U.S. flag

An official website of the United States government

The .gov means it’s official. Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

The site is secure. The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

  • Publications
  • Account settings
  • My Bibliography
  • Collections
  • Citation manager

Save citation to file

Email citation, add to collections.

  • Create a new collection
  • Add to an existing collection

Add to My Bibliography

Your saved search, create a file for external citation management software, your rss feed.

  • Search in PubMed
  • Search in NLM Catalog
  • Add to Search

A century of Gestalt psychology in visual perception: I. Perceptual grouping and figure-ground organization

Affiliation.

  • 1 University of Leuven (KU Leuven), Laboratory of Experimental Psychology, Tiensestraat 102, Box 3711, BE-3000 Leuven, Belgium. [email protected]
  • PMID: 22845751
  • PMCID: PMC3482144
  • DOI: 10.1037/a0029333

In 1912, Max Wertheimer published his paper on phi motion, widely recognized as the start of Gestalt psychology. Because of its continued relevance in modern psychology, this centennial anniversary is an excellent opportunity to take stock of what Gestalt psychology has offered and how it has changed since its inception. We first introduce the key findings and ideas in the Berlin school of Gestalt psychology, and then briefly sketch its development, rise, and fall. Next, we discuss its empirical and conceptual problems, and indicate how they are addressed in contemporary research on perceptual grouping and figure-ground organization. In particular, we review the principles of grouping, both classical (e.g., proximity, similarity, common fate, good continuation, closure, symmetry, parallelism) and new (e.g., synchrony, common region, element and uniform connectedness), and their role in contour integration and completion. We then review classic and new image-based principles of figure-ground organization, how it is influenced by past experience and attention, and how it relates to shape and depth perception. After an integrated review of the neural mechanisms involved in contour grouping, border ownership, and figure-ground perception, we conclude by evaluating what modern vision science has offered compared to traditional Gestalt psychology, whether we can speak of a Gestalt revival, and where the remaining limitations and challenges lie. A better integration of this research tradition with the rest of vision science requires further progress regarding the conceptual and theoretical foundations of the Gestalt approach, which is the focus of a second review article.

PubMed Disclaimer

Illustration of several grouping principles…

Illustration of several grouping principles (adapted from Palmer, 2002a).

(A) Defining features of a…

(A) Defining features of a dot lattice stimulus. (B) Two-dimensional space and nomenclature…

Two dimotif rectangular dot lattices…

Two dimotif rectangular dot lattices with | b | | a | =…

Two grouping indifference curves. The…

Two grouping indifference curves. The abscissa, δ a , represents the difference in…

The pure distance law (adapted…

The pure distance law (adapted from Kubovy et al., 1998, with permission).

The conjoined effects of proximity…

The conjoined effects of proximity and similarity are additive. The dashed lines in…

formula image

(A) The affinity function. (B)…

(A) The affinity function. (B) The objecthood functions.

A six-stroke motion lattice. (A)…

A six-stroke motion lattice. (A) The successive frames are superimposed in space. Gray…

Object boundaries project to the…

Object boundaries project to the image as fragmented contours, due to occlusions (dashed…

Example of stimuli devised by…

Example of stimuli devised by Field et al. (1993) to probe the role…

Models of good continuation. (A)…

Models of good continuation. (A) Cocircularity support neighborhood (adapted from Parent & Zucker,…

(A) Amodal completion of the…

(A) Amodal completion of the black shape behind the gray shape. (B) A…

Two curved fragments are seen…

Two curved fragments are seen to complete amodally behind the gray rectangle in…

(A) Measuring extrapolation of curvature…

(A) Measuring extrapolation of curvature by (B) asking observers to position and orient…

Contour geometry depends on surface…

Contour geometry depends on surface geometry. The same curved contour segment (A) can…

Example of a display used…

Example of a display used in classic tests of whether or not convexity…

(A–B) Sample stimuli used by…

(A–B) Sample stimuli used by Peterson et al. (1991). The configural factors of…

Sample displays used by Driver…

Sample displays used by Driver and Baylis (1996), adapted with permission. (A). Study…

When a wiggly curved line…

When a wiggly curved line is drawn on a circular disc, the two…

The role of part salience…

The role of part salience in figure-ground organization (adapted from Hoffman & Singh,…

