The DOI matches its Crossref record; 52 of the 52 references it cites were found in a registry or an index.
The dynamics of visual adaptation to faces.
Open accessAbstract
Several recent demonstrations using visual adaptation have revealed high-level aftereffects for complex patterns including faces. While traditional aftereffects involve perceptual distortion of simple attributes such as orientation or colour that are processed early in the visual cortical hierarchy, face adaptation affects perceived identity and expression, which are thought to be products of higher-order processing. And, unlike most simple aftereffects, those involving faces are robust to changes in scale, position and orientation between the adapting and test stimuli. These differences raise the question of how closely related face aftereffects are to traditional ones. Little is known about the build-up and decay of the face aftereffect, and the similarity of these dynamic processes to traditional aftereffects might provide insight into this relationship. We examined the effect of varying the duration of both the adapting and test stimuli on the magnitude of perceived distortions in face identity. We found that, just as with traditional aftereffects, the identity aftereffect grew logarithmically stronger as a function of adaptation time and exponentially weaker as a function of test duration. Even the subtle aspects of these dynamics, such as the power-law relationship between the adapting and test durations, closely resembled that of other aftereffects. These results were obtained with two different sets of face stimuli that differed greatly in their low-level properties. We postulate that the mechanisms governing these shared dynamics may be dissociable from the responses of feature-selective neurons in the early visual cortex.
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“Interestingly, for unfamiliar faces, as was the case in our experiments, the boundary shifts towards the most distinctive end-point (i.e., the self-face).”
From The other in me: interpersonal multisensory stimulation changes the mental representation of the self (2012) · cites this paper as [50]
In the citing paper
“Second, previous studies (e.g., [50]) used an identification or classification task to determine the perceived categorical boundary between two facial identities in a morphed continuum, and found that the boundary position for faces familiar to the observer does not significantly differ from the physical 50% morph.”
From The other in me: interpersonal multisensory stimulation changes the mental representation of the self (2012) · cites this paper as [50]
Citations
Cites
A morphable model for the synthesis of 3D faces
Blanz, V., & Vetter, T. R. (1999) · ACM SIGGRAPH Conference (SIGGRAPH) · doi:10.1145/311535.311556 · Cited by 4,695
Blakemore, C. B., & Campbell, F. W. (1969) · The Journal of Physiology · doi:10.1113/jphysiol.1969.sp008862 · Cited by 2,032
A Unified Account of the Effects of Distinctiveness, Inversion, and Race in Face Recognition
Valentine, T. (1991) · The Quarterly Journal of Experimental Psychology Section A · doi:10.1080/14640749108400966 · Cited by 1,434
Multistable phenomena: changing views in perception
Leopold, D. A., & Logothetis, N. K. (1999) · Trends in Cognitive Sciences · doi:10.1016/s1364-6613(99)01332-7 · Cited by 980
Self-citationJohansson, G. (1975) · Scientific American · doi:10.1038/scientificamerican0675-76 · Cited by 951
Prototype-referenced shape encoding revealed by high-level aftereffects
Leopold, D. A., O’Toole, A. J., Vetter, T. R., & Blanz, V. (2001) · Nature Neuroscience · doi:10.1038/82947 · Cited by 875
Self-citationAdaptation, after-effect and contrast in the perception of tilted lines. I. Quantitative studies.
Gibson, J. J., & Radner, M. (1937) · Journal of Experimental Psychology · doi:10.1037/h0059826 · Cited by 793
Neural Correlates of Perceptual Rivalry in the Human Brain
Lumer, E. D., Friston, K. J., & Rees, G. E. (1998) · Science · doi:10.1126/science.280.5371.1930 · Cited by 745
(1991) · Comparative Biochemistry and Physiology Part A Physiology · doi:10.1016/0300-9629(91)90509-b · Cited by 678
Adaptation to natural facial categories
Webster, M. A., Kaping, D., Mizokami, Y., & Duhamel, P. (2004) · Nature · doi:10.1038/nature02420 · Cited by 641
Rhodes, G., Jeffery, L., Watson, T., Clifford, C. W. G., & Nakayama, K. (2003) · Psychological Science · doi:10.1046/j.0956-7976.2003.psci_1465.x · Cited by 462
In the Eye of the Beholder: The Science of Face Perception
Bruce, V., & Young, A. W. (1998) · Cited by 453
Figural aftereffects in the perception of faces
Webster, M. A., & MacLin, O. H. (1999) · Psychonomic Bulletin & Review · doi:10.3758/bf03212974 · Cited by 422
Identification and ratings of caricatures: Implications for mental representations of faces
Rhodes, G., Brennan, S. E., & Carey, S. E. (1987) · Cognitive Psychology · doi:10.1016/0010-0285(87)90016-8 · Cited by 409
Anstis, S., Verstraten, F. A. J., & Mather, G. (1998) · Trends in Cognitive Sciences · doi:10.1016/s1364-6613(98)01142-5 · Cited by 409
Size Adaptation: A New Aftereffect
Blakemore, C. B., & Sutton, P. (1969) · Science · doi:10.1126/science.166.3902.245 · Cited by 386
Size invariance in visual object priming.
