To determine what, if any, effects exposure to ultrasonic beams has on preimplantation embryos we iso· lated mouse blastocysts and assessed resorption rate, pregnancy rate, decidual swelling volume, and live birth rate after in vitro exposure with subsequent transfer to surrogate mothers. The blastocyst stage embryos were isolated by flushing the uteri of pregnant animals with a phosphate buffered medium. Blastocysts at a discrete stage of development were pooled and transferred to a PBl ·methykellulose medium. This medium is specifically designed to maintain the embryos in a high viscosity solution during the sonographic expo· sure to prevent microcavitation. After the exposure, the embryos were washed free of methylcellulose and T he commonly held notion that the preimplantation embryo is safe from the noxious effects of chemical disruption has been shown to be an oversimplification. u The blastocyst stage of the preimplantation embryogenesis is a period of critical genetic determination and differentiation? It is incorrect to assume that this period is not susceptible to subtle nonlethal mutations that may result in poor pregnancy outcome, including dysmorphogenesis.4-B Recently our group and others have confirmed that transferred to the uteri of pseudopregnant surrogate mothers. A total of 660 blastocyst stage embryos were distributed among seven treatment groups. After exposure, the embryos were transferred to 54 surrogate mothers. A total of 199 embryos were implanted successfully for postimplantation evaluation. An additional 427 blastocysts were distributed among four treatment groups and transferred to 46 surrogate moth· ers to assess the effect of sonographic exposure on birth rate. The results indicate possible deleterious effects (decreased implantation rate, increased resorption rate, decreased decidual swelling volume, and increased stillbirth rate) of short ultrasonic exposures (1 min and 5 min) on mouse blastocyst function.exposure to methylnitrosourea (MNU), a direct-acting mutagen, can result in significant postimplantation dysmorphogenesis after exposure in the preimplantation stage-that is, during middle to late gestation but Jong after the exposure.