In a configuration with four…

In a configuration with four black pacmen, an illusory white square emerges in…

(a) A quasi-random collection of…

(a) A quasi-random collection of quasi-random shapes. (b) The same shapes as in…

The isolated square (a) and…

The isolated square (a) and the squares with rounded corners (b) appear as…

Similar articles

  • An overview of quantitative approaches in Gestalt perception. Jäkel F, Singh M, Wichmann FA, Herzog MH. Jäkel F, et al. Vision Res. 2016 Sep;126:3-8. doi: 10.1016/j.visres.2016.06.004. Epub 2016 Jul 4. Vision Res. 2016. PMID: 27353224 Review.
  • Subliminal Gestalt grouping: evidence of perceptual grouping by proximity and similarity in absence of conscious perception. Montoro PR, Luna D, Ortells JJ. Montoro PR, et al. Conscious Cogn. 2014 Apr;25:1-8. doi: 10.1016/j.concog.2014.01.004. Epub 2014 Feb 8. Conscious Cogn. 2014. PMID: 24518805
  • A century of Gestalt psychology in visual perception: II. Conceptual and theoretical foundations. Wagemans J, Feldman J, Gepshtein S, Kimchi R, Pomerantz JR, van der Helm PA, van Leeuwen C. Wagemans J, et al. Psychol Bull. 2012 Nov;138(6):1218-52. doi: 10.1037/a0029334. Epub 2012 Jul 30. Psychol Bull. 2012. PMID: 22845750 Free PMC article. Review.
  • To what extent do Gestalt grouping principles influence tactile perception? Gallace A, Spence C. Gallace A, et al. Psychol Bull. 2011 Jul;137(4):538-61. doi: 10.1037/a0022335. Psychol Bull. 2011. PMID: 21574680 Review.
  • Gestalt theory: implications for radiology education. Koontz NA, Gunderman RB. Koontz NA, et al. AJR Am J Roentgenol. 2008 May;190(5):1156-60. doi: 10.2214/AJR.07.3268. AJR Am J Roentgenol. 2008. PMID: 18430824 Review.
  • Investigation of preference for local and global processing of Capuchin-monkeys (Sapajus spp.) in shape discrimination of mosaic arrangements. Mendes F, Brino ALF, Goulart PRK, Galvão OF, Ventura DSF, Miquilini L, Brito FADC, Souza GS. Mendes F, et al. PLoS One. 2024 May 29;19(5):e0303562. doi: 10.1371/journal.pone.0303562. eCollection 2024. PLoS One. 2024. PMID: 38809944 Free PMC article.
  • Qualitative Exploration of Anesthesia Providers' Perceptions Regarding Philips Visual Patient Avatar in Clinical Practice. Hunn CA, Lunkiewicz J, Noethiger CB, Tscholl DW, Gasciauskaite G. Hunn CA, et al. Bioengineering (Basel). 2024 Mar 27;11(4):323. doi: 10.3390/bioengineering11040323. Bioengineering (Basel). 2024. PMID: 38671745 Free PMC article.
  • The Role of Uniform Textures in Making Texture Elements Visible in the Visual Periphery. Bertamini M, Oletto CM, Contemori G. Bertamini M, et al. Open Mind (Camb). 2024 Apr 3;8:462-482. doi: 10.1162/opmi_a_00136. eCollection 2024. Open Mind (Camb). 2024. PMID: 38665546 Free PMC article.
  • Perceptual Resolution of Ambiguity: Can Tuned, Divisive Normalization Account for both Interocular Similarity Grouping and Difference Enhancement. Peiso JR, Palmer SE, Shevell SK. Peiso JR, et al. bioRxiv [Preprint]. 2024 Apr 2:2024.04.01.587646. doi: 10.1101/2024.04.01.587646. bioRxiv. 2024. PMID: 38617235 Free PMC article. Preprint.
  • The dynamics of experiencing Gestalt and Aha in cubist art: pupil responses and art evaluations show a complex interplay of task, stimuli content, and time course. Spee BTM, Arato J, Mikuni J, Tran US, Pelowski M, Leder H. Spee BTM, et al. Front Psychol. 2024 Mar 13;15:1192565. doi: 10.3389/fpsyg.2024.1192565. eCollection 2024. Front Psychol. 2024. PMID: 38544509 Free PMC article.
  • Alais D, Blake R, Lee SH. Visual features that vary together over time group together over space. Nature Neuroscience. 1998;1:160–164. - PubMed
  • Alexander DM, van Leeuwen C. Mapping of contextual modulation in the population response of primary visual cortex. Cognitive Neurodynamics. 2010;4:1–24. - PMC - PubMed
  • Allman J, Miezin F, McGuinness E. Stimulus-specific responses from beyond the classical receptive field: Neurophysiological mechanisms for local-global comparisons in visual neurons. Annual Review of Neuroscience. 1985;8:407–430. - PubMed
  • Altmann CF, Bülthoff HH, Kourtzi Z. Perceptual organization of local elements into global shapes in the human visual cortex. Current Biology. 2003;13:342–349. - PubMed
  • Anderson BL. The demise of the identity hypothesis and the insufficiency and nonnecessity of contour relatability in predicting object interpolation: Comment on Kellman, Garrigan, and Shipley (2005) Psychological Review. 2007;114:470–487. - PubMed

Publication types

  • Search in MeSH

Related information

Grants and funding.

  • R01 EY021494/EY/NEI NIH HHS/United States
  • R01 EY016281/EY/NEI NIH HHS/United States
  • EY16281/EY/NEI NIH HHS/United States
  • R01 EY002966/EY/NEI NIH HHS/United States
  • EY02966/EY/NEI NIH HHS/United States
  • EY021494/EY/NEI NIH HHS/United States

LinkOut - more resources

Full text sources.