Biederman, I., & Cooper, E. E. (1992) · Journal of Experimental Psychology Human Perception & Performance · doi:10.1037/0096-1523.18.1.121 · Cited by 366
The Effects of Distinctiveness in Recognising and Classifying Faces
Valentine, T., & Bruce, V. (1986) · Perception · doi:10.1068/p150525 · Cited by 278
Fitting the Mind to the WorldAdaptation and After-Effects in High-Level Vision
Clifford, C. W. G., & Rhodes, G. (2005) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780198529699.001.0001 · Cited by 269
The motion aftereffect: A modern perspective.
Mather, G., Verstraten, F. A. J., & Anstis, S. (1998) · Lincoln Repository (University of Lincoln) · Cited by 248
Gibson, J. J. (1937) · Journal of Experimental Psychology · doi:10.1037/h0057585 · Cited by 230
A theory about the functional role and synaptic mechanism of visual after-effects
Barlow, H. B. (1991) · Vision · doi:10.1017/cbo9780511626197.034 · Cited by 227
Bar, M., & Biederman, I. (1998) · Psychological Science · doi:10.1111/1467-9280.00086 · Cited by 208
The size-tuning of the face-distortion after-effect
Zhao, L., & Chubb, C. F. (2001) · Vision Research · doi:10.1016/s0042-6989(01)00202-4 · Cited by 179
Perception of Faces, Objects, and ScenesAnalytic and Holistic Processes
Peterson, M. A., & Rhodes, G. (2006) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195313659.001.0001 · Cited by 176
Perceptual adaptation: motion parallels orientation
Clifford, C. W. G. (2002) · Trends in Cognitive Sciences · doi:10.1016/s1364-6613(00)01856-8 · Cited by 168
Visual feature-analyzers and aftereffects of tilt and curvature.
Coltheart, M. (1971) · Psychological Review · doi:10.1037/h0030639 · Cited by 167
(1998) · The MIT Press eBooks · doi:10.7551/mitpress/4779.001.0001 · Cited by 142
Pulling Faces: An Investigation of the Face-Distortion Aftereffect
Watson, T., & Clifford, C. W. G. (2003) · Perception · doi:10.1068/p5082 · Cited by 141
Effect of binocular rivalry suppression on the motion aftereffect
Lehmkuhle, S. W., & Fox, R. A. (1975) · Vision Research · doi:10.1016/0042-6989(75)90266-7 · Cited by 130
Orientation illusions and after-effects: Inhibition between channels
Tolhurst, D. J., & Thompson, P. G. (1975) · Vision Research · doi:10.1016/0042-6989(75)90238-2 · Cited by 126
Subjective contours, tilt aftereffects, and visual cortical organization
Paradiso, M. A., Shimojo, S., & Nakayama, K. (1989) · Vision Research · doi:10.1016/0042-6989(89)90066-7 · Cited by 124
Motion Processing in the Macaque: Revisited with Functional Magnetic Resonance Imaging
Tolias, A. S., Smirnakis, S. M., Augath, M. A., Trinath, T., & Logothetis, N. K. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-21-08594.2001 · Cited by 117
Temporal aspects of spatial adaptation. A study of the tilt aftereffect
Magnussen, S. J., & Johnsen, T. (1986) · Vision Research · doi:10.1016/0042-6989(86)90014-3 · Cited by 95
Hershenson, M. (1989) · Perception & Psychophysics · doi:10.3758/bf03210704 · Cited by 74
Short test flashes produce large tilt aftereffects
Wolfe, J. M. (1984) · Vision Research · doi:10.1016/0042-6989(84)90030-0 · Cited by 74
Tilt Aftereffects in a Self-Organizing Model of the Primary Visual Cortex
Bednar, J. A., & Miikkulainen, R. (2000) · Neural Computation · doi:10.1162/089976600300015321 · Cited by 73
Handbook of Perception, vol. V, Seeing
Ikeda, H. (1976) · British Journal of Ophthalmology · doi:10.1136/bjo.60.9.670-b · Cited by 68
The Network of Brain Areas Involved in the Motion Aftereffect
Taylor, J. G., Schmitz, N., Ziemons, K., Grosse-Ruyken, M.-L., Gruber, O., Mueller-Gaertner, H. W., & Shah, N. J. (2000) · NeuroImage · doi:10.1006/nimg.1999.0529 · Cited by 65
Tracking the Decay of the After-Effect of Seen Rotary Movement
Taylor, M. M. (1963) · Perceptual and Motor Skills · doi:10.2466/pms.1963.16.1.119 · Cited by 61
Harris, J. P., & Calvert, J. E. (1989) · Vision Research · doi:10.1016/0042-6989(89)90179-x · Cited by 58
Saturation of the tilt aftereffect
Greenlee, M. W., & Magnussen, S. J. (1987) · Vision Research · doi:10.1016/0042-6989(87)90017-4 · Cited by 53
On Interocular Transfer of Motion Aftereffects
Wade, N. J., Swanston, M. T., & de Weert, C. M. M. (1993) · Perception · doi:10.1068/p221365 · Cited by 50
The After-effect of Seen Motion: The Role of Retinal Stimulation and of Eye Movements
Anstis, S., & Gregory, R. L. (1965) · Quarterly Journal of Experimental Psychology · doi:10.1080/17470216508416428 · Cited by 47
The Effects of Differential Post-Exposure Illumination on the Decay of a Movement After-Effect
Spigel, I. M. (1960) · The Journal of Psychology · doi:10.1080/00223980.1960.9916438 · Cited by 45
Recovery from Adaptation to Moving Gratings
Keck, M. J., & Pentz, B. (1977) · Perception · doi:10.1068/p060719 · Cited by 38
Fatigue and structural change: two consequences of visual pattern adaptation.
