arise as the fetus is squeezed and pitched by the contracting uterus (Ronca et aI., 1993), and maternal vocalizations can provide an auditory accompaniment to labor contractions (Vince, Billing, Baldwin, Toner, & Weller, 1985). At birth, as the fetus is compressed through the relatively small space comprising the birth canal and delivered into a cold extrauterine environment, cutaneous, vestibular, and thermal stimuli become more intense (Ronca et aI., 1993).Remarkably little is known about the extent to which perinatal organisms are able to sense the stimuli present within their habitat. This is due, in part, to our limited understanding of sensory function in perinatal mammals. It is known, however, that auditory stimulation is detected by the fetus in utero (humans: Decasper & Fifer, 1980;Decasper & Spence, 1986; sheep: Vince, 1979; Vince, Armitage, Shill ito-Walser, & Reader, 1982) and that chemosensory cues within amniotic fluid are important for successful first nipple attachment (rat: Pederson & Blass, 1982). These and other studies provide clear evidence that certain stimuli present in utero are indeed within the range offetal detection thresholds. Nevertheless, most previous investigations have relied on temporally remote postnatal expressions of prenatal sensory experiences and, therefore, do not provide direct access to fetal sensory function or experiential events as they exist in utero.There is extensive evidence for fetal sensory function when strong nonbiological stimuli are applied (e.g.,