  • American Psychological Association
  • Europe PubMed Central
  • Ovid Technologies, Inc.
  • PubMed Central

Other Literature Sources

  • The Lens - Patent Citations

Miscellaneous

  • NCI CPTAC Assay Portal
  • Citation Manager

NCBI Literature Resources

MeSH PMC Bookshelf Disclaimer

The PubMed wordmark and PubMed logo are registered trademarks of the U.S. Department of Health and Human Services (HHS). Unauthorized use of these marks is strictly prohibited.

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • View all journals
  • Explore content
  • About the journal
  • Publish with us
  • Sign up for alerts
  • Review Article
  • Published: 05 August 2019

The human imagination: the cognitive neuroscience of visual mental imagery

  • Joel Pearson   ORCID: orcid.org/0000-0003-3704-5037 1  

Nature Reviews Neuroscience volume  20 ,  pages 624–634 ( 2019 ) Cite this article

35k Accesses

291 Citations

218 Altmetric

Metrics details

  • Object vision
  • Sensory systems
  • Working memory

Mental imagery can be advantageous, unnecessary and even clinically disruptive. With methodological constraints now overcome, research has shown that visual imagery involves a network of brain areas from the frontal cortex to sensory areas, overlapping with the default mode network, and can function much like a weak version of afferent perception. Imagery vividness and strength range from completely absent (aphantasia) to photo-like (hyperphantasia). Both the anatomy and function of the primary visual cortex are related to visual imagery. The use of imagery as a tool has been linked to many compound cognitive processes and imagery plays both symptomatic and mechanistic roles in neurological and mental disorders and treatments.

This is a preview of subscription content, access via your institution

Access options

Access Nature and 54 other Nature Portfolio journals

Get Nature+, our best-value online-access subscription

24,99 € / 30 days

cancel any time

Subscribe to this journal

Receive 12 print issues and online access

176,64 € per year

only 14,72 € per issue

Buy this article

  • Purchase on Springer Link
  • Instant access to full article PDF

Prices may be subject to local taxes which are calculated during checkout

visual perception psychology research paper

Similar content being viewed by others

visual perception psychology research paper

Early-stage visual perception impairment in schizophrenia, bottom-up and back again

visual perception psychology research paper

A cognitive profile of multi-sensory imagery, memory and dreaming in aphantasia

visual perception psychology research paper

Between-subject variability in the influence of mental imagery on conscious perception

Zeman, A., Dewar, M. & Della Sala, S. Lives without imagery — congenital aphantasia. Cortex 73 , 378–380 (2015). This article documents and coins the term aphantasia, described as the complete lack of visual imagery ability .

Article   PubMed   Google Scholar  

Pearson, J. & Westbrook, F. Phantom perception: voluntary and involuntary non-retinal vision. Trends Cogn. Sci. 19 , 278–284 (2015). This opinion paper proposes a unifying framework for both voluntary and involuntary imagery .

Pearson, J., Naselaris, T., Holmes, E. A. & Kosslyn, S. M. Mental imagery: functional mechanisms and clinical applications. Trends Cogn. Sci. 19 , 590–602 (2015).

Article   PubMed   PubMed Central   Google Scholar  

Egeth, H. E. & Yantis, S. Visual attention: control, representation, and time course. Annu. Rev. Psychol. 48 , 269–297 (1997).

Article   CAS   PubMed   Google Scholar  

Dijkstra, N., Zeidman, P., Ondobaka, S., Gerven, M. A. J. & Friston, K. Distinct top-down and bottom-up brain connectivity during visual perception and imagery. Sci. Rep. 7 , 5677 (2017).

Article   CAS   PubMed   PubMed Central   Google Scholar  

Dentico, D. et al. Reversal of cortical information flow during visual imagery as compared to visual perception. Neuroimage 100 , 237–243 (2014).

Schlegel, A. et al. Network structure and dynamics of the mental workspace. Proc. Natl Acad. Sci. USA 110 , 16277–16282 (2013).

Ranganath, C. & D’Esposito, M. Directing the mind’s eye: prefrontal, inferior and medial temporal mechanisms for visual working memory. Curr. Opin. Neurobiol. 15 , 175–182 (2005).

Yomogida, Y. Mental visual synthesis is originated in the fronto-temporal network of the left hemisphere. Cereb. Cortex 14 , 1376–1383 (2004).

Ishai, A., Ungerleider, L. G. & Haxby, J. V. Distributed neural systems for the generation of visual images. Neuron 28 , 979–990 (2000).

Goebel, R., Khorram-Sefat, D., Muckli, L., Hacker, H. & Singer, W. The constructive nature of vision: direct evidence from functional magnetic resonance imaging studies of apparent motion and motion imagery. Eur. J. Neurosci. 10 , 1563–1573 (1998).

