National Academy of Sciences | 150 Year Anniversary

Questions? Call 800-624-6242

| Items in cart [0]

The National Academies Press

PAPERBACK
price:$51.75
add to cart

Rights & Permissions

topleft topright

(NAS Colloquium) Neuroimaging of Human Brain Function (1998)
National Academy of Sciences (NAS)

Citation Manager

. "The representation of the ipsilateral visual field in human cerebral cortex." (NAS Colloquium) Neuroimaging of Human Brain Function. Washington, DC: The National Academies Press, 1998.

Please select a format:

BibTeX EndNote RefMan


Page
61
bottomleft bottomright

The following HTML text is provided to enhance online readability. Many aspects of typography translate only awkwardly to HTML. Please use the page image as the authoritative form to ensure accuracy.


Colloquium on Neuroimaging of Human Brain Function

FIG. 4. Range of activity produced by stimuli of systematically varied extent in the ipsilateral visual field. Stimuli such as that in Fig. 1A were presented within a range of sector sizes (shown in Fig. 1B) in one representative ipsilateral hemisphere (subject JM). The stimulus was displaced from the vertical meridian by 40° of polar angle in A, 20° in B, 10° in C, and 5° in D (see logos). Visual cortical area borders, revealed in the same hemisphere by tests of contralateral retinotopy, are indicated for comparison. Representations of the contralateral horizontal meridian are indicated by solid lines, and representations of the vertical meridia are indicated by dashed lines. The pseudocolor activity scale bar is as described above, except that MR decreases are not shown, for simplicity. In general, cortical activity increased as the stimulus encroaches progressively closer to the vertical meridian. Within early retinotopic areas, such as the border between V1 and V2 (especially C and D), activity appeared first at the representation of the vertical meridian. Ipsilateral activity was correspondingly lacking at area borders corresponding to the contralateral horizontal meridian, such as the borders between V2/V3 and V2/VP. There were also distinct differences between areas in the degree of ipsilateral activation: across a significant range of stimulus extent (5–20° in this example), areas V3A and V4v showed more widespread ipsilateral activation than immediately adjacent areas V3 and VP. Furthermore, the activity in V3A and V4v extended well beyond the vertical meridian representations of these areas, even though these areas show clear contralateral retinotopy in other tests. The differences in ipsilateral fMRI topography between lower (e.g., V1, V2, and V3/VP) vs. presumably higher-tier (e.g., V3A and V4v) retinotopic areas is consistent with the presence of larger receptive fields in the latter. This evidence for larger receptive fields in V3A/V4v is also consistent with other human fMRI (24) and macaque electrophysiology (40).

9. Desimone, R. & Ungerleider, L.G. (1986) J. Comp. Neurol. 248, 164–189.

10. Tanaka, K. & Saito, H. (1989) J. Neurophysiol. 62, 626–641.

11. Duffy, C.J. & Wurtz, R.H. (1991) J. Neurophysiol. 65, 1329–1345.

12. Raiguel, S., Van Hulle, M.M., Xiao, D.K., Marcar, V.L., Lagae, L. & Orban, G.A. (1997) NeuroReport 8, 2803–2808.

13. Blatt, G.J., Andersen, R.A. & Stoner, G.R. (1990) J. Comp. Neurol. 299, 421–445.

14. Desimone, R., Moran, J., Stein, S.J. & Mishkin, M. (1993) Visual Neurosci. 10, 159–171.

15. Gross, C.G., Rocha-Miranda, C.E. & Bender, D.B. (1972) J. Neurophysiol. 35, 96–111.

16. DeYoe, E.A., Felleman, D.J., Van Essen, D.C. & McClendon, E. (1994) Nature (London) 371, 151–154.

17. Clarke, S. & Miklossy, J. (1990) J. Comp. Neurol. 298, 188–214.

18. Hadjikhani, N., Clarke, S., Van Essen, D.C., Drury, H. & Kraftsik, R. (1994) Eur. J. Neurosci. 7, Suppl., 189 (abstr.).

Page
61
Front Matter (R1-R6)
Contents (R7-R8)
The neuroimaging of human brain function (1-2)
Behind the scenes of functional brain imaging: A historical and physiological perspective (3-10)
Event-related functional MRI: Past, present, and future (11-18)
Event-related brain potentials in the study of visual selective attention (19-25)
Functional and structural mapping of human cerebral cortex: Solutions are in the surfaces (26-33)
Imaging neuroscience: Principles or maps? (34-40)
Spatially independent activity patterns in functional MRI data during the Stroop color-naming task (41-48)
Functional analysis of primary visual cortex (V1) in humans (49-55)
The representation of the ipsilateral visual field in human cerebral cortex (56-62)
On the role of selective attention in visual perception (63-68)
Frontoparietal cortical networks for directing attention and the eye to visual locations: Identical, independent, or overlapping neural systems? (69-76)
Neural components of topographical representation (77-84)
The neural development and organization of letter recognition: Evidence from functional neuroimaging, computational modeling, and behavioral studies (85-90)
The effects of practice on the functional anatomy of task performance (91-98)
The acquisition of skilled motor performance: Fast and slow experience-driven changes in primary motor cortex (99-106)
Rapidly induced auditory plasticity: The ventriloquism aftereffect (107-113)
Components of verbal working memory: Evidence from neuroimaging (114-120)
A neural system for human visual working memory (121-128)
Functional neuroimaging studies of encoding, priming, and explicit memory retrieval (129-136)
Anatomy of word and sentence meaning (137-143)
The role of left prefrontal corex in language and memory (144-151)
Neuroimaging studies of word reading (152-159)
Cerebral organization for langague in deaf and hearing subjects: Biological constraints and effects of experience (160-167)