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Digitalcommons@University of Nebraska - Lincoln Digitalcommons@University of Nebraska - Lincoln
Digitalcommons@University of Nebraska - Lincoln Digitalcommons@University of Nebraska - Lincoln
June 1973
I. T. Omtvedt
USDA, iomtvedt1@unl.edu
Johnson, R. K. and Omtvedt, I. T., "EVALUATION OF PUREBREDS AND TWO-BREED CROSSES IN SWINE:
REPRODUCTIVE PERFORMANCE" (1973). Faculty Papers and Publications in Animal Science. 76.
https://digitalcommons.unl.edu/animalscifacpub/76
This Article is brought to you for free and open access by the Animal Science Department at
DigitalCommons@University of Nebraska - Lincoln. It has been accepted for inclusion in Faculty Papers and
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EVALUATION OF PUREBREDS AND TWO-BREED CROSSES IN
SWINE: REPRODUCTIVE PERFORMANCE 1
1279
J O U R N A L O F A N I M A L S C I E N C E , vol. 37, no. 6, 19"/3
1280 JOHNSON AND OMTVEDT
1967; Smith and McLaren, 1967). However, all three gilts of each breed. One of the three gilts
of these studies were consistent in reporting of each breed mated to each boar was randomly
increased survival rates for the crossbred pigs. designated to be slaughtered 30-days postbreed-
Lush et al. (1939) suggested that breeds may ing and the reproductive tract evaluated for
differ in their response to crossing. Craft (1953) early embryo development. This procedure was
and Bradford, Chapman and Grummer (1958) followed in making matings for the spring 1971
have shown that the comparison of inbred lines farrowing season, in which slaughter and farrow
for litter traits was of little value in predicting information is included on 45 and 89 gilts,
the performance of a line as a dam line in respectively. In order to increase the numbers
crossing. Since there is little information avail- available for evaluating early embryo develop-
able involving crossbreeding with the modern- ment, about half of the gilts that farrowed in
day breeds of swine raised under confinement spring 1971 were randomly selected to produce
management systems, data on the purebred a second litter in fall 1971. Approximately the
performance and combining ability are needed same number of gilts as the previous season
in order to develop breeding programs that will were also mated. A new group of boars of each
yield maximum performance. breed was used and the matings were made in
This paper provides information concerning the manner described above. In this season,
the reproductive performance of purebred Du- each boar was mated to at least two gilts and
roc, Hampshire and Yorkshire females when one sow of each breed. All of the sows and
producing purebred and crossbred litters. Pro- enough gilts to produce 10 litters for each of
ductivity was evaluated 30-days postbreeding, the nine mating types were retained for farrow-
at farrowing, at 21-days postfarrowing and hag with the remaining gilts slaughtered. This
when litters were weaned at 42-days of age. resulted in 74 gilts being slaughtered and 90
litter records for fall 1971.
Because of management difficulties in the
Materials and Methods fall 1971. farrowing season, excessive post-far-
rowing losses occurred and sows and gilts that
Data for this study came from the first phase farrowed in the season were remated in late
of the Oklahoma swine crossbreeding project winter to farrow in summer 1972. These sows
being conducted at the Ft. Reno Experiment were randomly mated.in the same manner as
Station. Purebred Durocs, Hampshires and described for the other seasons to a new group
Yorkshires were mated in all combinations to of boars of each breed. No sows were slaugh-
produce purebred and two-breed cross litters. tered and 71 litters from this season are
The formation and maintenance of the founda- included in the analyses.
tion herds from which the boars and gilts came All litter records for all sows in fall 1971 and
was previously described by Johnson, Omtvedt summer 1972 were adjusted to a gilt equivalent
and Waiters (1973). based on the observed differences between sows
The present study included 301 gilts and and gilts in fall 1971. Adjustments were made
139 sows. Fifty-nine of these females were from the average difference between observed
considered to have reproductive failures and the means for sows and gilts of each breed type.
