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C R Olson

Publications and source records attributed to C R Olson.

At least 37 records · Page 2Linked to original sources

Topographical organization of cortical afferents to extrastriate visual area PO in the macaque: a dual tracer study.

We have examined the origin and topography of cortical projections to area PO, an extrastriate visual area located in the parieto-occipital sulcus of the macaque. Distinguishable retrograde fluorescent tracers were injected into area PO at separate retinotopic loci identified by single-neuron recording. The results indicate that area PO receives retinotopically organized inputs from visual areas V1, V2, V3, V4, and MT. In each of these areas the projection to PO arises from the representation of the periphery of the visual field. This finding is consistent with neurophysiological data indicating that the representation of the periphery is emphasized in PO. Additional projections arise from area MST, the frontal eye fields, and several divisions of parietal cortex, including four zones within the intraparietal sulcus and a region on the medial dorsal surface of the hemisphere (MDP). On the basis of the laminar distribution of labeled cells we conclude that area PO receives an ascending input from V1, V2, and V3 and receives descending or lateral inputs from all other areas. Thus, area PO is at approximately the same level in the hierarchy of visual areas as areas V4 and MT. Area PO is connected both directly and indirectly, via MT and MST, to parietal cortex. Within parietal cortex, area PO is linked to particular regions of the intraparietal sulcus including VIP and LIP and two newly recognized zones termed here MIP and PIP. The wealth of connections with parietal cortex suggests that area PO provides a relatively direct route over which information concerning the visual field periphery can be transmitted from striate and prestriate cortex to parietal cortex. In contrast, area PO has few links with areas projecting to inferior temporal cortex. The pattern of connections revealed in this study is consistent with the view that area PO is primarily involved in visuospatial functioning.

Animals↗

Organization of cortical and subcortical projections to area 6m of the cat.

By analyzing regional variations of afferent connectivity, we have identified a medial subdivision of feline area 6 (area 6m) which differs from all surrounding sectors of the frontal lobe in its pattern of inputs. Area 6m is located in the ventral bank of the cruciate sulcus and on the adjacent medial face of the frontal lobe and is partially coextensive with the medial frontal eye field as identified previously in electrophysiological experiments. Area 6m is innervated by axons from visual, association, and oculomotor areas and does not receive projections from somesthetic or somatomotor areas. Cortical sources of input to area 6m include several retinotopically organized extrastriate visual areas (AMLS, ALLS, and PLLS), association areas with strong links to the visual system (area 7, granular insula, posterior ectosylvian gyrus, and cingulate gyrus), and a lateral division of area 6 (area 61) with oculomotor functions. Thalamic afferents of area 6m derive from the paralamellar ventral anterior nucleus, from a dorsolateral division of the mediodorsal nucleus, and from the rostral intralaminar nuclei. The claustrum and the basolateral nucleus of the amygdala project to area 6m. Projections from area 7, the posterior cingulate area, the ventral anterior nucleus, and the mediodorsal nucleus are spatially ordered in a pattern such that parts of area 6 close to the fundus of the cruciate sulcus receive input from neurons positioned anteriorly in the cortical areas, dorsolaterally in the ventral anterior nucleus, and ventrolaterally in the mediodorsal nucleus. Our results indicate that area 6m probably is involved in the voluntary control of gaze and attention rather than in skeletomotor functions.

Afferent Pathways↗

Ectosylvian visual area of the cat: location, retinotopic organization, and connections.

We have mapped out the ectosylvian visual area (EVA) of the cat in a series of single- and multiunit recording studies. EVA occupies 10-20 mm2 of cortex at the posterior end of the horizontal limb of the anterior ectosylvian sulcus. EVA borders on somatosensory cortex anteriorly, auditory cortex posteriorly, and nonresponsive cortex laterally. EVA exhibits limited retinotopic organization, as indicated by the fact that receptive fields shift gradually with tangential travel of the microelectrode through cortex. However, a point-to-point representation of the complete visual hemifield is not present. We have characterized the afferent and efferent connections of EVA by placing retrograde and anterograde tracer deposits in EVA and in other cortical visual areas. The strongest transcortical fiber projection to EVA arises in the lateral suprasylvian visual areas. Area 20, the granular insula, and perirhinal cortex provide additional sparse afferents. The projection from lateral suprasylvian cortex to EVA arises predominantly in layer 3 and terminates in layer 4. EVA projects reciprocally to all cortical areas from which it receives input. The projection from EVA to the lateral suprasylvian areas arises predominantly in layers 5 and 6 and terminates in layer 1. EVA is linked reciprocally to a thalamic zone encompassing the lateromedial-suprageniculate complex and the adjacent medial subdivision of the latero-posterior nucleus. We conclude that EVA is an exclusively visual area confined to the anterior ectosylvian sulcus and bounded by nonvisual cortex. EVA is distinguished from other visual areas by its physical isolation from those areas, by its lack of consistent global retinotopic organization, and by its placement at the end of a chain of areas through which information flows outward from the primary visual cortex.

