_The acts of all the centres involve the use of the same muscles._ When a headless frog's hind leg wipes the acid, he calls into play all the leg-muscles which a frog with his full medulla oblongata and cerebellum uses when he turns from his back to his belly. Their contractions are, however, _combined_ differently in the two cases, so that the results vary widely. We must consequently conclude that specific arrangements of cells and fibres exist in the cord for wiping, in the medulla for turning over, etc. Similarly they exist in the thalami for jumping over seen obstacles and for balancing the moved body; in the optic lobes for creeping backwards, or what not. But in the hemispheres, since the presence of these organs _brings no new elementary form of movement_ with it, but only _determines differently the occasions_ on which the movements shall occur, making the usual stimuli less fatal and machine-like; we need suppose no such machinery _directly_ co-ordinative of muscular contractions to exist. We may rather assume, when the mandate for a wiping-movement is sent forth by the hemispheres, that a current goes straight to the wiping-arrangement in the spinal cord, exciting this arrangement as a whole. Similarly, if an intact frog wishes to jump over a stone which he sees, all he need do is to excite from the hemispheres the jumping-centre in the thalami or wherever it may be, and the latter will provide for the details of the execution. It is like a general ordering a colonel to make a certain movement, but not telling him how it shall be done.[5] _The same muscle, then, is repeatedly represented at different heights;_ and at each it enters into a different combination with other muscles to co-operate in some special form of concerted movement. _At each height the movement is discharged by some particular form of sensorial stimulus._ Thus in the cord, the skin alone occasions movements; in the upper part of the optic lobes, the eyes are added; in the thalami, the semi-circular canals would seem to play a part; whilst the stimuli which discharge the hemispheres would seem not so much to be elementary sorts of sensation, as groups of sensations forming determinate _objects_ or _things. Prey_ is not pursued nor are _enemies_ shunned by ordinary hemisphereless frogs. Those reactions upon complex circumstances which we call instinctive rather than reflex, are already in this animal dependent on the brain's highest lobes, and still more is this the case with animals higher in the zoological scale. The results are just the same if, instead of a frog, we take a pigeon, and cut out his hemispheres as they are ordinarily cut out for a lecture-room demonstration. There is not a movement natural to him which this brainless bird cannot perform if expressly excited thereto; only the inner promptings seem deficient, and when left to himself he spends most of his time crouched on the ground with his head sunk between his shoulders as if asleep.