Mellet, E. et al. Functional anatomy of spatial mental imagery generated from verbal instructions. J. Neurosci. 16 , 6504–6512 (1996).

O’Craven, K. M. & Kanwisher, N. Mental imagery of faces and places activates corresponding stimulus- specific brain regions. J. Cogn. Neurosci. 12 , 1013–1023 (2000).

Kosslyn, S. M., Ganis, G. & Thompson, W. L. Neural foundations of imagery. Nat. Rev. Neurosci. 2 , 635–642 (2001).

Hassabis, D., Kumaran, D. & Maguire, E. A. Using imagination to understand the neural basis of episodic memory. J. Neurosci. 27 , 14365–14374 (2007).

Bird, C. M., Capponi, C., King, J. A., Doeller, C. F. & Burgess, N. Establishing the boundaries: the hippocampal contribution to imagining scenes. J. Neurosci. 30 , 11688–11695 (2010).

Hassabis, D., Kumaran, D., Vann, S. D. & Maguire, E. A. Patients with hippocampal amnesia cannot imagine new experiences. Proc. Natl Acad. Sci. USA 104 , 1726–1731 (2007).

Kreiman, G., Koch, C. & Fried, I. Imagery neurons in the human brain. Nature 408 , 357–361 (2000).

Maguire, E. A., Vargha-Khadem, F. & Hassabis, D. Imagining fictitious and future experiences: evidence from developmental amnesia. Neuropsychologia 48 , 3187–3192 (2010).

Kim, S. et al. Sparing of spatial mental imagery in patients with hippocampal lesions. Learn. Mem. 20 , 657–663 (2013).

Pearson, J. & Kosslyn, S. M. The heterogeneity of mental representation: ending the imagery debate. Proc. Natl Acad. Sci. USA 112 , 10089–10092 (2015). This paper proposes an end to the ‘imagery debate’ based on the discussed evidence that imagery can be represented in the brain in a depictive manner .

D’Esposito, M. et al. A functional MRI study of mental image generation. Neuropsychologia 35 , 725–730 (1997).

Knauff, M., Kassubek, J., Mulack, T. & Greenlee, M. W. Cortical activation evoked by visual mental imagery as measured by fMRI. Neuroreport 11 , 3957–3962 (2000).

Trojano, L. et al. Matching two imagined clocks: the functional anatomy of spatial analysis in the absence of visual stimulation. Cereb. Cortex 10 , 473–481 (2000).

Wheeler, M. E., Petersen, S. E. & Buckner, R. L. Memory’s echo: vivid remembering reactivates sensory-specific cortex. Proc. Natl Acad. Sci. USA 97 , 11125 (2000).

Formisano, E. et al. Tracking the mind’s image in the brain I: time-resolved fMRI during visuospatial mental imagery. Neuron 35 , 185–194 (2002).

Sack, A. T. et al. Tracking the mind’s image in the brain II: transcranial magnetic stimulation reveals parietal asymmetry in visuospatial imagery. Neuron 35 , 195–204 (2002).

Le Bihan, D. et al. Activation of human primary visual cortex during visual recall: a magnetic resonance imaging study. Proc. Natl Acad. Sci. USA 90 , 11802–11805 (1993).

Sabbah, P. et al. Functional magnetic resonance imaging at 1.5T during sensorimotor and cognitive task. Eur. Neurol. 35 , 131–136 (1995).

Chen, W. et al. Human primary visual cortex and lateral geniculate nucleus activation during visual imagery. Neuroreport 9 , 3669–3674 (1998).

Ishai, A. Visual imagery of famous faces: effects of memory and attention revealed by fMRI. Neuroimage 17 , 1729–1741 (2002).

Ganis, G., Thompson, W. L. & Kosslyn, S. M. Brain areas underlying visual mental imagery and visual perception: an fMRI study. Cogn. Brain Res. 20 , 226–241 (2004).

Article   Google Scholar  

Klein, I., Paradis, A. L., Poline, J. B., Kossly, S. M. & Le Bihan, D. Transient activity in the human calcarine cortex during visual-mental imagery: an event-related fMRI study. J. Cogn. Neurosci. 12 (Suppl. 2), 15–23 (2000).

Lambert, S., Sampaio, E., Scheiber, C. & Mauss, Y. Neural substrates of animal mental imagery: calcarine sulcus and dorsal pathway involvement — an fMRI study. Brain Res. 924 , 176–183 (2002).

Cui, X., Jeter, C. B., Yang, D., Montague, P. R. & Eagleman, D. M. Vividness of mental imagery: individual variability can be measured objectively. Vision Res. 47 , 474–478 (2007).

Amedi, A., Malach, R. & Pascual-Leone, A. Negative BOLD differentiates visual imagery and perception. Neuron 48 , 859–872 (2005).

Reddy, L., Tsuchiya, N. & Serre, T. Reading the mind’s eye: decoding category information during mental imagery. Neuroimage 50 , 818–825 (2010).

