The DOI matches its Crossref record; 41 of the 41 references it cites were found in a registry or an index.
Heading encoding in the macaque ventral intraparietal area (VIP)
Abstract
We recorded neuronal responses to optic flow stimuli in the ventral intraparietal area (VIP) of two awake macaque monkeys. According to previous studies on optic flow responses in monkey extrastriate cortex we used different stimulus classes: frontoparallel motion, radial stimuli (expansion and contraction) and rotational stimuli (clockwise and counter-clockwise). Seventy-five percent of the cells showed statistically significant responses to one or more of these optic flow stimuli. Shifting the location of the singularity of the optic flow stimuli within the visual field led to a response modulation in almost all cases. For the majority of neurons, this modulatory influence could be approximated in a statistically significant manner by a two-dimensional linear regression. Gradient directions, derived from the regression parameters and indicating the direction of the steepest increase in the responses, were uniformly distributed. At the population level, an unbiased average response for the stimuli with different focus locations was observed. By applying a population code, termed 'isofrequency encoding', we demonstrate the capability of the recorded neuronal ensemble to retrieve the focus location from its population discharge. Responses to expansion and contraction stimuli cannot be predicted based on quantitative data on a neuron's frontoparallel preferred stimulus direction and the location and size of its receptive field. These results, taken together with data on polymodal motion responses in this area, suggest an involvement of area VIP in the analysis and the encoding of heading.
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“Multisensory PPS neurons integrate tactile, visual, and auditory stimuli when presented at a limited distance from the body (Rizzolatti, Fadiga, Fogassi, & Gallese, 1997; Graziano & Cooke, 2006; Bremmer at al, 2002; Makin et al., 2007; Gentile et al., 2011), but not when further away. This limit defines the boundary of PPS”
From Peripersonal space as the space of the bodily self (2015) · cites this paper as Bremmer at al, 2002
Citations
Cites
Perception of the Visual World
(1952) · Archives of Ophthalmology · doi:10.1001/archopht.1952.01700030123016 · Cited by 3,748
Maunsell, J., & van Essen, D. (1983) · The Journal of Neuroscience · doi:10.1523/jneurosci.03-12-02563.1983 · Cited by 1,602
Implantation of magnetic search coils for measurement of eye position: An improved method
Judge, S. J., Richmond, B. J., & Chu, F. C. (1980) · Vision Research · doi:10.1016/0042-6989(80)90128-5 · Cited by 1,530
The organization of the cortical motor system: new concepts
Rizzolatti, G., Luppino, G., & Matelli, M. (1998) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/s0013-4694(98)00022-4 · Cited by 1,127
Duffy, C. J., & Wurtz, R. H. (1991) · Journal of Neurophysiology · doi:10.1152/jn.1991.65.6.1329 · Cited by 887
Tanaka, K., Hikosaka, K., Saito, H., Yukie, M., Fukada, Y., & Iwai, E. (1986) · Journal of Neuroscience · doi:10.1523/jneurosci.06-01-00134.1986 · Cited by 841
Ventral intraparietal area of the macaque: congruent visual and somatic response properties
Duhamel, J.-R., Colby, C. L., & Goldberg, M. E. (1998) · Journal of Neurophysiology · doi:10.1152/jn.1998.79.1.126 · Cited by 789
The perception of the visual world.
Boring, E. G. (1951) · Psychological Bulletin · doi:10.1037/h0051570 · Cited by 780
Ventral intraparietal area of the macaque: Anatomic location and visual response properties
Colby, C. L., Duhamel, J. R., & Goldberg, M. E. (1993) · Journal of Neurophysiology · doi:10.1152/jn.1993.69.3.902 · Cited by 701
Tanaka, K., & Saito, H. (1989) · Journal of Neurophysiology · doi:10.1152/jn.1989.62.3.626 · Cited by 692
Research works printed but not linked: 7
- Bremmer F., 1997, Encoding of spatial information in monkey visual cortical areas MT and MST, Soc. Neurosci. Abstr., 23, 459
- Bremmer F., 1995, Supramodal encoding of movement space in the ventral intraparietal area of macaque monkeys, Soc. Neurosci. Abstr., 21, 282.
- Bremmer F., 1999, Representation of near extrapersonal space in the macaque ventral intraparietal area (VIP), Soc. Neurosci. Abstr., 25, 1164.
- Duhamel J.‐R., 1997, Encoding of heading direction during simulated self‐motion in the macaque ventral intraparietal area (VIP), Soc. Neurosci. Abstr., 23, 1545
- Graf W., 1996, Visual–vestibular interaction in the ventral intraparietal area of macaque monkeys, Soc. Neurosci. Abstr., 22, 1692
- Klam F., 1998, Vestibular response dynamics in macaque posterior parietal cortex neurons, Soc. Neurosci. Abstr., 24, 601.1
- Schlack A., 2000, Auditory responsiveness in the macaque ventral intraparietal area (VIP), Soc. Neurosc. Abstr., 26, 1064.
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Hervais‐Adelman, A., Legrand, L. B., Zhan, M., Tamietto, M., de Gelder, B., & Pegna, A. J. (2015) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2015.00051 · Cited by 26
Marco, S. D., Fattori, P., Galati, G., Galletti, C., Lappe, M., Maltempo, T., Serra, C., Sulpizio, V., & Pitzalis, S. (2021) · Cortex · doi:10.1016/j.cortex.2020.12.021 · Cited by 25
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Strong, S., Silson, E. H., Gouws, A. D., Morland, A. B., & McKeefry, D. J. (2017) · Journal of Neurophysiology · doi:10.1152/jn.00031.2017 · Cited by 15
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Metadata
- Authors
- Bremmer, F., Duhamel, J., Ben Hamed, S., & Graf, W.
- Affiliations
- Centre National de la Recherche Scientifique (FR)
- Corresponding author
- Bremmer, Frank
- Venue
- European Journal of Neuroscience
- Publisher
- Wiley
- Published
- 2002-10
- Volume
- 16
- Issue
- 8
- Pages
- 1554-1568
- ISSN
- 0953-816X (ISSN-L)
- 1460-9568
- OpenAlex
- W2086569041
- Cited by
- 232
- References
- 41
- Citations by year
- 2026: 6 · 2025: 9 · 2024: 9 · 2023: 5 · 2022: 8 · 2021: 15 · 2020: 7 · 2019: 6 · 2018: 11 · 2017: 15 · 2016: 12 · 2015: 10 · 2014: 12 · 2013: 13 · 2012: 8
- FWCI
- 4.51
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- European Journal of Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- Funders
- European Commission
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Visual perception and processing mechanisms
- Social Sciences › Psychology › Experimental and Cognitive Psychology › Multisensory perception and integration
- Life Sciences › Neuroscience › Neurology › Vestibular and auditory disorders
- Keywords
- ventral intraparietal area, optical flow, macaque, population coding, rotational motion, receptive fields, extrastriate cortex
- MeSH terms
- Action Potentials, Animals, Female, Macaca fascicularis, Macaca mulatta, Motion Perception, Neurons, Orientation, Parietal Lobe, Photic Stimulation, Space Perception, Visual Cortex, Visual Fields
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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