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Corticothalamic connections of the superior temporal sulcus in rhesus monkeys

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Summary

The corticothalamic connections of the superior temporal sulcus (STS) were studied by means of the autoradiographic technique. The results indicate that corticothalamic connections of the STS in general reciprocate thalamocortical connections. The cortex of the upper bank of the STS-multimodal areas TPO and PGa-projects to four major thalamic targets: the pulvinar complex, the mediodorsal nucleus, the limitanssuprageniculate nucleus, as well as intralaminar nuclei. Within the pulvinar complex, the main projections of the upper bank of the STS are directed to the medial pulvinar (PM) nucleus. Rostral upper bank regions tend to project caudally and medially within the PM nucleus, caudal upper bank regions, more laterally and ventrally. The mid-portion of the upper bank tends to occupy the central sector of the PM nucleus. There are also relatively minor projections from upper bank regions to the lateral pulvinar (PL) and oral pulvinar (PO) nuclei. In contrast to the upper bank, the projections from the lower bank are directed primarily to the pulvinar complex, with only minor projections to intralaminar nuclei. The rostral portion of the lower bank projects mainly to caudal and medial regions of the PM nucleus, whereas the caudal lower bank projects predominantly to the lateral PM nucleus, and also to the PL, PO, and inferior pulvinar (PI) nuclei. The mid-portion of the lower bank projects mainly to central and lateral portions of the PM nucleus, and also to the PI and PL nuclei. The rostral depth of the STS projects mainly to the PM nucleus, with only minor connections to the PO, PI, and PL nuclei. The midportion of multimodal area TPO of the upper bank, areas TPO2 and TPO3, projects preferentially to the central sector of the PM nucleus. It is possible that this STS-thalamic connectivity has a role in behavior that is dependent upon more than one sensory modality.

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Abbreviations

AM:

anterior medial nucleus

AS:

arcuate sulcus

AV:

anterior ventral nucleus

BSC:

brachium of the superior colliculus

Cd:

caudate nucleus

Cif:

nucleus centralis inferior

Cim:

nucleus centralis intermedialis

CL:

central lateral nucleus

CM:

centromedian nucleus

CM-Pf:

centromedian-parafascicular nucleus

Cs:

nucleus centralis superior

CS:

central sulcus

CSL:

nucleus centralis lateralis superior

GLd:

dorsal lateral geniculate nucleus

GM:

medial geniculate nucleus

Hb:

habenula

IOS:

inferior occipital sulcus

IPS:

intraparietal sulcus

LD:

lateral dorsal nucleus

LF:

lateral fissure

Li:

limitans nucleus

LP:

lateral posterior nucleus

LS:

lunate sulcus

MD:

mediodorsal nucleus

Pa:

paraventricular nucleus

Pen:

paracentral nucleus

Pf:

parafascicular nucleus

PI:

inferior pulvinar nucleus

PL:

lateral pulvinar nucleus

PM:

medial pulvinar nucleus

PO:

oral pulvinar nucleus

PS:

principal sulcus

Pt:

parataenial nucleus

R:

reticular nucleus

Re:

reuniens nucleus

SG:

suprageniculate nucleus

STN:

subthalamic nucleus

STS:

superior temporal sulcus

THI:

habenulo-interpeduncular tract

VLc:

nucleus ventralis lateralis, pars caudalis

VLm:

nucleus ventralis lateralis, pars medialis

VLo:

nucleus ventralis lateralis, pars oralis

VLps:

nucleus ventralis lateralis, pars postrema

VPI:

ventroposteroinferior nucleus

VPLc:

nucleus ventralis posterior lateralis, pars caudalis

VPLo:

nucleus ventralis posterior lateralis, pars oralis

VPM:

ventroposteromedial nucleus

VPMpc:

ventroposteromedial nucleus, parvocellular portion

X:

nucleus X

References

  • Acuña C, Cudeiro J, González F (1986) Lateral-posterior (LP) and pulvinar unit activity related to intentional upper limb movements directed to spatially separated targets, in behaving Macaca nemestrina monkeys. Rev Neurol (Paris) 142:354–361