Dijkstra, N., Bosch, S. E. & van Gerven, M. A. J. Vividness of visual imagery depends on the neural overlap with perception in visual areas. J. Neurosci. 37 , 1367–1373 (2017).

Kosslyn, S. M. & Thompson, W. L. When is early visual cortex activated during visual mental imagery? Psychol. Bull. 129 , 723–746 (2003).

Albers, A. M., Kok, P., Toni, I., Dijkerman, H. C. & de Lange, F. P. Shared representations for working memory and mental imagery in early visual cortex. Curr. Biol. 23 , 1427–1431 (2013). This paper shows that both imagery and visual working memory can be decoded in the brain based on training on either, showing evidence of a common brain representation .

Koenig-Robert, R. & Pearson, J. Decoding the contents and strength of imagery before volitional engagement. Sci. Rep. 9 , 3504 (2019). This paper shows that the content and vividness of a mental image can be decoded in the brain up to 11 seconds before an individual decides which pattern to imagine .

Article   PubMed   PubMed Central   CAS   Google Scholar  

Naselaris, T., Olman, C. A., Stansbury, D. E., Ugurbil, K. & Gallant, J. L. A voxel-wise encoding model for early visual areas decodes mental images of remembered scenes. Neuroimage 105 , 215–228 (2015). This study shows that mental imagery content can be decoded in the early visual cortex when the decoding model is based on depictive perceptual features .

Fox, M. D. et al. The human brain is intrinsically organized into dynamic, anticorrelated functional networks. Proc. Natl Acad. Sci. USA 102 , 9673–9678 (2005).

Smith, S. M. et al. Correspondence of the brain’s functional architecture during activation and rest. Proc. Natl Acad. Sci. USA 106 , 13040–13045 (2009).

Østby, Y. et al. Mental time travel and default-mode network functional connectivity in the developing brain. Proc. Natl Acad. Sci. USA 109 , 16800–16804 (2012).

Andrews-Hanna, J. R., Reidler, J. S., Sepulcre, J., Poulin, R. & Buckner, R. L. Functional-anatomic fractionation of the brain’s default network. Neuron 65 , 550–562 (2010).

Hassabis, D. & Maguire, E. A. Deconstructing episodic memory with construction. Trends Cogn. Sci. 11 , 299–306 (2007).

Gerlach, K. D., Spreng, R. N., Gilmore, A. W. & Schacter, D. L. Solving future problems: default network and executive activity associated with goal-directed mental simulations. Neuroimage 55 , 1816–1824 (2011).

Levine, D. N., Warach, J. & Farah, M. Two visual systems in mental imagery. Neurology 35 , 1010 (1985).

Keogh, R. & Pearson, J. The blind mind: no sensory visual imagery in aphantasia. Cortex 105 , 53–60 (2017).

Sakai, K. & Miyashita, Y. Neural organization for the long-term memory of paired associates. Nature 354 , 152–155 (1991).

Messinger, A., Squire, L. R., Zola, S. M. & Albright, T. D. Neuronal representations of stimulus associations develop in the temporal lobe during learning. Proc. Natl Acad. Sci. USA 98 , 12239–12244 (2001).

Schlack, A. & Albright, T. D. Remembering visual motion: neural correlates of associative plasticity and motion recall in cortical area MT. Neuron 53 , 881–890 (2007).

Bannert, M. M. & Bartels, A. Decoding the yellow of a gray banana. Curr. Biol. 23 , 2268–2272 (2013).

Hansen, T., Olkkonen, M., Walter, S. & Gegenfurtner, K. R. Memory modulates color appearance. Nat. Neurosci. 9 , 1367–1368 (2006).

Meng, M., Remus, D. A. & Tong, F. Filling-in of visual phantoms in the human brain. Nat. Neurosci. 8 , 1248–1254 (2005).

Sasaki, Y. & Watanabe, T. The primary visual cortex fills in color. Proc. Natl Acad. Sci. USA 101 , 18251–18256 (2004).

Kok, P., Failing, M. F. & de Lange, F. P. Prior expectations evoke stimulus templates in the primary visual cortex. J. Cogn. Neurosci. 26 , 1546–1554 (2014).

Bergmann, J., Genc, E., Kohler, A., Singer, W. & Pearson, J. Smaller primary visual cortex is associated with stronger, but less precise mental imagery. Cereb. Cortex 26 , 3838–3850 (2016). This study shows that stronger but less precise imagery is associated with a smaller primary and secondary visual cortex .

Stensaas, S. S., Eddington, D. K. & Dobelle, W. H. The topography and variability of the primary visual cortex in man. J. Neurosurg. 40 , 747–755 (1974).

Song, C., Schwarzkopf, D. S. & Rees, G. Variability in visual cortex size reflects tradeoff between local orientation sensitivity and global orientation modulation. Nat. Commun. 4 , 1–10 (2013).