data of 12 were not used because of injury, The average difference for each trait was
illness or disease to the dam. Of the remaining subtracted from the observed value for all sow
females, 119 were gilts slaughtered 30 days litters. The adjustments were 0.15, 0.49 and
postbreeding (39 with purebred and 80 with 0.46 for number of pigs per litter, 1.59, 7.32
crossbred embryos) and 250 farrowed litters and 14.85 kg for litter weight and 0.18, 0.98
(89 purebred and 161 crossbred). Gilts slaugh- and 1.94 kg for average pig weight per litter at
tered 30-days postbreeding were evaluated for birth, 21 and 42 days, respectively, and 4.17%
number of corpora lutea, number of live embry- for survival rate from birth to weaning. The
os, ratio of number of live embryos to the total same adjustment factor was used for sows of all
number of corpora lutea and embryo length in breed groups; however, it is possible the differ-
millimeters. Litter records were evaluated in ence between sows and gilts may depend on the
terms of litter size, total litter weight and breed involved. Numbers in this study were too
average pig weight per litter (unadjusted for small to detect this.
litter size) at 0, 21 and 42 days and the Estrus was detected with the assistance of a
percentage of number of pigs weaned of the teaser boar and hand mating was used in all
pigs farrowed per litter (survival rate.) seasons. The gilts and sows were maintained
The basic plan for this phase of the study throughout the gestation period in dry lots
was to mate each of six boars of each breed to equipped with individual feeding stalls in
REPRODUCTION OF PUREBREDS AND CROSSES 1281
groups of 16 head per lot. They were brought litter in the ijk~th subclass, p = fitted mean, R i
to the farrowing crates and then moved with = effect o f the itla season, ~ = effect of the j m
their litters to a nursery barn 3 to 7 days after sire breed, Sk(i) = effect o f the kth sire in the
farrowing. Sows and litters were maintained in jth sire breed, Ds = effect o f the ~th dam
the nursery, one litter per pen, until weaned at breed, (RB)ij, (RD)i s (BD)js and (RBD)ij~ =
42 days of age. The pigs were given access to interaction effects and eijks m = random ele-
creep feed after the 21-day weights were ment. All effects except Sk(i) and eiiks m are
obtained. considered fixed effects and Sl~.(j) and e~ik~mare
The gilts used to study ovulation rates and considered random effects witli ~ero m~ans and
early embryo development were slaughtered variances a3 and a ~, respectively. The mean
approximately 30-days postbreeding on a week- squares and degrees of freedom for sire effects
ly basis. The entire reproductive tract was and residual only from these analyses are
recovered, the ovaries removed and the number presented in table 2. Sire mean squares were
of corpora lutea counted. The embryos were not significant for any trait suggesting that the
removed, counted and crown-rump measure- sire component of variance is zero or quite
ments made while embryos were still enclosed small for these traits. Reddy, Lasley and Mayer
in the amnion. Gilts returning to estrus after (1958) also demonstrated that sires were not an
being mated during each estrus throughout the important source of variation for litter size. Sire
8-week breeding period were also slaughtered effects, were then deleted from the model and
and their reproductive tracts observed for gross all 30-day postbreeding traits, except number
abnormalities. of corpora lutea, and litter traits from birth to
Records on all gilts and sows that farrowed weaning were analyzed by least squares accord-
at least one live pig are included except records ing to the reduced model with the effects as
of nine sows and gilts that had serious diffi- described above. For the trait average embryo
culties at parturition or that had been injured length per litter 30-days postbreeding the par-
or ill prior to parturition or shortly after tial regression of embryo length on days preg-
parturition such that the entire litter was lost. nant was added to the model. The model for
The records of three gilts slaughtered 30-days number o f corpora lutea per gilt included only
post-breeding were deleted because o f serious the effects of season, breed of dam and their
injury prior to slaughter. interaction.
All litter traits from birth to weaning were The primary interest in this phase of the
subjected to a preliminary analysis to determine study was the performance o f a purebred dam
the importance o f sire effects. The data were of each breed when mated pure as compared to
analyzed by least squares according to the when mated to a boar o f another breed. F o r
following model: Yijklm = P + Ri + Bi + each trait least squares means and specific
( R B ) i j + Sk(j)+ Ds + (RD)i~ +(BD)j~ + comparisons among means were made from
(RBD~ijs + eiiks where Yiiks = observed linear functions o f the least squares estimates of
value of the ~dependent variable for the mth the effects in the model.
