < 0.01) from 1.34 +/- 0.3 to 1.56 +/- 0.3, respectively, which included an increase in triplet and quadruplet ovulations and triplet births. Bilateral twin ovulations yielded proportionately more (P < 0.01) twin births than unilateral twin ovulations. Ovulation rate was greater (P < 0.01) in the fall than spring breeding season. Pregnancy rate at ultrasound diagnosis did not differ among females with 1, 2, or 3 ovulations (89.1 +/- 0.7, 91.2 +/- 0.7, or 91.5 +/- 2.8%, respectively), but rates at calving decreased (P < 0.01) with increasing ovulation rate (85.1 +/- 0.6, 82.7 +/- 0.6, or 64.2 +/- 2.7%, respectively). Pregnancy rate was less (P < 0.01) after twin or triplet births than single births. For dams birthing twins or triplets, pregnancy rate was less in the fall vs. spring, but rates were similar between seasons for dams with a single birth (type of birth x season, P < 0.05). Cows 60 d, regardless of type of birth. Maintenance of pregnancy to term differed (P < 0.01) among females diagnosed with 1, 2, or 3 fetuses (95.7 +/- 0.6, 87.8 +/- 0.8, and 54.9 +/- 2.3%, respectively). The reduced survival of twin and triplet fetuses in heifers had occurred (P < 0.01) by d 75 to 135 of gestation, and fetal losses were greater (P < 0.01) for unilateral than bilateral twins or triplets, whereas loss of twin or triplet fetuses in cows occurred later in gestation, and losses were not affected by uterine location. Thus, increased calf production from selecting for increased ovulation rate in beef cattle is tempered by increased fetal mortality, partially associated with the crowding of 2 or 3 fetuses within 1 uterine horn, especially in heifers.     

Ovarian follicular dynamics and hormones throughout the estrous cycle in Thai native (Bos indicus) heifers

Relatively few studies have been reported regarding the reproductive physiology of female Thai native cattle. Therefore, the objective of the present study was to evaluate the follicular dynamics and concentrations of follicle stimulating hormone (FSH), estradiol (E2) and progesterone (P4) during the estrous cycle in Thai native heifers (TNH) and to compare obtained results with those of European and Indian cattle breeds previously reported. For the detection of estrus, ovaries of all 20 heifers were examined twice daily (12 h intervals) by ultrasonography for three consecutive estrous cycles. From data of 60 estrous cycles (n = 60 estrous cycles from 20 heifers), it was found that 14 (70%) and 6 heifers (30%) had two (42 estrous cycles collected from 14 heifers) and three follicular waves (18 estrous cycles collected from 6 heifers), respectively. The days when estrus was detected, interovulatory intervals, life‐spans of corpus lutea (CL), and days for growing and regression of CLs were shorter in the two follicular waves than those in the three follicular waves (P < 0.05). In both two and thre follicular waves, larger maximum diameters and higher growth rates of the dominant follicle (DF) in an ovulatory wave were observed than those of the preceding waves without ovulation (P < 0.05). There was a progressive increase in follicular size and FSH and E2 production during follicular growth in each follicular wave. In addition, the FSH and E2 peak concentrations during the ovulatory wave were higher than those of the anovulation waves (P < 0.05). Moreover, although the ovarian follicular dynamic patterns in Thai native heifers were similar to those previously reported for European and Indian cattle breeds, the diameter of the largest preovulatory follicle (OF), subordinate follicles (SF) and CLs were smaller than those in European and Indian cattle breeds. In conclusion, when compared with European and some breeds of Indian cattle, the length of interovulatory intervals was shorter, and the sizes of dominant SF and CLs were smaller in Thai native heifers.     