Google Scholar  

Dorph-Petersen, K.-A., Pierri, J. N., Wu, Q., Sampson, A. R. & Lewis, D. A. Primary visual cortex volume and total neuron number are reduced in schizophrenia. J. Comp. Neurol. 501 , 290–301 (2007).

Sack, A. T., van de Ven, V. G., Etschenberg, S., Schatz, D. & Linden, D. E. J. Enhanced vividness of mental imagery as a trait marker of schizophrenia? Schizophr. Bull. 31 , 97–104 (2005).

Maróthi, R. & Kéri, S. Enhanced mental imagery and intact perceptual organization in schizotypal personality disorder. Psychiatry Res. 259 , 433–438 (2018).

Morina, N., Leibold, E. & Ehring, T. Vividness of general mental imagery is associated with the occurrence of intrusive memories. J. Behav. Ther. Exp. Psychiatry 44 , 221–226 (2013).

Chao, L. L., Lenoci, M. & Neylan, T. C. Effects of post-traumatic stress disorder on occipital lobe function and structure. Neuroreport 23 , 412–419 (2012).

Tavanti, M. et al. Evidence of diffuse damage in frontal and occipital cortex in the brain of patients with post-traumatic stress disorder. Neurol. Sci. 33 , 59–68 (2011).

Kavanagh, D. J., Andrade, J. & May, J. Imaginary relish and exquisite torture: the elaborated intrusion theory of desire. Psychol. Rev. 112 , 446–467 (2005).

Ersche, K. D. et al. Abnormal brain structure implicated in stimulant drug addiction. Science 335 , 601–604 (2012).

Song, C., Schwarzkopf, D. S., Kanai, R. & Rees, G. Reciprocal anatomical relationship between primary sensory and prefrontal cortices in the human brain. J. Neurosci. 31 , 9472–9480 (2011).

Panizzon, M. S. et al. Distinct genetic influences on cortical surface area and cortical thickness. Cereb. Cortex 19 , 2728–2735 (2009).

Winkler, A. M. et al. Cortical thickness or grey matter volume? The importance of selecting the phenotype for imaging genetics studies. Neuroimage 53 , 1135–1146 (2010).

Bakken, T. E. et al. Association of common genetic variants in GPCPD1 with scaling of visual cortical surface area in humans. Proc. Natl Acad. Sci. USA 109 , 3985–3990 (2012).

Pearson, J., Rademaker, R. L. & Tong, F. Evaluating the mind’s eye: the metacognition of visual imagery. Psychol. Sci. 22 , 1535–1542 (2011).

Rademaker, R. L. & Pearson, J. Training visual imagery: improvements of metacognition, but not imagery strength. Front. Psychol. 3 , 224 (2012).

Pearson, J. New directions in mental-imagery research: the binocular-rivalry technique and decoding fMRI patterns. Curr. Dir. Psychol. Sci. 23 , 178–183 (2014).

Keogh, R., Bergmann, J. & Pearson, J. Cortical excitability controls the strength of mental imagery. Preprint at bioRxiv https://www.biorxiv.org/content/10.1101/093690v1 (2016).

Terhune, D. B., Tai, S., Cowey, A., Popescu, T. & Kadosh, R. C. Enhanced cortical excitability in grapheme-color synesthesia and its modulation. Curr. Biol. 21 , 2006–2009 (2011).

Chiou, R., Rich, A. N., Rogers, S. & Pearson, J. Exploring the functional nature of synaesthetic colour: dissociations from colour perception and imagery. Cognition 177 , 107–121 (2018).

Arieli, A., Sterkin, A., Grinvald, A. & Aertsen, A. Dynamics of ongoing activity: explanation of the large variability in evoked cortical responses. Science 273 , 1868–1871 (1996).

Wassell, J., Rogers, S. L., Felmingam, K. L., Bryant, R. A. & Pearson, J. Biological psychology. Biol. Psychol. 107 , 61–68 (2015).

Kraehenmann, R. et al. LSD increases primary process thinking via serotonin 2A receptor activation. Front. Pharmacol. 8 , 418–419 (2017).

Article   CAS   Google Scholar  

Pearson, J., Clifford, C. W. G. & Tong, F. The functional impact of mental imagery on conscious perception. Curr. Biol. 18 , 982–986 (2008). This study shows that the content of visual imagery can bias or prime subsequent binocular rivalry; this paper was the basis for using binocular rivalry as a measurement tool for imagery .

Ishai, A. & Sagi, D. Common mechanisms of visual imagery and perception. Science 268 , 1772–1774 (1995).

Tartaglia, E. M., Bamert, L., Mast, F. W. & Herzog, M. H. Human perceptual learning by mental imagery. Curr. Biol. 19 , 2081–2085 (2009). This study shows that training with a purely imaged visual stimulus transfers to improve performance in perceptual tasks .

