The effect of season on the ovulation rates of Merino and crossbreed ewes in Western Australia

1969 ◽  
Vol 9 (38) ◽  
pp. 267 ◽  
Author(s):  
HE Fels ◽  
HG Neil ◽  
IG Ralph ◽  
RJ Suiter

Five experiments involving Merino and Border Leicester X Merino crossbred ewes were carried out to investigate the effect of season on ovulation and ovulation rate in the Western Australian agricultural areas. In one experiment, involving Murray Merinos only, effects of body weight and of introduction of teaser rams were also investigated. In 1966 the breeding season began in January for Murray Merinos, but in 1966-67 some ewes had already ovulated in December. Introduction of teaser rams in early December made teased ewes ovulate sooner than unteased ewes. The number of ovulations per ewe ovulating increased during the breeding season, reaching peaks of 1.8 eggs per ewe ovulating in April and early May 1966, and 1.6 eggs per ewe ovulating in February 1967. Supplementary feeding hastened the onset of the breeding season and tended to increase ovulation rate. Peppin Merinos showed a low incidence of ovulation, which was ascribed to their very poor body condition. The Border Leicester X Merino crossbred ewes began their breeding season in March in one experiment, but more than half the ewes had already ovulated in December in the other experiment, perhaps because they were much heavier. Both group's showed marked increases in ovulation rate as their breeding seasons progressed.

1901 ◽  
Vol 35 (6) ◽  
pp. 458-479
Author(s):  
M. Beeton ◽  
G. U. Yule ◽  
Karl Pearson

According to the Darwinian theory of evolution the members of a community less fitted to their environment are removed by death. But this process of natural selection would not permanently modify a race, if the members thus removed were able before death to propagate their species in average numbers. It then becomes an important question to ascertain how far duration of life is related to fertility. In the case of many insects death can interfere only with their single chance of offspring; they live or not for their one breeding season only. A similar statement holds good with regard to annual and biennial plants. In such cases there might still be a correlation between duration of life and fertility, but it would be of the indirect character, which we actually find in the case of men and women living beyond sixty years of age—a long life means better physique and better physique increased fertility. On the other hand, there is a direct correlation of fertility and duration of life in the case of those animals which generally survive a number of breeding seasons, and it is this correlation which we had at first in view when investigating the influence of duration of life on fertility in man. The discovery of the indirect factor in the correlation referred to above was therefore a point of much interest. For it seems to show that the physique fittest to survive is really the physique which is in itself (and independently of the duration of life) most fecund.


1977 ◽  
Vol 24 (3) ◽  
pp. 377-385 ◽  
Author(s):  
M. J. Ducker ◽  
J. S. Boyd

SUMMARYBody size was estimated for 255 Greyface ewes using five linear body dimensions. On the basis of this calculated measure combined with a subjective measure of body size 50 small and 50 large ewes were selected for use in the experiment. Precise ovulation data were obtained by endoscopy and this technique allowed the ewes to be mated subsequently.Body size did not affect the mean ovulation rate of the ewes although, at the same level of body condition, the large ewes were 25% heavier than the small ewes. The ovulation rates and the numbers of lambs born were influenced by changes in live weight and body condition. For these reasons live weight per se was not a good indicator of ovulation rate as ewe live weight was a combination of both body size and body condition. At the same live weight small ewes in improving body condition had a significantly higher ovulation rate than large ewes in reducing body condition.The onset of the breeding season of the ewes was not affected by their body size. The mean date of onset of oestrous activity for both large and small ewes was 17 October 1972 at a latitude 55° 52′ N.


1972 ◽  
Vol 78 (2) ◽  
pp. 245-249 ◽  
Author(s):  
J. C. Guerra ◽  
C. J. Thwaites ◽  
T. N. Edey

SUMMARYGroups of mature Merino ewes selected on the basis of either large or small bodysize were differentially fed during a pre-experimental period to produce subgroups of high and low body condition. These levels of body condition were maintained for 2 weeks before mating and for the first 5 weeks of gestation. Thereafter, the four subgroups grazed together until lambing.Big ewes had more multiple ovulations than small ewes (14/41 υ 6/53; P < 0·01), and there was a significant linear regression of ovulation rate on body size. Body condition was positively related to the incidence of multiple ovulations, but the regression of ovulation rate on body condition at mating failed to reach significance. Body weight was significantly related to both ovulation rate and the incidence of multiple ovulations, and proved to be a more effective predictor of ovulation rate than either body size or condition.These results make it clear that size and condition, the two components of body weight, each have a considerable independent influence on some aspects of reproduction, and that the precision of some experiments and the effectiveness of some production routines could be improved by considering them separately.