    Google Scholar 

  • Acuña C, González F, Dominguez R (1983) Sensorimotor unit activity related to intention in the pulvinar of behaving Cebus apella monkeys. Exp Brain Res 52:411–422

    Google Scholar 

  • Albright TD (1984) Direction and orientation selectivity of neurons in visual area MT of the macaque. J Neurophysiol 52:1106–1130

    Google Scholar 

  • Albright TD (1989) Centrifugal directional bias in the middle temporal visual area (MT) of the macaque. Visual Neurosci 2:177–188

    Google Scholar 

  • Albright TD, Desimone R (1987) Local precision of visuotopic organization in the middle temporal area (MT) of the macaque. Exp Brain Res 65:582–592

    Google Scholar 

  • Albright TD, Desimone R, Gross CG (1984) Columnar organization of directionally sensitive cells in visual area MT of the macaque. J Neurophysiol 51:16–31

    Google Scholar 

  • Ban T (1986) Cortical neurons projecting to the posterior part of the superior temporal sulcus with particular reference to the posterior association area: an HRP study in the monkey. Arch Ital Biol 124:95–109

    Google Scholar 

  • Barnes CL, Pandya DN (1986) Efferent cortical connections of multimodal area TPO of superior temporal gyrus in the rhesus monkey. Soc Neurosci Abstr 12:260

    Google Scholar 

  • Baylis GC, Rolls ET, Leonard CM (1985) Selectivity between faces in the responses of a population of neurons in the cortex in the superior temporal sulcus of the monkey. Brain Res 342:91–102

    Google Scholar 

  • Baylis GC, Rolls ET, Leonard CM (1987) Functional subdivisions of the temporal lobe neocortex. J Neurosci 7:330–342

    Google Scholar 

  • Bender DB (1981) Retinotopic organization of macaque pulvinar. J Neurophysiol 46:672–693

    Google Scholar 

  • Bender DB (1982) Receptive-field properties of neurons in the macaque inferior pulvinar. J Neurophysiol 48:1–17

    Google Scholar 

  • Bender DB (1988) Electrophysiological and behavioral experiments on the primate pulvinar. Progr Brain Res 75:55–65

    Google Scholar 

  • Bender DB, Butter C (1987) Comparison of the effects of superior colliculus and pulvinar lesions on visual search and tachistoscopic pattern discrimination in monkeys. Exp Brain Res 69:140–154

    Google Scholar 

  • Benevento LA, Fallon J, Davis BJ, Rezak M (1977) Auditory-visual interaction in single cells in the cortex of the superior temporal sulcus and the orbital frontal cortex of the macaque monkey. Exp Neurol 57:849–872

    Google Scholar 

  • Benevento LA, Miller J (1981) Visual responses of single neurons in the caudal lateral pulvinar of the macaque monkey. J Neurosci 1:1268–1278

    Google Scholar 

  • Benevento LA, Rezak M (1976) The cortical projections of the inferior pulvinar and adjacent lateral pulvinar in the rhesus monkey (Macaco mulatto): an autoradiographic study. Brain Res 108:1–24

    Google Scholar 

  • Bruce C, Desimone R, Gross CG (1981) Visual properties of neurons in a polysensory area in superior temporal sulcus of the macaque. J Neurophysiol 46:369–384

    Google Scholar 

  • Burton H, Jones EG (1976) The posterior thalamic region and its cortical projection in New World and Old World monkeys. J Comp Neurol 168:249–302

    Google Scholar 

  • Chalupa LM (1977) A review of cat and monkey studies implicating the pulvinar in visual function. Behav Biol 20:149–167

    Google Scholar 

  • Chalupa LM, Coyle RS, Lindsley DB (1976) Effect of pulvinar lesions on visual pattern discrimination in monkeys. J Neurophysiol 39:354–369

    Google Scholar 

  • Cowan WM, Gottlieb DI, Hendrickson AE, Price JL, Woolsey TA (1972) The autoradiographic demonstration of axonal connections in the central nervous system. Brain Res 37:21–51