Lewis, D. E., O’Reilly, M. J. & Khuu, S. K. Conditioning the mind’s eye associative learning with voluntary mental imagery. Clin. Psychol. Sci. 1 , 390–400 (2013).

Laeng, B. & Sulutvedt, U. The eye pupil adjusts to imaginary light. Psychol. Sci. 25 , 188–197 (2014).

Brascamp, J. W., Knapen, T. H. J., Kanai, R., van Ee, R. & van den Berg, A. V. Flash suppression and flash facilitation in binocular rivalry. J. Vis. 7 , 12 (2007).

Tanaka, Y. & Sagi, D. A perceptual memory for low-contrast visual signals. Proc. Natl Acad. Sci. USA 95 , 12729–12733 (1998).

Chang, S., Lewis, D. E. & Pearson, J. The functional effects of color perception and color imagery. J. Vis. 13 , 4 (2013).

Slotnick, S. D., Thompson, W. L. & Kosslyn, S. M. Visual mental imagery induces retinotopically organized activation of early visual areas. Cereb. Cortex 15 , 1570–1583 (2005).

Thirion, B. et al. Inverse retinotopy: inferring the visual content of images from brain activation patterns. Neuroimage 33 , 1104–1116 (2006).

Horikawa, T. & Kamitani, Y. Generic decoding of seen and imagined objects using hierarchical visual features. Nat. Commun. 8 , 15037 (2017).

Keogh, R. & Pearson, J. Mental imagery and visual working memory. PLOS ONE 6 , e29221 (2011).

Keogh, R. & Pearson, J. The sensory strength of voluntary visual imagery predicts visual working memory capacity. J. Vis. 14 , 7 (2014).

Aydin, C. The differential contributions of visual imagery constructs on autobiographical thinking. Memory 26 , 189–200 (2017).

Schacter, D. L. et al. The future of memory: remembering, imagining, and the brain. Neuron 76 , 677–694 (2012).

Tong, F. Imagery and visual working memory: one and the same? Trends Cogn. Sci. 17 , 489–490 (2013).

Berger, G. H. & Gaunitz, S. C. Self-rated imagery and encoding strategies in visual memory. Br. J. Psychol. 70 , 21–24 (1979).

Harrison, S. A. & Tong, F. Decoding reveals the contents of visual working memory in early visual areas. Nature 458 , 632–635 (2009).

Borst, G., Ganis, G., Thompson, W. L. & Kosslyn, S. M. Representations in mental imagery and working memory: evidence from different types of visual masks. Mem. Cognit. 40 , 204–217 (2011).

Kang, M.-S., Hong, S. W., Blake, R. & Woodman, G. F. Visual working memory contaminates perception. Psychon Bull. Rev. 18 , 860–869 (2011).

Keogh, R. & Pearson, J. The perceptual and phenomenal capacity of mental imagery. Cognition 162 , 124–132 (2017). This study shows a new method to measure the capacity function of visual imagery and shows that it is quite limited .

Luck, S. J. & Vogel, E. K. Visual working memory capacity: from psychophysics and neurobiology to individual differences. Trends Cogn. Sci. 17 , 391–400 (2013).

Pearson, J. & Keogh, R. Redefining visual working memory: a cognitive-strategy, brain-region approach. Curr. Dir. Psychol. Sci. 28 , 266–273 (2019).

Greenberg, D. L. & Knowlton, B. J. The role of visual imagery in autobiographical memory. Mem. Cognit. 42 , 922–934 (2014).

Sheldon, S., Amaral, R. & Levine, B. Individual differences in visual imagery determine how event information is remembered. Memory 25 , 360–369 (2017).

D’Argembeau, A. & Van der Linden, M. Individual differences in the phenomenology of mental time travel: the effect of vivid visual imagery and emotion regulation strategies. Conscious Cogn. 15 , 342–350 (2006).

Vannucci, M., Pelagatti, C., Chiorri, C. & Mazzoni, G. Visual object imagery and autobiographical memory: object Imagers are better at remembering their personal past. Memory 24 , 455–470 (2015).

Galton, F. Statistics of mental imagery. Mind 5 , 301–318 (1880). This paper was the first formal empirical paper investing imagery vividness, including the first report of what is now called aphantasia .

Holmes, E. A. & Mathews, A. Mental imagery in emotion and emotional disorders. Clin. Psychol. Rev. 30 , 349–362 (2010).

Hackmann, A., Bennett-Levy, J. & Holmes, E. A. Oxford Guide to Imagery in Cognitive Therapy (Oxford Univ. Press, 2011).

Blackwell, S. E. et al. Positive imagery-based cognitive bias modification as a web-based treatment tool for depressed adults: a randomized controlled trial. Clin. Psychol. Sci. 3 , 91–111 (2015).

Crane, C., Shah, D., Barnhofer, T. & Holmes, E. A. Suicidal imagery in a previously depressed community sample. Clin. Psychol. Psychother. 19 , 57–69 (2011).