Wolfe, J. M., & O'Connell, K. M. (1986) · PubMed · Cited by 36
Linear and rotation motion aftereffects as a function of inspection duration
Hershenson, M. (1993) · Vision Research · doi:10.1016/0042-6989(93)90018-r · Cited by 30
Mechanisms of purely subjective contour tilt aftereffects
van der Zwan, R., & Wenderoth, P. (1995) · Vision Research · doi:10.1016/0042-6989(95)00012-o · Cited by 30
The Magnitude of Figural After-Effects as a Function of the Duration of the Test-Period
Krauskopf, J. (1954) · The American Journal of Psychology · doi:10.2307/1418491 · Cited by 27
Storage of Spatially Specific Threshold Elevation
Thompson, P., & Movshon, J. A. (1978) · Perception · doi:10.1068/p070065 · Cited by 22
Tilt aftereffects generated by bilaterally symmetrical patterns
van der Zwan, Joung, & Latimer, C. R. (2000) · Spatial Vision · doi:10.1163/156856800741045 · Cited by 11
Flagged first, then by citations
Research works printed but not linked: 2
- Blanz V, 1999, Proceedings of SIGGRAPH '99
- Leopold D.A, 2005, Fitting the mind to the world: adaptation and aftereffects in high-level vision
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Little, A. C., Jones, B. C., & DeBruine, L. M. (2011) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2010.0404 · Cited by 1,070
Norm-based face encoding by single neurons in the monkey inferotemporal cortex
Leopold, D. A., Bondar, I. V., & Giese, M. A. (2006) · Nature · doi:10.1038/nature04951 · Cited by 379
Self-citationWebster, M. A. (2015) · Annual Review of Vision Science · doi:10.1146/annurev-vision-082114-035509 · Cited by 330
Webster, M. A. (2011) · Journal of Vision · doi:10.1167/11.5.3 · Cited by 327
Adaptive norm-based coding of facial identity
Rhodes, G., & Jeffery, L. (2006) · Vision Research · doi:10.1016/j.visres.2006.03.002 · Cited by 327
Metadata
- Authors
- Leopold, D. A., Rhodes, G., Müller, K.-M., & Jeffery, L.
- Affiliations
- Max Planck Institute for Biological Cybernetics (DE)
- The University of Western Australia (AU)
- Venue
- Proceedings of the Royal Society B Biological Sciences
- Publisher
- The Royal Society
- Published
- 2005-05-05
- Volume
- 272
- Issue
- 1566
- Pages
- 897-904
- ISSN
- 0080-4649 (ISSN-L)
- 0962-8452
- 1471-2954
- PMC
- PMC1564098
- OpenAlex
- W2121999982
- Cited by
- 255
- References
- 52
- Citations by year
- 2026: 3 · 2025: 3 · 2024: 11 · 2023: 5 · 2022: 9 · 2021: 8 · 2020: 7 · 2019: 9 · 2018: 8 · 2017: 14 · 2016: 15 · 2015: 22 · 2014: 17 · 2013: 20 · 2012: 16
- FWCI
- 5.30
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Proceedings of the Royal Society B Biological Sciences (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- UWA Profiles and Research Repository (UWA) (submittedVersion)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Face Recognition and Perception
- Life Sciences › Neuroscience › Cognitive Neuroscience › Visual perception and processing mechanisms
- Social Sciences › Psychology › Experimental and Cognitive Psychology › Evolutionary Psychology and Human Behavior
- Keywords
- face aftereffects, visual adaptation, adaptation dynamics, adaptation duration, test length, power-law relationship, early visual cortex
- MeSH terms
- Face, Facial Expression, Figural Aftereffect, Humans, Individuality, Models, Neurological, Pattern Recognition, Visual, Photic Stimulation, Time Factors, Visual Cortex
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