Animals↗

Cortical and subcortical afferent connections of a posterior division of feline area 7 (area 7p).

Area 7 of the cat, as identified cytoarchitecturally, includes cortex both on the middle suprasylvian gyrus and on the anterior lateral gyrus. The aim of the experiments reported here was to determine whether within this zone there are subdivisions with qualitatively different patterns of afferent connectivity. Deposits of distinguishable retrograde tracers were placed at 29 sites in and around area 7 of 15 cats; cortical and subcortical telencephalic structures were then scanned for retrograde labeling. Our results indicate that cortex on the anterior lateral gyrus, although often included in area 7, is indistinguishable on connectional grounds from adjacent somesthetic cortex (area 5b). Cortex with strong links to visual, oculomotor, and association areas is confined to the middle suprasylvian gyrus and the adjacent lateral bank of the lateral sulcus. We refer to this discrete, connectionally defined zone as posterior area 7 (area 7p). Area 7p receives input from visual areas 19, 20a, 20b, 21a, 21b, AMLS, ALLS, and PLLS; from frontal oculomotor cortex (areas 6m and 6l); and from cortical association areas (posterior cingulate cortex, the granular insula, the posterior ectosylvian gyrus, and posterior area 35). Thalamic projections to area 7p arise from three specific nuclei (pulvinar; nucleus lateralis intermedius, pars caudalis; nucleus ventralis anterior) and from the intralaminar complex (nuclei centralis lateralis, paracentralis and centralis medialis). Neurons in a division of the claustrum immediately beneath the somatosensory and visual zones project to area 7p. Within area 7p, anterior-posterior regional differentiation is present, as indicated by the spatial ordering of projections from cingulate and frontal cortex, the thalamus, and the claustrum. Area 7p, as delineated by connectional analysis in this study, resembles cortex of the primate inferior parietal lobule both in its location relative to other cortical districts and in its pattern of neural connectivity.

Animals↗

Sensory maps in the claustrum of the cat.

The claustrum is a telencephalic cell group (Fig. 1A, B) possessing widespread reciprocal connections with the neocortex. In this regard, it bears a unique and striking resemblance to the thalamus. We have now examined the anatomical ordering of pathways linking the claustrum with sensory areas of the cat neocortex and, in parallel electrophysiological experiments, have studied the functional organization of claustral sensory zones so identified. Our findings indicate that there are discrete visual and somatosensory subdivisions in the claustrum interconnected with the corresponding primary sensory areas of the neocortex and that the respective zones contain orderly retinotopic and somatotopic maps. A third claustral region receiving fibre projections from the auditory cortex in or near area Ep was found to contain neurones responsive to auditory stimulation. We conclude that loops connecting sensory areas of the neocortex with satellite zones in the claustrum contribute to the early processing of exteroceptive information by the forebrain.

Animals↗

Rescaling of the retinal map of visual space during growth of the kitten's eye.

We have measured the angle between the visual axis and the axis projected from the center of the optic disk in 35 cats ranging in age from two weeks to adulthood. Our results show that this angle, a, declines from around 27 degrees in very young kittens to about 16 degrees in adult cats, with most of the change occurring during the first 6 weeks after birth. We interpret this change as reflecting a progressive contraction of the area of object space projected onto the retina. For this to occur, the posterior nodal distance of the eye's optical system must increase by a larger factor than the transverse extent of the retina. This process undoubtedly contributes to maturation of the kitten's visual function, causing a reduction of the size of neuronal receptive fields and an enhancement of spatial resolution.

Age Factors↗

Cortical effects of daily sequential stimulation of right and left eyes in the kitten.

Beginning near the peak of the sensitive period to monocular deprivation, kittens were reared in darkness except for daily sessions during which the left eye was exposed first followed immediately by an equal amount of right eye exposure. The notion was that the sequence of stimulation may be an important determinant in cortical representation of each eye. Although study of single neurons in area 17 showed that nearly all cells were monocular, no systematic imbalance was found in the numbers of units controlled by each eye.

