The perception of shape is independent of the size and position of the shape and also of the visual cue that defines it. The same shape can be recognized whether defined by a difference in luminance, by motion, or by texture. Experiments showed that the shape selectivity of individual cells in the macaque inferior temporal cortex did not vary with the size and position of a shape and also did not vary with the visual cue used to define the shape. This cue invariance was true for static luminance and texture cues as well as for relative motion cues--that is, for cues that are processed in ventral and dorsal visual pathways. The properties of these inferior temporal cells meet the demands of cue-invariant shape coding.

In this study, we compared the organization of orientation preference in visual areas V1, V2, and V3. Within these visual areas, we also quantified the relationship between orientation preference and cytochrome oxidase (CO) staining patterns. V1 maps of orientation preference contained both pinwheels and linear zones. The location of CO blobs did not relate in a systematic way to maps of orientation; although, as in other primates, there were approximately twice as many pinwheels as CO blobs. V2 contained bands of high and low orientation selectivity. The bands of high orientation selectivity were organized into pinwheels and linear zones, but iso-orientation domains were twice as large as those in V1. Quantitative comparisons between bands containing high or low orientation selectivity and CO dark and light bands suggested that at least four functional compartments exist in V2, CO dense bands with either high or low orientation selectivity, and CO light bands with either high or low selectivity. We also demonstrated that two functional compartments exist in V3, with zones of high orientation selectivity corresponding to CO dense areas and zones of low orientation selectivity corresponding to CO pale areas. Together with previous findings, these results suggest that the modular organization of V1 is similar across primates and indeed across most mammals. V2 organization in owl monkeys also appears similar to that of other simians but different from that of prosimians and other mammals. Finally, V3 of owl monkeys shows a compartmental organization for orientation selectivity that remains to be demonstrated in other primates.

Previously, it was suggested that a hypothalamic mechanism links somatotropin [growth hormone (GH)] secretion to sleep regulation, and this may explain the temporal correlation between GH release and nonrapid eye movement sleep (NREMS) on sleep onset. The purpose of these experiments was to study whether growth hormone-releasing factor (GRF), a hypothalamic peptide responsible for stimulation of GH secretion, also has the capacity to promote sleep in rats and rabbits. Artificial cerebrospinal fluid or GRF (human GRF-[1-40], 0.01, 0.1, and 1 nmol/kg) was intracerebroventricularly injected to rats at dark onset, and the electroencephalogram (EEG), brain temperature (Tbr), and motor activity were recorded for 24 h. Rabbits received the same doses of GRF during the light period, and sleep-wake activity was monitored for 6 h. GRF promoted NREMS and rapid eye movement sleep (REMS) and increased EEG slow-wave activity in both rats and rabbits. NREMS increased in postinjection hour 1 after low doses of GRF, whereas the effect was more prolonged after higher doses. REMS increased in response to the low and middle doses of GRF in postinjection hour 1 in rats and in hour 2 after each dose in rabbits. The diurnal rhythms of sleep-wake activity, motor activity, and Tbr were not affected in rats. Because GRF promotes sleep and also stimulates GH secretion, it is a likely candidate for linking GH secretion and sleep regulation.

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1. We recorded from neurons responsive to gratings in the inferior temporal (IT) cortices of macaque monkeys. One of the monkeys performed an orientation discrimination task; the other maintained fixation during stimulus presentation. Stimuli consisted of gratings based on discontinuities in luminance, relative motion, and texture. 2. IT cells responded well to gratings defined solely by relative motion, implying either direct or indirect motion input into IT, an area that is part of the ventral visual cortical pathway. 3. Response strength in general did not depend on the cue used to define the gratings. Latency values observed for the two static grating types (luminance- and texture-defined gratings) were similar, but significantly shorter than those measured for the kinetic gratings. 4. Stimulus orientation had a significant effect in 27%, 27%, and 9% of the cells tested with luminance-, kinetic-, and texture-defined gratings, respectively. 5. Only a small proportion of cells were orientation sensitive for more than one defining cue. The average preferred orientation for luminance and kinetic gratings matched; the tuning width was similar for the two cues. 6. Our results indicate that IT cells may contribute to cue-invariant coding of boundaries and edges. We discuss the relevance of these results to visual perception.

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Humans are able to recognize objects when surface details, such as colour, texture and luminance gradients, are not available. By systematically eliminating colour, texture, shading, contrast and inner contours from given objects, we tested whether certain shape-selective inferior temporal cortex (IT) neurons of awake rhesus monkeys remain selective for these objects as the surface information is reduced. In psychophysical experiments, we established that the rhesus monkey can identify the shape of a coloured object largely independently of its surface characteristics and, to a lesser degree, of its inner contours. Shape selectivity of the neurons does not change when texture and shading are concealed. The responsiveness of the neurons is also affected by the removal of these surface attributes. The IT neurons were found to respond highly similarly to objects brighter or darker than their background. Selectivity for shape is preserved when the contrast is reversed. Deletion of the inner contours, outlining the main parts of the objects, did not affect the responses and selectivity of the IT neurons. These findings indicate that the IT can contribute to the invariant perception of objects having different surface details.

In rats, brain temperature (Tbr) and core temperature (Tc) were recorded in parallel with the sleep-wake activity throughout the 24-h diurnal cycle, consisting of a 12-h light (L) and a 12-h dark (D) period. In order to characterize the temperature changes associated with the arousal states in the L and the D separately, (i) the average temperatures in wakefulness (W), non-rapid eye movement sleep (NREMS) and REM sleep (REMS), and at the transitions between the arousal states were calculated; (ii) the courses of temperatures before and after the transitions (falling asleep, awakening from NREMS or REMS, transition from NREMS to REMS) were determined; (iii) the rates of changes in Tbr and Tc were calculated for each state; and (iv) the correlations between the temperatures and the overall length of each arousal state, and between Tbr and Tc were studied. In both the L and D periods, Tbr and Tc decreased at the beginning of NREMS, then levelled off, and increased slightly before awakening. Apart from short arousals which did not affect temperature, Tbr and Tc increased in W, peaked 15-20 min after awakening, and declined significantly before the falling asleep. In REMS, Tbr increased at a high rate, while a slight increase in Tc was evident in the L only. Correlations between the temperatures and the arousal states were found in both the L and the D. The courses of Tbr and Tc were also correlated. The results support the existence of characteristic changes in body temperature related to the arousal states in the rat.