1282 JOHNSON AND OMTVEDT
TABLE 2. DEGREES OF FREEDOM AND MEAN SQUARES FOR SIRES AND ERROR F O R LITTER
TRAITS FROM BIRTH TO WEANING
Breed of dam
Item Duroc Hampshire Yorkshire
No. of females selected to be mated 149 146 145
No. of gilts slaughtered pregnant 43 42 38
No. of gilts that farrowed 50 52 39
N o . o f open giltsa 7 6 24
No. of sows that farrowed 41 42 34
No. of open sowsa 8 4 10
Total no. of reproductive failures 15 10 34
Percent of females selected to be mated that failed 10.1 6.8 23.4
a I n c l u d e s aH that were never observed in estrus plus t h o s e bred but not pregnant.
REPRODUCTION OF PUREBREDS AND CROSSES 1283
TABLE 4. ANALYSES OF VARIANCE FOR NUMBER OF CORPORA LUTEA, NUMBER OF LIVE
EMBRYOS, PERCENT LIVE EMBRYOS OF CORPORA LUTEA AND AVERAGE EMBRYO
LENGTH FOR GILTS SLAUGHTERED 30-DAYS POSTBREEDING
sire b y breed o f dam interaction for all traits regressions provided no evidence for a quadratic
were generally small in comparison to the response within the range o f days o f pregnancy
respective error mean square. This suggests the at the time o f slaughter in this study ( ~ =
sire breed is relatively unimportant for the dam 29.15, SD = 2.68 days).
productivity traits measured 30-days postbreed- The least squares mating-type means, stan-
ing. The mean squares for interaction o f season dard errors and specific comparisons among
with other effects in the model were generally means for the embryo data are presented in
smaller than the error mean squares providing table 5. Differences in ovulation rates for the
no evidence for interactions o f any effect with three breeds were observed. Duroc and York-
season in these data. The :partial regression shire gilts each averaged 13.8 corpora lutea,
coefficient o f average embryo length on the which was 1.7 corpora lutea per gilt more (P <
number o f days pregnant was 1.55 -+ .116 mm. .01) than that observed for Hampshire gilts.
Simultaneous fitting o f the linear and quadratic Since gilts of each breed were approximately
TABLE 5. LEAST SQUARES BREEDING GROUP MEANS AND STANDARD ERRORS AND
SPECIFIC COMPARISONS AMONG MEANS FOR LITTER TRAITS OF GILTS
SLAUGHTERED 30-DAYS POSTBREEDING
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REPRODUCTION OF PUREBREDS AND CROSSES 1287
21-day pig weight for Hampshires were about Cunningham, 1967). None of the differences
the same as for Yorkshires, and 0.25 kg heavier between average pig weight per litter for pure-
than those for Durocs, but the pigs raised by breds and crossbreds in the present study were
Hampshires had the lightest 42-day weights. significant and all did not favor crossbreds. On
the average crossbred pigs weighed 0.01 + .04
kg more than purebreds at birth and 0.12 +
.25 kg more at weaning. This represents a
Discussion relatively small increase o f 0.9% at farrowing
and 1.23% at 42-days in average pig weight per
Squires, Dickerson and Mayer (1952) re- litter for crossbred litters over purebred litters.
ported outbred Durocs to have 11.85 corpora However, due to the increased litter size,
lutea and 8.03 normal embryos and inbred crossbred litters were 17.9 and 20.8% heavier at
Hampshires to have 11.43 corpora lutea and birth and weaning, respectively, than purebred
6.73 normal embryos when gilts were slaugh- litters.
tered 25-days postbreeding. These breed dif- These data suggest some response to cross-
ferences were not statistically significant and breeding in early embryo development; how-
not as large as reported in the present study. ever, the primary response to crossbreeding
Reddy et al. (1958) slaughtered purebred appears to be in litter size at birth and weaning
Duroc gilts 55-days postbreeding and reported and a greater survival rate for crossbred pigs
ovulation rate and number o f live embryos to than for purebred pigs. This response in the
be 8.7 -+ .75 and 6 . 6 - + 1.51, respectively. present study was due primarily to an in-
These values are considerably lower than those creassed livability throughout gestation and
obtained in the present study. from birth to weaning in crossbred litters
The average advantage of crossbred litters produced by Duroc and Hampshire dams. Pigs
over purebred litters in number o f pigs per litter raised by Yorkshire dams had the highest
at 0, 21 and 42 days was 0.81 + .36, 1.00 + .30 survival rates and there was no difference in
and 1.06 + .30 pigs per litter, respec- livability between purebred and crossbred lit-
tively. This represents an 8.68% advantage in ters from Yorkshire dams.
