SUMMARY1. Compound action potentials were recorded from certain muscle and cutaneous nerves in normal and chronically de-efferentated hind limbs of cats during stimulation of the appropriate dorsal spinal roots.2. The peaks for groups I, II and III in the compound action potential were correlated with the corresponding peaks in the fibre-diameter histograms of the same de-efferentated nerve after processing it for light microscopy.3. The scaling factor (ratio of conduction velocity in m/sec to total diameter in gm) was not constant for all sizes of fibre nor did it increase progressively with fibre size. Evidence is presented that a logarithmic relation between conduction velocity and fibre diameter is not appropriate. 4. In muscle nerves the scaling factor for fibres fixed by glutaraldehyde perfusion and embedded in Epon was 5-7 for group I afferent fibres and 4-6 for myelinated fibres in both group II and group III.

SUMMARY1. The ultrastructure of all the afferent fibres, or all the efferent fibres, was studied in selected nerves from chronically de-afferentated or de-efferentated cat hind limbs perfusion-fixed with glutaraldehyde.2. The following parameters were measured: number of lamellae in the myelin sheath (n), axon perimeter (s), external fibre perimeter (S), axon cross-sectional area (A). Fibres were allocated to afferent groups I, II, III or efferent groups a and y according to the number of lamellae in the myelin sheath.3. of axon so that m = 2-58 log10 s -1t73. The interpretation that there are two separate linear relations for large and small fibres is favoured. 6. The ratio of axon to external fibre perimeter (g) falls from about 0 70 for group III and small y fibres in the cat to about 0-62 for group II and large y fibres and then rises again to 0'70, or even 0-75 for group I and a axons. (Hursh, 1939;Lubinska, 1960; Coppin, 1973) and between I and 0 (Coppin & Jack, 1972).8. From the theoretical analyses of Rushton (1951) and others 0 should be proportional to the external dimensions of the fibre rather than to axon size. It is shown

SUMMARY1. One hind limb of each of four cats was either chronically de-efferentated, or chronically de-afferentated, and perfused with buffered glutaraldehyde fixative. Up to three different muscle nerves were dissected from each limb, post-fixed in osmium tetroxide and embedded in Epon. Ultrathin transverse sections were mounted on Formvar-coated single-hole specimen grids so that all the fibres in each nerve could be examined individually by electron microscopy.2. Non-circularity was expressed as the ratio (0): axon cross-sectional area area of a circle with same perimeter'The degree of non-circularity of all the afferent axons, or all the efferent axons, in each muscle nerve was determined. The proportion of fibres cut through the paranodal region, or through the Schwann cell nucleus, was as expected for group I afferent and for a and y efferent fibres, but hardly any typical paranodal sections of group II or III afferent fibres were encountered which suggests that their paranodal arrangement differs from that of other groups. In a quantitative comparison of noncircularity in different functional groups, fibres cut through paranodes, Schwann cell nuclei or Schmidt-Lanterman clefts were rejected.3. All the y efferent fibres in one nerve were studied in a series of sections cut at 25 ,tm intervals. The degree of non-circularity was found to be relatively constant along the internode of most fibres when the values at paranodes, Schwann cell nuclei or Schmidt-Lanterman clefts were ignored.4. The value of 0 varied widely from 1-0 (circular) to 0-5 or less from fibre to fibre within every functional group. However, the mean value of qS was less for y axons (0.68) than for a axons (0.78), and less for group III axons (0.79) than for axons in groups I and II (both 0.84). When the results for all the nerves were aggregated, these differences were statistically very highly significant, as was the difference in qS between group I and a fibres. If values of qS < 0 5 were rejected, the difference between the between a and y fibres was still very highly significant. 5. The external perimeter (S) of a non-circular fibre differs from 2i times the diameter of a circle just enclosing the fibre (D). It is shown that S = 0 95 7TD for group I and II fibres, S = 0 90 nrD for a and group III fibres, and S = 0-85 iD for y fibres.6. The myelin period, or interperiod repeat distance, varied from 14 1 to 15-6 nm in different cats, implying radial shrinkage of the myelin sheath from 15 to 23% The myelin period in a particular cat was the same for several nerves, and the same for fibres in different functional groups.7. The possibility that repetitive firing of axons during fixation contributed to the varying degree of non-circularity is considered but rejected as unlikely.8. It is deduced that about 10 % radial shrinkage of the myelin sheath, but little or no osmotic shrinkage of the axon, occurred during fixation and rinsing. Further radial shrinkage of about 8 % in all components of the fibre probably occurred as a result of subsequen...