    Google Scholar 

  • Cudeiro J, González F, Pérez R, Alonso JM, Acuña C (1989) Does the pulvinar-LP complex contribute to motor programming? Brain Res 484:367–370

    Google Scholar 

  • Desimone R, Albright TD, Gross CG, Bruce C (1984) Stimulusselective properties of inferior temporal neurons in the macaque. J Neurosci 4:2051–2062

    Google Scholar 

  • Desimone R, Gross CG (1979) Visual areas in the temporal cortex of the macaque. Brain Res 178:363–380

    Google Scholar 

  • Desimone R, Ungerleider LG (1986) Multiple visual areas in the caudal superior temporal sulcus of the macaque. J Comp Neurol 248:164–189

    Google Scholar 

  • Dürsteler MR, Wurtz RH (1988) Pursuit and optokinetic deficits following chemical lesions of cortical areas MT and MST. J Neurophysiol 60:940–965

    Google Scholar 

  • Dürsteler MR, Wurtz RH, Newsome WT (1987) Directional pursuit deficits following lesions of the foveal representation within the superior temporal sulcus of the macaque monkey. J Neurophysiol 57:1262–1287

    Google Scholar 

  • Erickson RG, Dow BM (1989) Foveal tracking cells in the superior temporal sulcus of the macaque monkey. Exp Brain Res 78:113–131

    Google Scholar 

  • Erickson RG, Dow BM, Snyder AZ (1989) Representation of the fovea in the superior temporal sulcus of the macaque monkey. Exp Brain Res 78:90–112

    Google Scholar 

  • Galaburda AM, Pandya, DN (1983) The intrinsic architectonic and connectional organization of the superior temporal region of the rhesus monkey. J Comp Neurol 221:169–184

    Google Scholar 

  • Gattass R, Gross, CG (1981) Visual topography of striate projection zone (MT) in posterior superior temporal sulcus of the macaque. J Neurophysiol 46:621–638

    Google Scholar 

  • Gattass R, Oswaldo-Cruz E, Sousa APB (1978a) Visuotopic organization of the cebus pulvinar: a double representation of the contralateral hemifield. Brain Res 152:1–16

    Google Scholar 

  • Gattass R, Oswaldo-Cruz E, Sousa APB (1979) Visual receptive fields of units in the pulvinar of cebus monkey. Brain Res 160:413–430

    Google Scholar 

  • Gattass R, Sousa APB, Oswaldo-Cruz E (1978b) Single unit response types in the pulvinar of the cebus monkey to multisensory stimulation. Brain Res 158:75–87

    Google Scholar 

  • Hasselmo ME, Rolls ET, Baylis GC (1989a) The role of expression and identity in the face-selective responses of neurons in the temporal visual cortex of the monkey. Behav Brain Res 32:203–218

    Google Scholar 

  • Hasselmo ME, Rolls ET, Baylis GC, Nalwa V (1989b) Objectcentered encoding by face-selective neurons in the cortex of the superior temporal sulcus of the monkey. Exp Brain Res 75:417–429

    Google Scholar 

  • Heilman KM, Pandya DN, Karol EA, Geschwind N (1971) Auditory inattention. Arch Neurol 24:323–325

    Google Scholar 

  • Hikosaka K, Iwai E, Saito H-A, Tanaka K (1988) Polysensory properties of neurons in the anterior bank of the caudal superior temporal sulcus of the macaque monkey. J Neurophysiol 60:1615–1637

    Google Scholar 

  • Jones EG (1985) The thalamus. Plenum, New York

    Google Scholar 

  • Jones EG, Powell TPS (1970) An anatomical study of converging sensory pathways within the cerebral cortex of the monkey. Brain 93:793–820

    Google Scholar 

  • Kennedy H, Bullier J (1985) A double-labeling investigation of the afferent connectivity to cortical areas V1 and V2 of the macaque monkey. J Neurosci 5:2815–2830

    Google Scholar 

  • Komatsu H, Wurtz RH (1988a) Relation of cortical areas MT and MST to pursuit eye movements. I. Localization and visual properties of neurons. J Neurophysiol 60:580–603