Author(s):  
L. Zarazaga ◽  
F. Forcada ◽  
J.A. Abecia ◽  
J. Mozota

Induction of oestrus and pregnancy in the seasonal anoestrus permits lambing during the breeding season and mating in a short period of time after weaning, but after spring lambing postpartum anoestrus is longer than it is in autumn lambing, and no breeds are able to resume cyclic activity two months after lambing. Nutrient status has been shown to be a major factor affecting the onset of ovarian cyclicity in postpartum ewes. On the other hand, melatonin implants were demonstrated to be efficient in advancing the annual breeding season, but the efficiency of this treatment could be modified by the nutritional status of the animals. The aim of this experiment was to determine the effect of exogenous melatonin, connected with the plane of nutrition after weaning, on the resumption of sexual activity and ovulation rate (OR) in a synthetic Spanish sheep breed lambing in spring.


1979 ◽  
Vol 28 (2) ◽  
pp. 245-255 ◽  
Author(s):  
P. A. Geisler ◽  
J. S. Fenlon

ABSTRACTAn analysis of the records of ewe weight and condition at mating together with subsequent lambing performance for several commercial flocks in the UK revealed no significant relationship between lambing performance and size, measured by weight transformed to a standard condition. The relationship between mating weight and body condition score at mating was linear though there was considerable variation in weight at a fixed body condition, suggesting a substantial spread in skeletal size. Increases in ovulation rate were not discernible from lambing figures over the range of body conditions observed in these flocks.


1989 ◽  
Vol 120 (1) ◽  
pp. 59-65 ◽  
Author(s):  
J. K. Findlay ◽  
B. Doughton ◽  
D. M. Robertson ◽  
R. G. Forage

ABSTRACT Immunization of ewes against a pure recombinant preparation of the α subunit of bovine inhibin (α-bI) resulted in a three- to fourfold increase in ovulation rate, associated with antibodies in plasma recognizing pure native 31 kDa inhibin. The aim of this study was to examine the effects of this immunization on basal and GnRH-stimulated plasma concentrations of FSH and LH in ewes during the anoestrous and breeding seasons. The groups were untreated control ewes (n = 5), control ewes treated with keyhole limpet haemocyanin (KLH alone, n = 4), ewes treated with α-bI alone (n = 4) and α-bI–KLH conjugate-treated ewes (n = 3). There were no effects of immunization on basal FSH or LH in anoestrous ewes, despite the presence of antibodies recognizing 31 kDa inhibin. In the breeding season, immunization against α-bI resulted in increased basal (follicular phase, P < 0·1; luteal phase P < 0·05) and GnRH-stimulated (follicular phase only, P < 0·001) release of FSH, but not LH. The data are compatible with the hypotheses that the increase in ovulation rate in immunized ewes is due to an increase in circulating FSH concentrations and that inhibin may only have a major peripheral influence on FSH in sheep during the breeding season. Journal of Endocrinology (1989) 120, 59–65


2016 ◽  
Vol 72 (12) ◽  
pp. 755-759 ◽  
Author(s):  
Monika Bryl ◽  
Hanna Bis-Wencel ◽  
Brygida Ślaska ◽  
Bożena Nowakowicz-Dębek ◽  
Zbigniew Bełkot ◽  
...  

The aim of this study was to assess the impact of the leptin concentration and body weight of mink females on the birth parameters of their kits. Blood samples were collected 3 times during preparation for reproduction, 7±2 days before mating. Total leptin concentration in serum was measured using commercial RIA kits (Millipore, St. Charles, Missouri USA). Research was conducted on 20 clinically healthy scanbrown female minks (Neovison Vison) aged 2-3 years. To evaluate their body condition, the females were divided into two groups based on the BCS scoring system. In the first group, referred to as BCS 2, lean females were included, and the second group (BCS 4) consisted of obese females. In mink dams belonging to BCS 2, the average leptin values were one-fourth of those in the BCS 4 group. The results obtained indicate the influence of the body mass of minks during preparation for reproduction on serum leptin concentration. The results of the Mann-Whitney U test showed a statistically significant difference between weights and leptin concentrations in groups BCS 2 and BCS 4. Among the other traits, such differences were not found. The analysis of results obtained in the two mink groups did not reveal a clear relationship between leptin in the serum of mothers before mating and the birth parameters of their kits.


2018 ◽  
Vol 46 (1) ◽  
pp. 8 ◽  
Author(s):  
André Luis Mallmann ◽  
Gabriela Da Silva Oliveira ◽  
José Zacarias Rampi ◽  
Felipe Basquera Betiolo ◽  
Deivison Pereira Fagundes ◽  
...  

