No abstract

1. The dynamic analysis of the control exerted by neck and macular vestibular receptors on the cerebellar cortex has been investigated in precollicular decerebrate cats submitted to sinusoidal rotation along the longitudinal axis of the animal at the frequency of 0.026 Hz and at peak amplitudes up to 10 degrees for the neck input and 15 degrees for the macular input. 2. Purkinje (P) cells located in the vermal cortex of the cerebellar anterior lobe, particularly in the longitudinal parasagittal zone which projects to the ipsilateral lateral vestibular nucleus (LVN), showed a sinusoidal modulation of the firing rate in response to sinusoidal stimulation of the neck receptors or the vestibular receptors, the phase of the responses being in most units related to the extreme neck or head position. Mossy fiber (MF) and/or climbing fiber (CF) responses of the same or different P-cells to the two inputs were observed. 3. The sensitivity of the MF-response of the P-cells to the neck input, elicited by sinusoidal rotation of the neck and expressed in per cent of the average firing rate per degree of neck rotation, corresponded on the average to 2.71 +/- 1.67, S.D. This value was significantly higher than that of the MF-response of the P-cells to the macular input elicited by sinusoidal tilt along the longitudinal axis of the whole animal, which correspond to 1.71 +/- 1.01, S.D. 4. Most of the MF-responses of the P-cells to the neck input were characterized by an excitation during side-down rotation of the neck and by an inhibition during side-up rotation, whereas most of the MF-responses of the P-cells to the macular input showed just the opposite behavior, being inhibited by side-down tilt of the animal and excited by side-up tilt. 5. Units which received a convergent input from both neck and macular receptors and showed an antagonistic pattern of response to the two inputs were tested during rotation of the head alone, in order to excite simultaneously the two kinds of receptors. Due to the higher sensitivity of the neck over the macular response, the magnitude of the combined response tended to be similar to the difference between the individual ones. Moreover, the phase of the resulting response was always modified with respect to that of the response to the neck input alone, and became in some instances related to velocity of neck rotation rather than to neck position. 6. These findings indicate that opposite responses to neck and macular inputs occur at corticocerebellar level. However, a final integration of the two inputs, leading to suppression of the conflicting responses, may occur either at medullary (LVN) or at spinal cord level.

The dependence of solar rotation on the size of the chromospheric tracers is considered. On the basis of an analysis of Ca n K3 daily filtergrams taken in the period 8 May-14 August, 1972, chromospheric features can be divided into two classes according to their size. Features with size falling into the range 24 000-110 000 km can be identified with network elements, while those falling into~the range 120 000-300 000 km with active regions, or brightness features of comparable size present at high latitudes. The rotation rate is determined separately for the two families of chromospheric features by means of a cross-correlation technique which directly yields the average daily displacement of tracers due to rotation. Before computing the cross-correlation functions, chromospheric brightness data have been filtered with appropriate bandpass and highpass filters for separating spatial periodicities whose wavelengths fall into the two ranges of size, characteristic of the network pattern and of the activity centers. A difference less than 1% of the rotation rate of the two families of chromospheric features has been found. This is an indication for a substantial corotation at chromospheric levels of different short-lived features, both related to solar activity and controlled by the convective supergranular motions. 18 E. ANTONUCCI ET AL.