    Google Scholar 

  • Komatsu H, Wurtz RH (1988b) Relation of cortical areas MT and MST to pursuit eye movements. II. Interaction with full-field visual stimulation. J Neurophysiol 60:621–644

    Google Scholar 

  • Komatsu H, Wurtz RH (1989) Modulation of pursuit eye movements by stimulation of cortical areas MT and MST. J Neurophysiol 62:31–47

    Google Scholar 

  • Kuypers HGJM, Szwarcbart MK, Mishkin M, Rosvold HE (1965) Occipitotemporal corticocortical connections in the rhesus monkey. Exp Neurol 11:245–262

    Google Scholar 

  • Leiby CC III, Bender DB, Butter CM (1982) Localization and detection of visual stimuli in monkeys with pulvinar lesions. Exp Brain Res 48:449–454

    Google Scholar 

  • Leichnetz GR (1989) Inferior frontal eye field projections to the pursuit-related dorsolateral pontine nucleus and middle temporal area (MT) in the monkey. Visual Neurosci 3:171–180

    Google Scholar 

  • Logothetis NK, Schall JD (1989) Neuronal correlates of subjective visual perception. Science 245:761–763

    Google Scholar 

  • Luh KE, Butter CM, Buchtel HA (1986) Impairments in orienting to visual stimuli in monkeys following unilateral lesions of the superior temporal polysensory cortex. Neuropsychologia 24:461–470

    Google Scholar 

  • Magariños-Ascone C, Buño W Jr., García-Austt E (1988) Monkey pulvinar units related to motor activity and sensory response. Brain Res 445:30–38

    Google Scholar 

  • Maioli MG, Galletti C, Squatrito S, Battaglini PP, Sanseverino, ER (1984) Projections from the cortex of the superior temporal sulcus to the dorsal lateral geniculate and pregeniculate nuclei in the macaque monkey. Arch Ital Biol 122:301–309

    Google Scholar 

  • Maioli MG, Squatrito S, Galletti C, Battaglini PB, Sanseverino ER (1983) Cortico-cortical connections from the visual region of the superior temporal sulcus to frontal eye field in the macaque. Brain Res 265:294–299

    Google Scholar 

  • Mathers LH, Rapisardi SC (1973) Visual and somatosensory receptive fields of neurons in the squirrel monkey pulvinar. Brain Res 64:65–83

    Google Scholar 

  • Maunsell JHR, Van Essen DC (1983a) The connections of the middle temporal visual area (MT) and their relationship to a cortical hierarchy in the macaque monkey. J Neurosci 3:2563–2586

    Google Scholar 

  • Maunsell JHR, Van Essen DC (1983b) Functional properties of neurons in middle temporal visual area of the macaque monkey. I. Selectivity for stimulus direction, speed, and orientation. J Neurophysiol 49:1127–1147

    Google Scholar 

  • Maunsell JHR, Van Essen DC (1983c) Functional properties of neurons in middle temporal visual area of the macaque monkey. II. Binocular interactions and sensitivity to binocular disparity. J Neurophysiol 49:1148–1167

    Google Scholar 

  • Maunsell JHR, Van Essen DC (1987) Topographic organization of the middle temporal visual area in the macaque monkey: representational biases and the relationship to callosal connections and myeloarchitectonic boundaries. J Comp Neurol 266:535–555

    Google Scholar 

  • Nagel-Leiby S, Bender DB, Butter CM (1984) Effects of kainic acid lesions of the pulvinar on visual discrimination in the monkey. Brain Res 300:295–303

    Google Scholar 

  • Neal JW, Pearson RCA, Powell TPS (1988) The organization of the cortico-cortical connections between the walls of the lower part of the superior temporal sulcus and the inferior parietal lobule in the monkey. Brain Res 438:351–356

    Google Scholar 

  • Newsome WT, Britten KH, Movshon JA (1989) Neuronal correlates of a perceptual decision. Nature 341:52–54

    Google Scholar 

  • Newsome WT, Paré EB (1988) A selective impairment of motion perception following lesions of the middle temporal visual area. J Neurosci 8:2201–2211

