During the oscillographic study of the mode of function of the semicircular canals of the ray (Lowenstein & Sand, 1940a, b), it became clear that the accessibility of the elasmobranch labyrinth and the satisfactory survival of preparations of the labyrinth in the isolated otic capsule opened up the possibility of an extension of the work to the otolith organs in the utriculus, sacculus and lagena. This has now been carried out in experiments described in the present paper.
METHODSMale and female rays of a wing span of 15-24 in. were killed by decapitation, pithing, and removal of the brain. The cranium was then isolated and the labyrinth approached through the cartilage at the back of the orbit or from the ventral side. Text- fig. 1 shows a ventro-lateral view of the membranous labyrinth after a maximum exposure of the otolith organs. Openings into the perilymphatic space of a much smaller extent were made for the exposure of individual receptors. In the case of the utriculus the approach was made from the orbit, and nerve twigs from the utricular nerve fan were cut at its proximal end and peeled up towards the lateral margin of the macula. The ampullary nerve branches supplying the anterior vertical and horizontal canals were divided in order to avoid the intrusion of spurious ampullary discharges.In the case of the ramus inferior the posterior ampullary nerve is well out of the way, and the sacculus can thus be isolated by transection of the free-running branch supplying the lagena. The latter is fortunately long enough to allow isolated pure lagena twigs to be peeled off for electrical pick-up. A choice of the region of the sacculus macula to be recorded from was possible owing to the convenient fanning out of the saccular branches of the ramus inferior. Very small twigs could be isolated which, as a rule, contained only a few functional units, the number of which could be further reduced, often to a single functional fibre, by careful crushing of the twig or by its further subdivision by splitting.When the desired twig had been prepared it was picked up in a silver-plated forceps electrode, held in position by a number of rods connected to the preparation holder by rotary clamps. The second electrode was applied to some inner part of the cranium. The holder was then clamped to a tilting device (Text- fig. 2) with the 'nose' pointing in any desired direction. The apparatus was designed for tilting movements about any horizontal axis desired, smoothness of movement and constancy of speed being assured by the use of a 50: 1 reduction gear operated by hand. The wheel at the left was graduated into 360 degrees for the accurate reading of the tilting angle. The slotted