Relationship between pharmacological induction of estrous and/or ovulation and twin pregnancy in the Thoroughbred mares

The aim of this study was to evaluate the possible relationship of pharmacological induction of estrous and/or ovulation with the occurrence of twin pregnancies in Thoroughbred mares. Out of 680 mares, 356 received one of the following treatments during the estrous cycle in which they became pregnant: injection of 0.5mg of cloprostenol at the ultrasonographic detection of a CL (n=86); injection of 5000 IU human chorionic gonadotropin (hCG) immediately before mating (n=221); injection of 0.5mg of cloprostenol at the ultrasonographic detection of a CL plus injection of 5000 IU hCG immediately before mating on cloprostenol-induced estrous (n=49). The other 324 mares, not treated for induction of estrous or ovulation in the estrous cycle resulting in pregnancy, were used as control group. The occurrence of twin and single pregnancies in treated and control mares underlines that the percentage of twin pregnancy in treated mares (16.6%) was statistically significantly higher (P<0.0001; odds ratio, OR=2.87) than the percentage of twinning in the control group (6.5%). Comparison of the occurrence of twins between treatments revealed a statistically significant difference between mares treated with hCG alone compared to animals given prostaglandin F2alpha (PGF2alpha) plus hCG. The results show a statistically significant difference for each treatment compared to controls, with the least difference (P<0.05; OR=2.18) for the comparison between hCG treatment group and controls, a significance of P<0.01; OR=3.05 for the comparison between PGF2alpha treatment and controls, and a highly statistically significant difference (P<0.0001; OR=6.37) for the comparison between PGF2alpha plus hCG-treated animals and controls.     

Twinning in Dairy Cattle

Twinning in dairy cattle is an unavoidable outcome of reproduction and is undesirable because it reduces the overall profitability of a dairy operation through negative effects on cows calving twins as well as on calves born as twins. Cows calving twins are at greater risk for many periparturient reproductive and metabolic disorders than nontwinning herdmates, and incidences of abortion, stillbirth, neonatal calf mortality, and reduced birth weight are greater among twin compared with singleton calves. Twinning is a complex trait with multiple causative factors, and empirical evidence supports a role for both genetic and environmental risk factors in cattle. Risk factors for twinning include genetics, season, parity, ovulation rate, and milk production. The observation that twinning has increased in the dairy cattle population over time suggests a concurrent change in one or more of these causative factors during this same period. At present, dairy farmers and their consultants are ill prepared to make sound-management decisions to mitigate the negative effects of twinning on their operations because of a lack of applied scientific data on management strategies for periparturient dairy cows carrying twin fetuses. A clear understanding of the factors responsible for twinning is essential for future development of strategies to manage twinning in dairy operations.     

THE DURATION OF OESTRUS AND THE TIME OF OVULATION IN CATTLE OF THREE BREED TYPES WITH AND WITHOUT SYNCHRONISATION OF OESTRUS WITH A PROGESTOGEN

The duration of oestrus and the interval from onset of oestrus to ovulation has been studied in heifers of Brahman x Shorthorn, Hereford, Shorthorn and mixed dairy breeds following treatment with synthetic progesterone (CAP) and during a subsequent cycle. The animals were under observation for 24 hr a day. No significant differences were observed between breeds in either the length of oestrus or the interval to ovulation; nor could a difference be shown within breeds due to treatment with CAP. The mean duration of oestrus was 13.9 ± 0.5 (SE) hr, and the mean interval from onset of oestrus to ovulation was 26.9 ± 0.6 (SE) hr.     

Selection for ovulation rate in rabbits: genetic parameters, direct response, and correlated response on litter size

The aim of this work was to evaluate the response to 10 generations of selection for ovulation rate. Selection was based on the phenotypic value of ovulation rate, estimated at d 12 of the second gestation by laparoscopy. Selection pressure was approximately 30%. Line size was approximately 20 males and 80 females per generation. Traits recorded were ovulation rate at the second gestation, estimated by laparoscopy as the number of corpora lutea in both ovaries; ovulation rate at the last gestation, estimated postmortem; ovulation rate, analyzed as a single trait including ovulation rate at the second gestation and ovulation rate at the last gestation; right and left ovulation rates; ovulatory difference, estimated as the difference between the right and left ovulation rates; litter size, estimated as the total number of kits born and the number of kits born alive, both recorded at each parity. Totals of 1,477 and 3,031 records from 900 females were used to analyze ovulation rate and litter size, respectively, whereas 1,471 records were used to analyze ovulatory difference, right ovulation rate, and left ovulation rate. Data were analyzed using Bayesian methodology. Heritabilities of ovulation rate, litter size, number of kits born alive, right ovulation rate, left ovulation rate, and ovulatory difference were 0.16, 0.09, 0.08, 0.09, 0.04 and 0.03, respectively. Phenotypic correlations of ovulation rate with litter size, number of kits born alive, and ovulatory difference were 0.09, 0.01, and 0.14, respectively. Genetic correlations of ovulation rate with litter size and with number of kits born alive were estimated with low accuracy, and there was not much evidence for the sign of the correlation. The genetic correlation between ovulation rate and ovulatory difference was positive (P = 0.91). In 10 generations of selection, ovulation rate increased in 1.32 oocytes, with most of the response taking place in the right ovary (1.06 oocytes), but there was no correlated response on litter size (-0.15 kits). In summary, the direct response to selection for ovulation rate was relevant, but it did not modify litter size because of an increase in prenatal mortality.     