    Google Scholar 

  • Newsome WT, Wurtz RH (1988) Probing visual cortical function with discrete chemical lesions. Trends Neurosci 11:394–400

    Google Scholar 

  • Newsome WT, Wurtz RH, Dürsteler MR, Mikami A (1985) Deficits in visual motion processing following ibotenic acid lesions of the middle temporal visual area of the macaque monkey. J Neurosci 5:825–840

    Google Scholar 

  • Olszewski J (1952) The thalamus of the Macaco mulatto. S. Karger, Basel

    Google Scholar 

  • Pandya DN, Rosene DL, Galaburda AM (1986) Thalamic connections of the superior temporal region in rhesus monkey. Soc Neurosci Abstr 12:1368

    Google Scholar 

  • Pandya DN, Sanides F (1973) Architectonic parcellation of the temporal operculum in rhesus monkey, and its projection pattern. Z Anat Entwicklungsgesch 139:127–161

    Google Scholar 

  • Pandya DN, Yeterian EH (1985) Architecture and connections of cortical association areas. In: Peters A, Jones EG (eds) Cerebral cortex, Vol. 4. Association and auditory cortices. Plenum Press, New York, pp 3–61

    Google Scholar 

  • Perrett DI, Mistlin AJ, Chitty AJ (1987) Visual neurones responsive to faces. Trends Neurosci 10:358–364

    Google Scholar 

  • Perrett DI, Rolls ET, Caan W (1982) Visual neurones responsive to faces in the monkey temporal cortex. Exp Brain Res 47:329–342

    Google Scholar 

  • Perrett DI, Smith PAJ, Potter DD, Mistlin AJ, Head AS, Milner AD, Jeeves MA (1984) Neurones responsive to faces in the temporal cortex: studies of functional organization, sensitivity to identity and relation to perception. Human Neurobiol 3:197–208

    Google Scholar 

  • Perrett DI, Smith PAJ, Mistlin AJ, Chitty AJ, Head AS, Potter DD, Broennimann R, Milner AD, Jeeves MA (1985a) Visual analysis of body movements by neurones in the temporal cortex of the macaque monkey: a preliminary report. Behav Brain Res 16:153–170

    Google Scholar 

  • Perrett DI, Smith PAJ, Potter DD, Mistlin AJ, Head AS, Milner AD, Jeeves MA (1985b) Visual cells in the temporal cortex sensitive to face view and gaze direction. Proc R Soc Lond Biol 223:293–317

    Google Scholar 

  • Petersen SE, Robinson DL, Keys W (1985) Pulvinar nuclei of the behaving rhesus monkey: visual responses and their modulation. J Neurophysiol 54:867–886

    Google Scholar 

  • Petersen SE, Robinson DL, Morris JD (1987) Contributions of the pulvinar to visual spatial attention. Neuropsychologia 25:97–105

    Google Scholar 

  • Petrides M, Iversen SD (1978) The effect of selective anterior and posterior association cortex lesions in the monkey on performance of a visual-auditory compound discrimination task. Neuropsychologia 16:527–538

    Google Scholar 

  • Raiguel SE, Lagae L, Gulyas B, Orban G (1989) Response latencies of visual cells in macaque areas V1, V2 and V5. Brain Res 493:155–159

    Google Scholar 

  • Robinson DL, Petersen SE (1985) Responses of pulvinar neurons to real and self-induced movement. Brain Res 338:392–394

    Google Scholar 

  • Robinson DL, Petersen SE, Keys W (1986) Saccade-related and visual activities in the pulvinar nuclei of the behaving rhesus monkey. Exp Brain Res 62:625–634

    Google Scholar 

  • Rockland KS, Pandya DN (1981) Cortical connections of the occipital lobe in the rhesus monkey: interconnections between areas 17, 18, 19 and the superior temporal sulcus. Brain Res 212:249–270

    Google Scholar 

  • Rodman HR, Albright TD (1989) Single-unit analysis of patternmotion selective properties in the middle temporal visual area (MT). Exp Brain Res 75:53–64