Background: Body condition score is used widely in swine production to ensure adequate nutritional levels in sows during gestation and lactation. However, body condition score is not a gold standard for the estimation of nutritional requirements in sows. Post-farrowing sow body weight assessment might serve as a useful approach for the better adjustment of the nutritional requirements during lactation; however, this approach is time-consuming, requires labor, and might result in detrimental effects on the sow behavior and welfare. The objective of the present study, therefore, was to formulate prediction equations for the estimation of post-farrowing sow weight.Materials, Methods & Results: Seven equations were formulated for predicting the post-farrowing sow body weight, by using the data from three databases, which comprised a total 522 sows (434 gilts and 88 multiparous). The sows were weighed on Day 112 of gestation and after farrowing within 12 h. The piglets birth weight was recorded within 24 h after farrowing. The equations were formulated considering all the parity orders. While formulating the equations, the following five variables were used: pre-farrowing body weight, piglets born, litter weight, the interval between pre-farrowing weighing and farrowing (in days), and the total feed intake between pre-farrowing and post-farrowing weighing. The seven models were compared using the sets of possible predictors through regression with the best subsets procedure (Minitab for Windows, v. 18). Equations (EQ) 1, 2, and 4 were validated with a database comprising 732 sows (parity orders: 1–5). The females were weighed on Day 107 of gestation and within 24 h after farrowing. The predicted weights estimated by EQ 2 and 4 (215.4 ± 34.3 kg and 216.7 ± 34.4 kg, respectively) did not significantly differ from the observed weight (216.8 ± 34.6 kg) [P > 0.05].Discussion: Pre-farrowing sow body weight was identified as the main input variable required for the estimation of the post-farrowing sow body weight. Thus, even EQ 1, which contained only this variable, exhibited a high coefficient of determination (R2 = 0.8707). However, the R2 value kept increasing as more input variables were included in the equation. Equation 2, 4, and 6 included the litter weight variable, and the addition of this variable increased the numerical value of R2 from 0.8707 in EQ 1 to 0.8975 in EQ 2. The EQ 3, 5, and 7 considered the piglets born variable as well, which increased the R2 value from 0.8707 in EQ 1 to 0.9119 in EQ 3. The coefficient of determination did not vary much among the equations; therefore, the selection of the prediction equations depended on data availability, feed management, facility, and the reliability of data collection in each farm. Although EQ 1 demonstrated a greater correlation between the predicted and the observed post-farrowing weight compared to the other equations, the values of error in central tendency and the errors due to disturbances were numerically higher for EQ 1 in comparison to the other two equations (EQ 2 and 4). Therefore, it is suggested that EQ 1 should be used as the last choice for the estimation of post-farrowing sow weight as it presented low trueness and precision, and also because the predicted weight estimated by EQ 1 was statistically lower than the observed weight (211.67 ± 33.33 kg vs. 216.84 ± 34.62 kg; P = 0.012). EQ 4 emonstrated higher trueness and precision; however, it did not differ significantly from EQ 2 and 1. Further analyses are required in order to validate EQ 3, 5, 6, and 7. Among the equations that were predicted as well as validated, the simplest and the easiest equation with satisfactory results for trueness and precision was EQ 2, which is as follows:Post-farrowing sow weight (kg) = 13.03 + (0.93 × pre-farrowing body weight, kg) + (–1.23 × piglets born, n)


1969 ◽  
Vol 11 (4) ◽  
pp. 505-510 ◽  
Author(s):  
B. Hardy ◽  
G. A. Lodge

SUMMARYTwenty-four sows from three nutritional regimes imposed until weaning of their third litters were used to investigate the influence of weight and body condition on ovulation rate.For low-, medium- and high-plane sows respectively, mean corpora lutea numbers at 3 to 6 days post coitus were 13·8±0·78, 16·4±0·87 and 15·2±1·01 (not significantly different); conception rates at first service were 50, 87·5 and 100% percentages prenatal mortality were 36·1±7·95, 67·2±7·26 and 41·7±7·26, and mean numbers of pigs born alive were 9·0±1·19, 5·2±1·09 and 8·8±1·09.Pooled data indicated no significant effect of body weight but a significant effect of weight loss during the preceding lactation on ovulation rate (P<0–01).


2009 ◽  
Vol 114 (1-3) ◽  
pp. 175-182 ◽  
Author(s):  
M.A. De Santiago-Miramontes ◽  
B. Malpaux ◽  
J.A. Delgadillo

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