Animals↗

Spatial localization in cats reared with strabismus.

1. The capacity for judging the location of an object relative to the body (egocentric localization) was assessed in cats by measuring the landing position attained when the cat jumped toward a platform viewed from a known distance. 2. Normal cats and kittens land at center of the platform when using one eye or both. In contrast, nine animals tested immediately after tenotomy of the medial rectus muscle of one eye all landed consistently off-center when using the operated eye. The direction of the error was predictable from the assumption that the cat was unaware of the eye's deviation from its natural position. Thus, proprioceptive reafference is not capable, under these conditions, of supporting an accurate awareness of eye position. 3. After initial testing, all cats were maintained in a normal environment with both eyes open and were tested intermittently. Jumps guided by the deviated eye became accurate over a period of weeks in kittens younger than 4 mo. In contrast, behavioral adjustment in older kittens required many months. An adult cat displayed almost no adjustment over a period of 9 mo. 4. Five additional kittens were first tested several months after the onset of strabismus. These animals manifested accurate use of the operated eye from the first trial onward. Therefore, acquisition of accurate use of the deviated eye is not dependent on repeated testing. 5. Two kittens subjected to early exodeviation of one eye displayed a reduced capacity for adjustment when subjected to late exodeviation of the second eye. Thus, changes in neural function resulting from early strabismus (for instance, the loss of binocular connectivity in striate cortex) do not produce persistent behavioral flexibility. 6. In two strabismic kittens with a fully developed compensatory adjustment of monocular egocentric localization, the capacity for judging the relative location of two objects viewed simultaneously through separate eyes was assessed through use of a two-choice visual discrimination paradigm. One animal made predictable systematic errors, while the other exhibited correct judgments. Thus, it appears that a compensatory shift of retinal correspondence may occur in some strabismic kittens, but that such a change is not necessary for accurate use of the deviated eye in monocular visual guidance. 7. A number of observations are described that tend to indicate that cats reared with strabismus continue to use both the deviated and the nondeviated eye for visual guidance under binocular viewing conditions, unlike many human strabismics.

Adaptation, Physiological↗

Eye alignment in kittens.

1. The alignment of the pupillary axes and of the visual axes has been measured in 23 normally reared cats ranging in age from 14 days to adulthood. 2. In agreement with a previous report, we find that pupillary divergence, as measured from photographs, tends to decrease during the first 2 mo of life. 3. The angle between the visual axes of cats of various ages was determined during paralysis by plotting the receptive fields of neurons in cortical area 17, and extrapolation to the angle of alignment of the freely moving animal was accomplished by comparing pupillary photographs taken before and after immobilization. Results obtained by this method reveal that in cats of all ages the visual axes are convergent, and that the average angle of convergence is approximately the same at all ages. 4. We conclude that young kittens may be capable of coordinated binocular vision. Further study will be required to determine whether animals as young as 2 wk are able to align their eyes accurately so as to bring the two retinal images of object space into register. 5. Pupillary divergence decreases during development as a result of changes in the geometry of the eye characterized by a reduction of the angle between the pupillary axis and the visual axis in each eye. This angle changes from around 25 degrees at 14 days to around 16 degrees in adulthood. 6. The role of visual experience in the maintenance of normal eye alignment was investigated by rearing five cats in darkness until the age of 4-7 mo. In three animals, visual axis alignment was within the normal range. The two remaining cats were slightly exotropic. 7. A change occurs during development in the apparent cyclotorsional alignment of the eyes, as determined by measuring the intorsional angle formed by the two slit pupils. This angle increases during the 1st and 2nd mo, assuming a mean value of 14 degrees. In dark-reared cats the increase continues through the 3rd mo, culminating in an abnormally large angle of pupillary intorsion (mean of 24 degrees). The possibility that these changes reflect true shifts in cyclotorsional alignment of the eyes is discussed.

Animals↗

Progressive changes in kitten striate cortex during monocular vision.

Following initial rearing in either total darkness or normal illumination, kittens at different ages were subjected to right-eye closure and various periods of vision through the left eye. After the period of monocular vision, single units in striate cortex were tested for visual responsiveness through each eye. A severe reduction in the proportion of units responsive to the deprived eye occurred over the first few days of monocular vision. Functional abnormalities were variably present after 1 day, marked after 2.5 and 3.5 days, and complete after 10 days. Monocular vision produced very much the same effect on ocular dominance of striate units, provided age and duration of suture were identical, regardless of whether kittens had received prior dark- or light-rearing.

Animals↗