Ever since Bard (1928) demonstrated on cats that rage reactions readily develop after decortication and transection of the brain stem at the level of the diencephalon, the attention of workers has been directed toward the role played by the diencephalon and mesencephalon in the government of these reactions. Ranson & Magoun (1933) by electrical stimulation of the hypothalamus in cats with the head fixed in a stereotaxic apparatus obtained spitting; Magoun, Atlas, Ingersoll & Ranson (1937) from the central gray matter of the mid-brain and the adjacent tegmentum produced hissing and crying. On the waking, freely moving cat, Hess & Briigger (1943) elicited an affective defence reaction, i.e. hissing, lowering of the head, flattening of the ears, marked dilatation of the pupils, and pilo-erection on back and tail, by stimulation of the 'perifornical' region of the hypothalamus. Flight responses have also been produced by stimulation of the posterior hypothalamus and the adjacent subthalamic region (Hess, 1949(Hess, , 1957. Hunsperger (1956) obtained the affective defence reaction, not only from the 'perifornical' region of the hypothalamus, but also from the central gray matter of the mid-brain, these two areas being surrounded by a larger common field from which flight responses were obtained. It was therefore concluded that the substratum concerned with these various patterns of emotional behaviour constitutes an unbroken field, comprising portions of the central gray matter of the preoptic area, the hypothalamus and the mid-brain. The reactions were strikingly similar to those seen when a cat is confronted by a dog, but did not appear to be the pain-suggestive reactions reported by Spiegel, Kletzkin & Szekely (1954) in the unrestrained cat, and by Delgado (1955)