Development of sensitivity to global form and motion in macaque monkeys (Macaca nemestrina).

To explore the relative development of the dorsal and ventral extrastriate processing streams, we studied the development of sensitivity to form and motion in macaque monkeys (Macaca nemestrina). We used Glass patterns and random dot kinematograms (RDK) to assay ventral and dorsal stream function, respectively. We tested 24 animals, longitudinally or cross-sectionally, between the ages of 5 weeks and 3 years. Each animal was tested with Glass patterns and RDK stimuli with each of two pattern types--circular and linear--at each age using a two alternative forced-choice task. We measured coherence threshold for discrimination of the global form or motion pattern from an incoherent control stimulus. Sensitivity to global motion appeared earlier than to global form and was higher at all ages, but performance approached adult levels at similar ages. Infants were most sensitive to large spatial scale (Δx) and fast speeds; sensitivity to fine scale and slow speeds developed more slowly independently of pattern type. Within the motion domain, pattern type had little effect on overall performance. However, within the form domain, sensitivity for linear Glass patterns was substantially poorer than that for concentric patterns. Our data show comparatively early onset for global motion integration ability, perhaps reflecting early development of the dorsal stream. However, both pathways mature over long time courses reaching adult levels between 2 and 3 years after birth.

Normal development of pattern motion sensitivity in macaque monkeys.

We studied the development of sensitivity to complex motion using plaid patterns. We hypothesized, based on neurophysiological data showing a dearth of pattern direction-selective (PDS) cells in area medial temporal (MT) of infant macaques, that sensitivity to pattern motion would develop later than other forms of global motion sensitivity. We tested 10 macaque monkeys (Macaca nemestrina) ranging in age from 7 weeks to 109-160 weeks (adult). The monkeys discriminated horizontal from vertical pattern motion; sensitivity for one-dimensional (1D) direction discrimination and detection were tested as control tasks. The results show that pattern motion discrimination ability develops relatively late, between 10 and 18 weeks, while performance on the 1D control tasks was excellent at the earliest test ages. Plaid discrimination performance depends on both the speed and spatial scale of the underlying patterns. However, development is not limited by contrast sensitivity. These results support the idea that pattern motion perception depends on a different mechanism than other forms of global motion perception and are consistent with the idea that the representation of PDS neurons in MT may limit the development of complex motion perception.

Development of perceptual completion originates in information acquisition.

Adults have little difficulty perceiving objects as complete despite occlusion, but newborn infants perceive moving partly occluded objects solely in terms of visible surfaces. The developmental mechanisms leading to perceptual completion have never been adequately explained. Here, the authors examine the potential contributions of oculomotor behavior and motion sensitivity to perceptual completion performance in individual infants. Young infants were presented with a center-occluded rod, moving back and forth against a textured background, to assess perceptual completion. Infants also participated in tasks to assess oculomotor scanning patterns and motion direction discrimination. Individual differences in perceptual completion performance were strongly correlated with scanning patterns but were unrelated to motion direction discrimination. The authors present a new model of development of perceptual completion that posits a critical role for targeted visual scanning, an early developing oculomotor action system.

Development of object concepts in macaque monkeys.

One of the most interesting questions in cognitive development is how we acquire and mentally represent knowledge about objects. We investigated the development of object concepts in macaque monkeys. Monkeys viewed trajectory occlusion movies in which a ball followed a linear path that was occluded for some portion of the display while their point of gaze was recorded with a corneal-reflection eye tracker. We analyzed the pattern of eye movements as an indicator of object representation. A majority of eye movements of adult monkeys were anticipatory, implying a functional internal object representation that guided oculomotor behavior. The youngest monkeys lacked this strong internal representation of objects. Longitudinal testing showed that this ability develops over time providing compelling evidence that object concepts develop similarly in monkeys and humans. Therefore, the macaque monkey provides an animal model with which to examine neural mechanisms underlying the development of object representations.

Decay of prism aftereffects under passive and active conditions.

In prism adaptation, subjects adapt to new visuospatial coordinates imposed by wedge prisms that laterally displace the visual field. During this process, subjects develop and store new visuomotor coordinates in order to compensate for the displacement of visual stimuli. After the prisms are removed, subjects show an aftereffect in the opposite direction of the original perturbation. The aftereffect is a manifestation of the recently stored information. In the present article, we were interested in studying the properties of the aftereffect. Specifically, we investigated the fate of the aftereffect under active conditions with motor reafferences but without visual input, and during passive conditions without visual or motor reafferences. The results in the motor active condition show that motor reafference (proprioceptive or corollary discharge information) led to a faster, but incomplete, aftereffect decay. The results in the passive condition show a bimodal aftereffect behavior, with a fast decay within the initial minutes, followed by a sustained aftereffect up to 20 min later. These data suggests that two different memory processes may contribute to the aftereffect, one showing a fast decay mainly within 1 min, and another that shows a stable endurance for more than 20 min.

Olfactory dysfunction in hereditary ataxia and basal ganglia disorders.

In the present study the olfactory system of hereditary ataxia patients was tested using the smell identification test. Two previous findings suggested a possible olfactory impairment in these patients. First, an olfactory dysfunction has been found in different neurodegenerative diseases, and second, human functional imaging has shown cerebellar activation during olfaction. As an initial approach to determine if cerebellar ataxia impairs the olfactory process, cerebellar ataxia patients, along with basal ganglia patients, were tested. The results show an olfactory deficit in both basal ganglia and hereditary ataxia patients. Further exploration of the olfactory capacities in hereditary ataxia is necessary to elucidate the specific nature of the deficits.