In a Prolific Merino nucleus herd of 200 ewes the ovulation rate (OR) test
results obtained in 169 animals between 1988 and 1993 were compared with th
ose of 113 ewes from the same herd in 1996. Whereas earlier the ratio of in
dividuals showing an OR greater than or equal to 4 was only 32%, that of th
e group checked in 1996 was 59%. This increase could be attributed to 40 ew
es, both of whose parents had proven to be homozygous carriers of the proli
fic gene. To develop the Prolific Merino breed, 21 Booroola Merino rams wer
e imported from New Zealand, and mostly their frozen semen was used. Of the
se rams, one was not a prolific gene carrier, 8 were homozygous carriers, 1
0 were heterozygous carriers and two had not been identified yet. Of the 36
home-bred rams, 9 proved to be homozygous by parents, 11 heterozygous, 8 h
omozygous, one proved to be a non-carrier, and 7 rams and their frozen seme
n were to be progeny tested. Six thousand doses of frozen semen from a tota
l of 33 animals (16 imported rams and their 17 home-bred offspring) are sto
red in plastic straws. Sixty-three % of this is semen reserve from rams of
the Fec(B)Fec(B) genotype, belonging to 10 ram lines. The remaining 37% is
gene reserve intended for creating homozygous ram lines. Only one ram (no.
3244) was bought for the nucleus herd, the other ram lines were introduced
into the herd by assortative mating, using intrauterine insemination. The a
verage conception rate found after 472 intrauterine inseminations was 53% w
ith large (occasionally 10-100%) individual ram differences.