Abstract. The objective was to determine whether aging of sperm caused by incubation at normothermic (38.5 C) or heat shock (40 C) temperatures for 4 h prior to oocyte insemination affects sperm motility, fertilizing ability, competence of the resultant embryo to develop to the blastocyst stage and blastocyst sex ratio. In the first experiment, the percent of sperm that were motile was reduced by aging (P<0.001) and the reduction in motility was greater for sperm at 40 C compared to sperm at 38.5 C (P<0.01). In the second experiment, oocytes were inseminated with aged sperm. A smaller percent of oocytes fertilized with sperm aged at either temperature cleaved by Day 3 after insemination than oocytes fertilized with fresh sperm (P<0.05). There was no effect of sperm aging on the percent of oocytes or cleaved embryos that developed to the blastocyst stage. Aging of sperm before fertilization at 38.5 C reduced the percent of blastocysts that were male (P=0.08). In the third experiment, incubation of sperm at 38.5 C or 40 C for 4 h did not reduce fertilizing ability of sperm as determined by pronuclear formation at 18 h post insemination. In conclusion, aging of sperm reduced cleavage rate and the percent of blastocysts that were males but had no effect on the developmental capacity of the embryo. The effect of aging on cleavage rate may represent reduced motility and errors occurring after fertilization and pronuclear formation. Aging at a temperature characteristic of maternal hyperthermia had little additional effect except that polyspermy was reduced. Results indicate that embryo competence for development to the blastocyst stage is independent of sperm damage as a result of aging for 4 h at normothermic or hyperthermic temperatures. Key words: Aging, Bovine, Fertilization, Heat shock, Spermatozoa (J. Reprod. Dev. 55: [69][70][71][72][73][74] 2009) evelopmental competence of the mammalian embryo is dependent on genetic and non-genetic contributions from its parents [1][2][3][4][5][6]. Sperm could affect an embryo's competence for development if the timing of fertilization or early cleavage is delayed. For example, embryos produced by high-fertility bulls entered S-phase of the first cell cycle earlier and had a longer S-phase than those produced by low-fertility bulls [7]. In another study, spermatozoa from 50% of bulls identified as being of low fertility in artificial insemination studs experienced premature capacitation [8]. Damage to the macromolecular portions of the sperm that are incorporated by the embryo could also result in formation of embryos with reduced developmental competence. Among these sperm contributions are DNA, the centriole [9], and RNA [10]. Embryos fertilized with semen containing a high proportion of sperm with extensive DNA damage have reduced competence for development [11][12][13] but the importance of damage to the centriole or sperm RNA is not known.Damage to sperm can occur in the male reproductive tract or after deposition of sperm in the female. In bulls, for example, thermal...