litter size at birth and a 17.86% advantage in
number weaned for 2-breed cross litters over
purebred litters. Survival rate was also 8 . 0 3 -
3.22% higher for pigs in crossbred litters than
for pigs in purebred litters. These crossbred Literature Cited
advantages for number o f pigs per litter and the Alschwede, W. T. and O. W. Rob~son. 1971. Prenatal
increased survival rate of crossbred pigs are in and postnatal influences on growth and backfat in
general agreement with several reports in the swine. J. Anim. Sci. 32:10.
literature (Winters et al., 1935; Craft, 1953; Bradford, G. E., A. B. Chapman and R. H. Grummer.
1958. Effects of inbreeding, selection, linecrossing
England and Winters, 1953; Whatley, Chambers and topcrossing in swine. III. Predicting combining
and Stephens, 1954; Smith and McLaren, ability and general conclusions. J. Anita. Sci.
1967). However in the present study, most of 17:456.
the crossbred superiority was due to mating Conover, W. J. 1971. Practical nonparametric statis-
tics. John Wiley and Sons Inc., New York.
Duroc and Hampshire dams to a boar of Craft, W. A. 1953. Results of swine breeding research.
another breed, while Yorkshire dams performed U.S.D.A. Cir. No. 916.
nearly the same whether producing purebred or Cunningham, P. J. 1967. Crossbreeding effects on
crossbred litters. Although mating-type com- preweaning and postweaning performance in swine.
M.S. Thesis. Oklahoma State University, Stillwater.
parisons within each breed of dam for number Dickerson, G. E., C. T. Blunn, A. B. Chapman, R. M.
o f embryos 30-days postbreeding were not Kottman, J. L. Krider, E. J. Warwick and J. A.
significant, they were in the same direction and Whatley, Jr. 1954. Evaluation of selection in
of approximately the same magnitude for each developing inbred lines of swine. Mo. Agr. Exp.
Sta. Res. Bull. 551.
breed of dam as were the traits from birth to England, D. C. and L. M. Winters. 1953. The effects of
weaning. This lends further support to the genetic diversity and performance of inbred lines
hypothesis that dams of these three breeds per se on hybrid vigor in swine. J. Anita. Sci.
exhibit a different response to crossbreeding in 12:836.
litter size. Johnson, R. K., I. T. Omtvedt and L. E. Waiters. 1973.
Evaluation of purebreds and two-breed crosses in
Previous workers have reported crossbred swine: Feedlot performance and carcass merit. J.
pigs to be heavier than purebred pigs at birth Anim. Sci. 37:18.
and at weaning (Winters et al., 1935; Lush et Lush, J. L., P. S. Shearer and C. C. Culbertson. 1939.
al., 1939; England and Winters, 1953; Crossbreeding hogs for pork production. Iowa Agr.
1288 JOHNSON AND OMTVEDT
Exp. Sta. Bull. 380. sows on sexual maturity, rate of ovulation, fertil-
O'Feirall, G. J. More, H. O. Hetzer and J. A. Gaines. ization and embryonic survival. Mo. Agr. Exp. Sta.
1968. Heterosis in preweaning traits of swine. J. Res. Bull. 494.
Anim. Sci. 27:17. Smith, H. G. and J. B. McLaren. 1967. Performance of
Reddy, V. B., J. F. Lasley and D. T. Mayer. 1958. breeds and breed crosses of swine. Tenn. Agr. Exp.
Genetic aspects of reproduction in swine. Mo. Agr. Sta. Bull. 434.
Exp. Sta. Res. Bull. 666. Whatley, J. A., Jr., D. Chambers and D. F. Stephens.
Robison, W. L. 1948. Crossbreeding for the produc- 1954. Using hybrid vigor in producing market pigs.
tion of market hogs. Ohio Agr. Exp. Sta. Res. Bull. Okla. Agr. Exp. Sta. Bull. 415.
675. Winters, L. M., O. M. Kiser, P. S. Jordan and H. W.
Squires, C. P., G. E. Dickerson and D. T. Mayer. 1952. Peters. 1935. A six years study of crossbreeding
Influence of inbreeding, age and growth rate of swine. Minn. Agr. Exp. Sta. Bull. 320.