Twinning in cattle: I. Foundation animals and genetic and environmental effects on twinning rate

Foundation cows were selected using prior records from one of two sources, private herds or other projects at the Research Center. Comparing twinning rates before and after selection, the repeatability was lower for those from the first (.08) than for those from the second (.16) source with a combined value of .12. Realized heritability of single-parity twinning rate estimated from selection of parents and response in daughters of foundation females was .06. Paternal half-sib estimate of heritability of twinning rate was .02 +/- .07. Estimates of repeatability computed from calving records of females born in the project indicate that permanent environmental effects on twinning rate in cattle are small. Mean calving rate of females born in the project was 1.11 in the data set that included all data and 1.09 in the data set that excluded females from highly selected parents. Twinning rate was greater (P less than .05) in fall than in spring calving (1.13 vs 1.06). Data on twinning rate of a sample of the Swedish Friesian breed were summarized. Mean twinning rate of the Swedish Friesian breed is 2.57%. Age adjusted mean twinning rate of daughters of 32 half-sib sons of one particular Swedish Frieisan sire averaged 5.4% and ranged from .9% to 13.6%. There was no indication of a bimodal distribution, which would be expected if a single gene with a major effect on twinning rate were segregating. The estimated genetic standard deviation (sigma-xn) for mean twinning rates of the 32 sire progeny groups was 1.8%. Observed range among son progenies was .127 or 7.2 sigma-xn, in reasonable agreement with the hypothesis that twinning rate in this population is inherited as a quantitative trait.     

The effect of twinning on milk yield,dystocia, calf birth weight and open days in Holstein dairy cows of Iran

Calving records of Iranian Holsteins from April 1998 to September 2006 comprising 16 herds with 104 572 calving events representing 4045 twin births were used to evaluate reported open days, calving difficulties and calf birth weight in single‐ and twin‐births and the relationship exists between twinning and milk production. A logistic regression model was constructed to analyse dystocia for single‐ and twin‐births. In addition, statistical analyses of 305‐day milk yield, open days and calf birth weight were performed using the general linear models procedure. The odds of dystocia was greater after twin births [p < 0.0001; odds ratio (OR) = 2.32]. The odds of dystocia decreased from parity 1 to parity 2 and beyond (p < 0.0001; OR = 0.44). Open days were significantly different between single (129.28 days) and twin (144.88 days) births (p < 0.05). Calf birth weights were significantly greater for singletons than twins (43.33 kg vs. 34.36 kg; p < 0.05). In addition, twin‐calved cows had greater 305‐day milk production than single‐calved cows (p < 0.05). In general, development of practical management strategies to cope with the negative effects associated with twinning on dairies is critical, especially if the trend towards increased twinning in the dairy cattle population continues.     

