List of contributors | p. xi |
Cortical mechanisms of vision | p. 1 |
References | p. 4 |
Dorsal stream | p. 7 |
The lateral intraparietal area: a priority map in posterior parietal cortex | p. 9 |
Introduction | p. 9 |
Attention | p. 10 |
Why look at LIP? | p. 11 |
LIP and covert attention | p. 13 |
LIP and overt attention | p. 17 |
Active top-down suppression in LIP | p. 22 |
LIP as a priority map: a unifying role | |
References | p. 28 |
Left-to-right reversal of hemispatial neglect symptoms following adaptation to reversing prisms | p. 35 |
Introduction | p. 35 |
Materials and methods | p. 38 |
Apparatus and procedure | p. 41 |
Data analyses | p. 44 |
Results | p. 44 |
Discussion | p. 46 |
References | p. 48 |
Sensorimotor aspects of reach deficits in optic ataxia | p. 53 |
Introduction | p. 53 |
Classical deficits described in optic ataxia | p. 57 |
Maintaining spatial constancy | p. 61 |
Sensorimotor integration | p. 66 |
Feedback and online movement control | p. 69 |
Clinical implications | p. 73 |
Conclusions | p. 74 |
References | p. 75 |
When what you see isn't where you get: cortical mechanisms of vision for complex action | p. 81 |
The neural control of reaching under increasingly arbitrary conditions: an introduction | p. 81 |
Visuomotor compatibility and visually guided movements | p. 83 |
A (very) brief history of research on nonstandard visuomotor mapping: behavioral and neurophysiological studies | p. 84 |
Cortical mechanisms of visually guided reaching under increasingly dissociated conditions: the basic network | p. 88 |
The effects of sex on skilled movement performance. We mean being male or female | p. 91 |
The effect of healthy aging on dissociated reaching tasks | p. 95 |
The effect of dementia on the performance of dissociated reaching tasks | p. 100 |
Cortical mechanisms for increasingly complex reaching movements: nonhuman primate studies | p. 107 |
Conclusion | p. 110 |
References | p. 111 |
Neural mechanisms of self-movement: perception for navigation and spatial orientation | p. 119 |
Introduction | p. 120 |
Methods | p. 120 |
Results | p. 122 |
Discussion | p. 141 |
References | p. 144 |
Ventral stream | p. 147 |
Differential development of the human ventral stream | p. 149 |
Behavioral investigations of the development of perception | p. 150 |
Developmental neuroimaging is critical for revealing the neural changes underlying the development of perception | p. 152 |
fMRI measurements of the development of the human ventral stream | p. 153 |
Methodological issues in developmental neuroimaging | p. 153 |
No changes in the anatomical size of the fusiform and parahippocampal gyrus | p. 154 |
BOLD-related confounds across age groups | p. 154 |
Face, place and object-selective cortex in children and adults | p. 155 |
Differential development of the human ventral stream | p. 158 |
Expansion of selectivity into adjacent cortex | p. 159 |
No developmental changes in the size of the LOC or the STS face-selective region after age seven | p. 159 |
Correlation between differential cortical development and recognition memory performance | p. 161 |
Implications of the differential development of visual cortex | p. 163 |
Conclusions | p. 164 |
References | p. 165 |
Clarifying the functional neuroanatomy of face perception by single case neuroimaging studies of acquired prosopagnosia | p. 171 |
Introduction | p. 172 |
Neuroimaging studies of face perception in the healthy brain | p. 172 |
Understanding how the human brain processes faces by combining lesion studies and functional neuroimaging | p. 175 |
Conclusions and future directions | p. 197 |
References | p. 199 |
An integrative approach towards understanding the psychological and neural basis of congenital prosopagnosia | p. 209 |
Background | p. 209 |
Behavioral profile of congenital prosopagnosia | p. 212 |
Neural profile of congenital prosopagnosia | p. 215 |
Structural profile of cognitive prosopagnosia | p. 222 |
Concluding remarks | p. 228 |
References | p. 229 |
Object ontology in temporal lobe ensembles | p. 237 |
About ontologies | p. 237 |
The temporal lobe in primates | p. 238 |
Object ontologies in the temporal lobe | p. 239 |
An instantiation of an object ontology: individuals | p. 241 |
An empirical test of featural versus functional representation of individuals in the temporal lobe | p. 242 |
Conclusions | p. 248 |
References | p. 249 |
Frontal cortex | p. 255 |
How the prefrontal cortex is thought to be involved in response suppression | p. 257 |
Functions of the prefrontal cortex | p. 257 |
Examining response suppression using the anti-saccade task | p. 258 |
Top-down and bottom-up visual attention | p. 260 |
Preparatory set | p. 260 |
Internally driven preparatory signals represent rule-dependentactivity | p. 263 |
Visual burst | p. 264 |
Clinical populations | p. 265 |
Neural prosthetics and beyond | p. 266 |
Concluding remarks | p. 267 |
References | p. 267 |
Prefrontal cortex and the neurophysiology of visual knowledge: perception, action, attention, memory, strategies and goals | p. 273 |
Introduction | p. 273 |
Perception versus action | p. 275 |
Attention versus memory | p. 280 |
Strategies versus mappings | p. 284 |
Previous versus future goals | p. 291 |
Prefrontal cortex: polymath or monomaniac | p. 292 |
Epluribus unum | p. 293 |
References | p. 295 |
Saccade target selection in unconstrained visual search | p. 299 |
Introduction | p. 299 |
Automatic responses during visual search | p. 301 |
Visual processing during visual search | p. 304 |
Attentional processing during visual search | p. 310 |
Saccade processing during visual search | p. 312 |
Conclusion | p. 314 |
References | p. 315 |
Oculomotor control of spatial attention | p. 321 |
Introduction | p. 321 |
Spatial attention | p. 322 |
Control of spatial attention | p. 322 |
Frontal eye fields (FEF) | p. 324 |
Anatomy of the frontal eye fields | p. 324 |
Single unit activity | p. 327 |
Lesion studies | p. 327 |
Oculomotor map | p. 328 |
Stimulation | p. 329 |
Rationale | p. 332 |
Attention task | p. 334 |
Distractor effect | p. 335 |
Microstimulation task | p. 336 |
Effects of microstimulation: inside the motor field | p. 341 |
Effects of microstimulation: outside the motor field | p. 341 |
Timing | p. 341 |
Pathways | p. 342 |
Methodology for future studies of spatial attention | p. 343 |
Conclusions | p. 343 |
References | p. 344 |
Neural mechanisms of attentional selection in visual search: evidence from electromagnetic recordings | p. 351 |
Neural mechanisms of feature selection in visual search | p. 352 |
Solving ambiguities of location coding in visual search | p. 357 |
Recurrent processing and the center-surround profile of the spotlight of attention | p. 362 |
Conclusion | p. 365 |
References | p. 366 |
Attention and consciousness | p. 373 |
Two visual systems: separate pathways for perception and action in the human cerebral cortex | p. 375 |
The origins of vision | p. 375 |
Two visual systems | p. 377 |
Different metrics and frames of reference for perception and action | p. 379 |
Perception, action and illusions | p. 380 |
Interactions between the two streams | p. 391 |
Conclusion | p. 392 |
References | p. 393 |
Requirements for conscious visual processing | p. 399 |
Introduction | p. 399 |
Cortical networks for conscious vision | p. 401 |
Neural decisions and generalized rivalry | p. 405 |
Significance of feedback | p. 411 |
The homunculus and the Cartesian Theater | p. 412 |
Discussion | p. 412 |
References | p. 414 |
Author index | p. 419 |
Subject index | p. 441 |
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