We have studied the pattern of electrical currents through amebas (mainly Chaos chaos) with an ultrasensitive extracellular vibrating probe. Amebas drive both steady currents and current pulses through themselves. Relatively steady current with an average surface density of 0.1-0.2 muA/cm2 enters the rear quarter of an ameba and leaves its pseudopods. Streaming reversals are preceded by changes in this current pattern and the region with the largest new inward current becomes the new tail. Ion substitution studies suggest that some of the steady inward current is carried by calcium ions. Characteristic stimulated pulses of current sometimes follow the close approach of the vibrating probe to the side of an advancing pseudopod. Such a pulse enters the cytoplasm through a small patch of membrane near the probe (and seems to leave through the adjacent membrane), is usually followed by hyaline cap and then by pseudopod initiation, is calcium dependent, lasts about 5-10 s, and has a peak density of about 0.4 muA/cm2. Spontaneous pulses of similar shape and duration may enter or leave any part of an animal. They are much less localized, tend to have higher peak densities, and occur in physiological salt solutions at about 0.2-4 times per minute. Retraction of a pseudopod is always accompanied or preceded by a spontaneous pulse which leaves its sides.

It is shown that light lost by reflection before entering a clear and homogeneous sphere or infinite cylinder is precisely compensated by light retained within these bodies by internal reflection; compensation means that the total rate of light absorption by infinitely dilute photoreceptors as integrated through the whole of these bodies or even through any concentric or coaxial shell making them up is independent of surface reflection. In the Phycomyces sporangiophore this theorem precludes a reflection explanation of R , the polarization dependence of the light growth response. An alternative explanation based upon anisotropic absorption by the receptors is explored and found tenable. Formulae are derived for R in any transparent cylindrical cell as a function of the constants of anisotropic absorption by the photoreceptors taken as a group ( C H ' and C L '), of the radial position of the receptors, and of the refractive indices of the cell ( n ) and of the medium ( N ). It is inferred that the photoreceptors in the Phycomyces sporangiophore are most absorbent for light vibrating in the direction of a hoop around a barrel. Orientation of the receptors by linkage to the cell wall is then shown to be a plausible explanation of the inferred anisotropy. On the basis of anisotropic reception, it is predicted that R should be constant for any N > n , and it is shown how C H ', C, L ' and the radial position of the receptors may all be obtained from a careful determination of R as a function of N .