Summary: We examined the relationship between eye movement direction in REM sleep recorded by electrooculograph (EOG) and gaze direction in dream imagery. In a double-blind protocol, carefully screened and trained subjects were awakened subsequent to direct coupled EOG activity that was either predominantly horizontal or vertical. Following a target eye movement that fulfilled predetermined amplitude and directional criteria, a brief period of ocular quiescence was allowed to transpire before the subject was awakened. The dream narratives and EOG activity occurring prior to the REM awakenings were each reduced to a series of quantitatively scaled ratings. Analyses of variance demonstrated that when the confidence level of the experimenters' prediction is taken into account, statistically significant relationships exist between the number and direction of shifts of gaze in the dream report and scaled measurements of the corresponding EOG. When given dream narratives and the corresponding EOG recordings in sets of four, judges were unable to match them correctly better than by chance. However, in the above matching, judges significantly paired the dream narratives with EOG recordings that were in the same axis of gaze. Key Words: Eye movements-Dream imagery-REM sleep-Saccades-Oculomotor system.The relationship between dreaming and concurrent oculomotor activity during sleep constitutes a model problem for mentation and physiology. The enigmatic appearance of saccadic eye movements at regular intervals in the sleep cycle raises conjectures about their relationship to dreaming. Aserinsky and Kleitman (1) reported a temporal contiguity between eye movements and dreaming in 20 normal subjects. They concluded that both the ocular activity and the dreaming were temporally related to periods

Arginase from the liver of Xenopus laevis has been purified to homogeneity by heat treatment, acetone fractionation, and isoelectric focussing. The main component had an isoelectric point (I.E.P.) of 7.3; there is a minor component of I.E.P. 7.8. The molecular weight of the enzyme, as determined by gel filtration on Sephadex G200, is 76,000 daltons, substantially less than that of rat liver arginase studied concurrently. The molecular weight of the subunits, as determined by electrophoresis in sodium dodecyl sulfate, is 18,000 daltons, again less than that of rat liver arginase. The data indicate that Xenopus liver arginase, like rat liver arginase, is a tetramer. The molecular weight of arginase from adult Xenopus laevis corresponds to that from larval Rana esculenta.

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