    Google Scholar 

  • Rolls, ET (1984) Neurons in the cortex of the temporal lobe and in the amygdala of the monkey with responses selective for faces. Human Neurobiol 3:209–222

    Google Scholar 

  • Rolls ET, Baylis GC (1986) Size and contrast have only small effects on the responses to faces of neurons in the cortex of the superior temporal sulcus of the monkey. Exp Brain Res 65:38–48

    Google Scholar 

  • Rolls ET, Baylis GC, Hasselmo ME (1987) The responses of neurons in the cortex in the superior temporal sulcus of the monkey to band-pass spatial frequency filtered faces. Vision Res 27:311–326

    Google Scholar 

  • Rolls ET, Baylis GC, Hasselmo ME, Nalwa V (1989) The effect of learning on the face selective responses of neurons in the cortex of the superior temporal sulcus of the monkey. Exp Brain Res 76:153–164

    Google Scholar 

  • Rolls ET, Baylis GC, Leonard CM (1985) Role of low and high spatial frequencies in the face-selective responses of neurons in the cortex in the superior temporal sulcus in the monkey. Vision Res 25:1021–1035

    Google Scholar 

  • Rosene DL, Pandya DN (1983) Architectonics and connections of the posterior parahippocampal gyrus in the rhesus monkey. Soc Neurosci Abstr 9:222

    Google Scholar 

  • Saito H, Tanaka K, Isono H, Yasuda M, Mikami A (1989) Directionally sensitive response of cells in the middle temporal area (MT) of the macaque monkey to the movement of equiluminous opponent color stimuli. Exp Brain Res 75:1–14

    Google Scholar 

  • Saito H, Yukie M, Tanaka K, Hikosaka K, Fukuda Y, Iwai E (1986) Integration of direction signals of image motion in the superior temporal sulcus of the macaque monkey. J Neurosci 6:145–157

    Google Scholar 

  • Sanides F (1969) Comparative architectonics of the neocortex of mammals and their evolutionary interpretation. Ann NY Acad Sci 167:404–423

    Google Scholar 

  • Sanides F (1972) Representation in the cerebral cortex and its areal lamination patterns. In: Bourne GF (ed) Structure and function of nervous tissue, Vol. 5. Academic Press, New York, pp 329–453

    Google Scholar 

  • Seltzer B, Pandya DN (1978) Afferent cortical connections and architectonics of the superior temporal sulcus and surrounding cortex in the rhesus monkey. Brain Res 149:1–24

    Google Scholar 

  • Seltzer B, Pandya DN (1989a) Frontal lobe connections of the superior temporal sulcus in the rhesus monkey. J Comp Neurol 281:97–113

    Google Scholar 

  • Seltzer B, Pandya DN (1989b) Intrinsic connections and architectonics of the superior temporal sulcus in the rhesus monkey. J Comp Neurol 290:451–471

    Google Scholar 

  • Shipp S, Zeki S (1989a) The organization of connections between areas V5 and V1 in macaque monkey visual cortex. Europ J Neurosci 1:309–332

    Google Scholar 

  • Shipp S, Zeki S (1989b) The organization of connections between areas V5 and V2 in macaque monkey visual cortex. Europ J Neurosci 1:333–354

    Google Scholar 

  • Shiwa T (1987) Corticocortical projections to the monkey temporal lobe with particular reference to the visual processing pathways. Arch Ital Biol 125:139–154

    Google Scholar 

  • Standage GP, Benevento LA (1983) The organization of connections between the pulvinar and visual area MT in the macaque monkey. Brain Res 262:288–294

    Google Scholar 

  • Tanaka K, Fukada Y, Saito H (1989) Underlying mechanisms of the response specificity of expansion/contraction and rotation cells in the dorsal part of the medial superior temporal area of the macaque monkey. J Neurophysiol 62:642–656

    Google Scholar 

  • Tanaka K, Hikosaka K, Saito H, Yukie M, Fukuda Y, Iwai E (1986) Analysis of local and wide-field movements in the superior temporal visual areas of the macaque monkey. J Neurosci 6:134–144