National genetic improvement programs for dairy cattle in the United States

Rate of genetic improvement for milk yield has been increasing in recent years. Cows born in 1986 were about 135 kg superior in breeding value for milk yield to those born in 1985. Over 2.2 million cows contribute new data to genetic evaluations for production traits annually. These evaluations are computed with an animal model that provides best linear unbiased predictions of transmitting abilities for milk, fat, and protein yields and fat and protein percentages. The model includes effects of management group, permanent environment, herd-sire interaction, and animal genetic merit. Unknown-parent groups represent the genetic merit of base populations defined by birth year and sex. Type appraisal data are collected by breed associations and are evaluated with a sire model. Holstein cow evaluations are computed using scores from all appraisals and a multitrait model; evaluations for other breeds are computed using all appraisal scores, a repeatability model, and a single-trait system. Dystocia data are collected by individual AI organizations and dairy records processing centers; they are analyzed by a categorical-trait sire model at Iowa State University with support from the National Association of Animal Breeders. The AI organizations have been extremely important in increasing rate of genetic progress by increasing numbers of young bulls sampled, increasing selection intensity of bull dams through multiple ovulation and embryo transfer, and shortening generation interval through the use of younger cows and some virgin heifers as bull dams. (ABSTRACT TRUNCATED AT 250 WORDS)     

Pregnancy rate and first-service conception rate in Angus heifers

The objective of this project was to determine the genetic control of conception rate, or pregnancy percentage in Angus beef heifers. Producers from 6 herds in 5 states provided 3,144 heifer records that included breeding dates, breeding contemporary groups, service sires, and pregnancy check information. Two hundred fourteen sires of the heifers were represented; with 104 sires having less than 5 progeny, and 14 sires having greater than 50 progeny. These data were combined with performance and pedigree information, including actual and adjusted birth weights, weaning weights, and yearling weights, from the American Angus Association database. Heifer pregnancy rate varied from 75 to 95% between herds, and from 65 to 100% between sires, with an overall pregnancy rate of 93%, measured as the percentage of heifers pregnant at pregnancy check after the breeding season. Pregnancy was analyzed as a threshold trait with an underlying continuous distribution. A generalized linear animal model, using a relationship matrix, was fitted. This model included the fixed effects of contemporary group, age of dam, and first AI service sire, and the covariates of heifer age at the beginning of breeding, adjusted birth weight, adjusted weaning weight, and adjusted yearling weight. The relationship matrix included 4 generations of pedigree. The heritability of pregnancy and first-service conception rates on the underlying scale was 0.13 +/- 0.07 and 0.03 +/- 0.03, respectively. Estimated breeding values for pregnancy rate on the observed scale ranged from -0.02 to 0.05 for sires of heifers. Including growth traits with pregnancy rate as 2-trait analyses did not change the heritability of pregnancy rate. As expected for a reproductive trait, the heritability of pregnancy rate was low. Because of its low heritability, genetic improvement in fertility by selection on heifer pregnancy rate would be expected to be slow.     

Photoperiod influences age at puberty of heifers

Two experiments were conducted to determine if exposure of prepubertal heifers to supplemental lighting hastens the onset of puberty. In Exp. 1, 16 heifers were paired according to birth date (April 21 to July 4) and assigned randomly to exposure to either 18 h light/d (L) or natural photoperiods (N) from 22 wk of age until puberty. Twenty-two heifers in Exp. 2, born between February 27 and March 31 and between May 3 and May 17, 1981, were exposed to L or N from 24 wk of age until March 23, 1982. In Exp. 2, animals were bred at all estrous periods until conception. Age at first ovulation and first estrus were less (P less than .01 for Exp. 1 and P less than .10 for Exp. 2) for L than N heifers. Average ages at first estrus were 318 (L) and 367 d (N) for Exp. 1 and 367 (L) and 394 d (N) for Exp. 2. Age at conception in Exp. 2 was similar for L (380 d) and N (396 d) groups. There were no significant differences between L and N heifers in changes in body weight for either experiment. There was a photoperiod X age interaction (P less than .06) for ovarian volume in Exp. 1 because the rate of ovarian growth was greater for L than N heifers. Concentrations of LH were not affected by photoperiod in Exp. 1 and not measured in Exp. 2. There were no significant changes in LH concentrations between 22 and 34 wk of age. When expressed relative to first ovulation, LH levels were highest at 7 and 2 wk before first ovulation. Concentrations of prolactin in Exp. 1 were not significantly affected by photoperiod. It was concluded that supplemental lighting after 22 or 24 wk of age reduced ages at first ovulation and first estrus in heifers born from February to July. These effects of photoperiod were accompanied by changes in ovarian development.