Functional subdivisions of the temporal lobe neocortex

In order to gather evidence on functional subdivisions of the temporal lobe neocortex of the primate, the activity of more than 2600 single neurons was recorded in 10 myelo- and cytoarchitecturally defined subdivisions of the cortex in the superior temporal sulcus (STS) and inferior temporal gyrus of the anterior part of the temporal lobe of 5 hemispheres of 3 macaque monkeys. First, convergence of different modalities into each area was investigated. Areas TS and TAa, in the upper part of this region, were found to receive visual as well as auditory inputs. Areas TPO, PGa, and IPa, in the depths of the STS, received visual, auditory, and somatosensory inputs. Areas TEa, TEm, TE3, TE2, and TE1, which extend from the ventral bank of the STS through the inferior temporal gyrus, were primarily unimodal visual areas. Second, of the cells with visual responses, it was found that some neurons in areas TS-IPa could be activated only by moving visual stimuli, whereas the great majority of neurons in areas TEa-TE1 could be activated by stationary visual stimuli. Third, it was found that there were few sharply discriminating visual neurons in areas TS and TAa; of the sharply discriminating visual neurons in other areas, however, neurons that responded primarily to faces were found predominantly in areas TPO, TEa, and TEm (in which they represented 20% of the neurons with visual responses); neurons that were tuned to relatively simple visual stimuli such as sine-wave gratings, color, or simple shapes were relatively common in areas TEa, TEm, and TE3; and neurons that responded only to complex visual stimuli were common in areas IPa, TEa, TEm, and TE3. These findings show inter alia that areas TPO, PGa, and IPa are multimodal, that the inferior temporal gyrus areas are primarily unimodal, that there are areas in the cortex in the anterior and dorsal part of the STS that are specialized for the analysis of moving visual stimuli, that neurons responsive primarily to faces are found predominantly in areas TPO, TEa, and TEm, and that architectural subdivisions of the temporal lobe cortex are related to neuronal response properties.

[1]  Robert R. Sokal,et al.  A statistical method for evaluating systematic relationships , 1958 .

[2]  B. Kintz,et al.  Computational Handbook of Statistics , 1968 .

[3]  D. B. Bender,et al.  Visual properties of neurons in inferotemporal cortex of the Macaque. , 1972, Journal of neurophysiology.

[4]  F. Manning Serial reversal learning by monkeys with inferotemporal or foveal prestriate lesions. , 1972, Physiology & behavior.

[5]  DETECTION OF MASKED PATTERNS IN MONKEYS WITH INFEROTEMPORAL, STRIATE OR DORSOLATERAL FRONTAL LESIONS* , 1972 .

[6]  James P. Egan,et al.  Signal detection theory and ROC analysis , 1975 .

[7]  H. Burton,et al.  Areal differences in the laminar distribution of thalamic afferents in cortical fields of the insular, parietal and temporal regions of primates , 1976, The Journal of comparative neurology.

[8]  G. V. Hoesen,et al.  Temporal neocortical afferent connections to the amygdala in the rhesus monkey , 1976, Brain Research.

[9]  P. Dean,et al.  Effects of inferotemporal lesions on the behavior of monkeys. , 1976, Psychological bulletin.

[10]  E. T. Rolls,et al.  Hypothalamic neuronal responses associated with the sight of food , 1976, Brain Research.

[11]  R. Remez,et al.  Effects of prestriate, inferotemporal, and superior temporal sulcus lesions on attention and gaze shifts in rhesus monkeys. , 1977, Journal of comparative and physiological psychology.

[12]  B. Kintz,et al.  Computational handbook of statistics, 2nd ed. , 1977 .

[13]  D. Pandya,et al.  Afferent cortical connections and architectonics of the superior temporal sulcus and surrounding cortex in the rhesus monkey , 1978, Brain Research.

[14]  Arjun Sahgal,et al.  Categorization and retrieval after selective inferotemporal lesions in monkeys , 1978, Brain Research.

[15]  E. Rolls,et al.  The latency of activation of neurones in the lateral hypothalamus and substantia innominata during feeding in the monkey , 1979, Brain Research.

[16]  E. Rolls,et al.  Visual responses of neurons in the dorsolateral amygdala of the alert monkey , 1979, Experimental Neurology.

[17]  R. E. Passingham,et al.  Cortical and subcortical afferents to the amygdala of the rhesus monkey (Macaca mulatta) , 1980, Brain Research.

[18]  R. Desimone,et al.  Prestriate afferents to inferior temporal cortex: an HRP study , 1980, Brain Research.

[19]  K. Pribram,et al.  A decisional analysis of the effects of inferotemporal lesions in the rhesus monkey. , 1980, Journal of comparative and physiological psychology.

[20]  L. Weiskrantz,et al.  Recency effects and lesion effects in delayed non-matching to randomly baited samples by monkeys , 1980, Brain Research.

[21]  R. Desimone,et al.  Visual properties of neurons in a polysensory area in superior temporal sulcus of the macaque. , 1981, Journal of neurophysiology.

[22]  D. B. Bender,et al.  Backward masking in monkeys after foveal prestriate and inferior temporal cortex lesions , 1981 .

[23]  Mortimer Mishkin,et al.  Evidence for the sequential participation of inferior temporal cortex and amygdala in the acquisition of stimulus-reward associations , 1981, Behavioural Brain Research.

[24]  J. Fuster,et al.  Inferotemporal neurons distinguish and retain behaviorally relevant features of visual stimuli. , 1981, Science.

[25]  John H. R. Maunsell,et al.  The middle temporal visual area in the macaque: Myeloarchitecture, connections, functional properties and topographic organization , 1981, The Journal of comparative neurology.

[26]  A. M. Laursen A lasting impairment in circle-ellipse discrimination after inferotemporal lesions in monkeys , 1982, Behavioural Brain Research.

[27]  W. O. Saxton,et al.  Interactive image processing with an off‐line minicomputer: organization, performance and applications , 1982, Journal of microscopy.

[28]  Elsevier Biomedical Press RESPONSES OF STRIATAL NEURONS IN THE BEHAVING MONKEY. 1. HEAD OF THE CAUDATE NUCLEUS , 1983 .

[29]  R. Desimone,et al.  Shape recognition and inferior temporal neurons. , 1983, Proceedings of the National Academy of Sciences of the United States of America.

[30]  D. Amaral,et al.  Evidence for a direct projection from the superior temporal gyrus to the entorhinal cortex in the monkey , 1983, Brain Research.

[31]  E. Rolls Neurons in the cortex of the temporal lobe and in the amygdala of the monkey with responses selective for faces. , 1984, Human neurobiology.

[32]  Rolls Et Neurons in the cortex of the temporal lobe and in the amygdala of the monkey with responses selective for faces. , 1984 .

[33]  E. Rolls,et al.  Selectivity between faces in the responses of a population of neurons in the cortex in the superior temporal sulcus of the monkey , 1985, Brain Research.

[34]  E. Rolls,et al.  Neurons in the amygdala of the monkey with responses selective for faces , 1985, Behavioural Brain Research.