    Google Scholar 

  • Tanaka K, Saito H (1989) Analysis of motion of the visual field by direction, expansion/contraction, and rotation cells clustered in the dorsal part of the superior temporal area of the macaque monkey. J Neurophysiol 62:626–641

    Google Scholar 

  • Trojanowski JQ, Jacobson S (1975) A combined horseradish peroxidase-autoradiographic investigation of reciprocal conneclions between superior temporal gyrus and pulvinar in squirrel monkey. Brain Res 85:347–353

    Google Scholar 

  • Trojanowski JQ, Jacobson S (1976) Areal and laminar distribution of some pulvinar cortical efferents in rhesus monkey. J Comp Neurol 169:371–392

    Google Scholar 

  • Ungerleider LG, Christensen CA (1977) Pulvinar lesions in monkeys produce abnormal eye movements during visual discrimination learning. Brain Res 136:189–196

    Google Scholar 

  • Ungerleider LG, Christensen CA (1979) Pulvinar lesions in monkeys produce abnormal scanning of a complex visual array. Neuropsychologia 17:493–501

    Google Scholar 

  • Ungerleider LG, Desimone R (1986a) Projections to the superior temporal sulcus from the central and peripheral visual field representations of V1 and V2. J Comp Neurol 248:147–163

    Google Scholar 

  • Ungerleider LG, Desimone R (1986b) Cortical connections of visual area MT in the macaque. J Comp Neurol 248:190–222

    Google Scholar 

  • Ungerleider LG, Desimone R, Galkin TW, Mishkin M (1984) Subcortical projections of area MT in the macaque. J Comp Neurol 223:368–386

    Google Scholar 

  • Ungerleider LG, Mishkin M (1979) The striate projection zone in the superior temporal sulcus of Macaca mulatta: location and topographic organization. J Comp Neurol 188:347–366

    Google Scholar 

  • Van Essen DC, Maunsell JHR (1983) Hierarchical organization and functional streams in the visual cortex. Trends Neurosci 6:370–375

    Google Scholar 

  • Van Essen DC, Maunsell JHR, Bixby JL (1981) The middle temporal visual area in the macaque: myeloarchitecture, connections, functional properties and topographic organization. J Comp Neurol 199:293–326

    Google Scholar 

  • Weber JT, Yin TCT (1984) Subcortical projections of the inferior parietal cortex (area 7) in the stumptail monkey. J Comp Neurol 224:206–230

    Google Scholar 

  • Wilson M, Wilson WA Jr, Remez R (1977) Effects of prestriate, inferotemporal, and superior temporal sulcus lesions on attention and gaze shifts in rhesus monkeys. J Comp Physiol Psychol 91:1261–1271

    Google Scholar 

  • Yeterian EH, Pandya DN (1985) Corticothalamic connections of the posterior parietal cortex in the rhesus monkey. J Comp Neurol 237:408–426

    Google Scholar 

  • Yeterian EH, Pandya DN (1989a) Corticothalamic connections of the superior temporal sulcus in rhesus monkeys. Soc Neurosci Abstr 15:72

    Google Scholar 

  • Yeterian EH, Pandya DN (1989b) Thalamic connections of the cortex of the superior temporal sulcus in the rhesus monkey. J Comp Neurol 282:80–97

    Google Scholar 

  • Yirmiya R, Hocherman S (1987) Auditory- and movement-related neural activity interact in the pulvinar of the behaving rhesus monkey. Brain Res 402:93–102

    Google Scholar 

  • Zeki, SM (1978a) The cortical projections of foveal striate cortex in the rhesus monkey. J Physiol 277:227–244

    Google Scholar 

  • Zeki, SM (1978b) Functional specialization in the visual cortex of the rhesus monkey. Nature 274:423–428

    Google Scholar 

  • Zeki, SM (1978c) Uniformity and diversity of structure and function in rhesus monkey prestriate visual cortex. J Physiol 277:273–290

    Google Scholar 

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Yeterian, E.H., Pandya, D.N. Corticothalamic connections of the superior temporal sulcus in rhesus monkeys. Exp Brain Res 83, 268–284 (1991). https://doi.org/10.1007/BF00231152

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