The nature of subfertility due to the male or inseminate is as complex as t
hat of the female. Fertilization failure or failure in embryogenesis are bo
th documented to be of seminal origin. Males also differ in the numbers of
sperm required to reach their maximum fertilization rate. Males requiring m
ore sperm would be considered to have compensable seminal deficiencies. The
se include a number of known (viability and morphology) and unknown factors
(functional or molecular traits) precluding sperm access to the ovum or ab
ility to engage the ovum sufficiently to initiate fertilization and the blo
ck to polyspermy. Differences in fertility among males or inseminates indep
endent of sperm dosage are considered uncompensable. These deficiencies wou
ld be associated with fertilizing sperm that are incompetent to maintain th
e fertilization process or subsequent embryogenesis once initiated, with mo
st failures occurring prior to maternal recognition of pregnancy. Such sper
m would preempt fertilization by competent sperm. Chromatin aberrations in
morphologically normal or near normal spermatozoa from abnormal semen sampl
es appear to be the best candidates for the uncompensable deficiency. Howev
er, recognition of uncompensable or incompetent fertilizing sperm has not b
een achieved. Six-day-old non-surgically recovered bovine ova/embryos have
been used to evaluate compensable and uncompensable seminal deficiencies as
well as to test reproductive strategies. These ova/embryos provide informa
tion on fertilization status and embryo quality as well as quantitative and
qualitative data regarding associated accessory sperm. Thus, they permit t
he separation of reproductive failure by fertilization from that by embryon
ic development. Accessory sperm number is positively associated with both f
ertilization rate and embryonic quality. Early insemination results in low
fertilization rates (low accessory sperm number), but good embryo quality,
whereas, late insemination results in high fertilization rates (high access
ory sperm number), but poor embryo quality. Additional studies will be nece
ssary to substantiate this model; however, if true, future research designe
d to improve results to artificial insemination should be tested by breedin
g early in estrus where sperm viability is most limiting and embryo quality
is best. (C) 2000 Elsevier Science B.V. All rights reserved.