Hales, S. A., Deeprose, C., Goodwin, G. M. & Holmes, E. A. Cognitions in bipolar affective disorder and unipolar depression: imagining suicide. Bipolar Disord. 13 , 651–661 (2011).

Holmes, E. A. et al. Mood stability versus mood instability in bipolar disorder: a possible role for emotional mental imagery. Behav. Res. Ther. 49 , 707–713 (2011).

Tiggemann, M. & Kemps, E. The phenomenology of food cravings: the role of mental imagery. Appetite 45 , 305–313 (2005).

Connor, J. P. et al. Addictive behaviors. Addict. Behav. 39 , 721–724 (2014).

May, J., Andrade, J., Panabokke, N. & Kavanagh, D. Visuospatial tasks suppress craving for cigarettes. Behav. Res. Ther. 48 , 476–485 (2010).

Michael, T., Ehlers, A., Halligan, S. L. & Clark, D. M. Unwanted memories of assault: what intrusion characteristics are associated with PTSD? Behav. Res. Ther. 43 , 613–628 (2005).

Holmes, E. A., James, E. L., Kilford, E. J. & Deeprose, C. Key steps in developing a cognitive vaccine against traumatic flashbacks: visuospatial tetris versus verbal pub quiz. PLOS ONE 5 , e13706 (2010).

Shine, J. M. et al. Imagine that: elevated sensory strength of mental imagery in individuals with Parkinson’s disease and visual hallucinations. Proc. R. Soc. B 282 , 20142047 (2014).

Foa, E. B., Steketee, G., Turner, R. M. & Fischer, S. C. Effects of imaginal exposure to feared disasters in obsessive-compulsive checkers. Behav. Res. Ther. 18 , 449–455 (1980).

Hunt, M. & Fenton, M. Imagery rescripting versus in vivo exposure in the treatment of snake fear. J. Behav. Ther. Exp. Psychiatry 38 , 329–344 (2007).

Holmes, E. A. & Mathews, A. Mental imagery and emotion: a special relationship? Emotion 5 , 489–497 (2005).

Zeman, A. Z. J. et al. Loss of imagery phenomenology with intact visuo-spatial task performance: a case of ‘blind imagination’. Neuropsychologia 48 , 145–155 (2010).

Ungerleider, L. G. & Haxby, J. V. ‘What’ and ‘where’ in the human brain. Curr. Opin. Neurobiol. 4 , 157–165 (1994).

Jacobs, C., Schwarzkopf, D. S. & Silvanto, J. Visual working memory performance in aphantasia. Cortex 105 , 61–73 (2017).

Gray, C. R. & Gummerman, K. The enigmatic eidetic image: a critical examination of methods, data, and theories. Psychol. Bull. 82 , 383–407 (1975).

Stromeyer, C. F. & Psotka, J. The detailed texture of eidetic images. Nature 225 , 346–349 (1970).

Haber, R. N. Twenty years of haunting eidetic imagery: where’s the ghost? Behav. Brain Sci. 2 , 616–617 (1979).

Allport, G. W. Eidetic imagery. Br. J. Psychol. 15 , 99–120 (1924).

Kwok, E. L., Leys, G., Koenig-Robert, R. & Pearson, J. Measuring thought-control failure: sensory mechanisms and individual differences. Psychol. Sci. 57 , 811–821 (2019). This study shows that, even when people think they have successfully suppressed a mental image, it is still actually there and biases subsequent perception (a possible candidate for unconscious imagery) .

Kosslyn, S. M. Image and Mind (Harvard Univ. Press, 1980).

Kosslyn, S. M. Mental images and the brain. Cogn. Neuropsychol. 22 , 333–347 (2005).

Pylyshyn, Z. W. What the mind’s eye tells the mind’s brain: a critique of mental imagery. Psychol. Bull. 80 , 1–24 (1973).

Pylyshyn, Z. Return of the mental image: are there really pictures in the brain? Trends Cogn. Sci. 7 , 113–118 (2003). This review provides an updated summary of the imagery debate .

Chang, S. & Pearson, J. The functional effects of prior motion imagery and motion perception. Cortex 105 , 83–96 (2017).

Stokes, M., Thompson, R., Cusack, R. & Duncan, J. Top-down activation of shape-specific population codes in visual cortex during mental imagery. J. Neurosci. 29 , 1565–1572 (2009).

Amit, E. & Greene, J. D. You see, the ends don’t justify the means: visual imagery and moral judgment. Psychol. Sci. 23 , 861–868 (2012).

Dobson, M. & Markham, R. Imagery ability and source monitoring: implications for eyewitness memory. Br. J. Psychol. 84 , 111–118 (1993).

Gonsalves, B. et al. Neural evidence that vivid imagining can lead to false remembering. Psychol. Sci. 15 , 655–660 (2004).

Bird, C. M., Bisby, J. A. & Burgess, N. The hippocampus and spatial constraints on mental imagery. Front. Hum. Neurosci. 6 , 142 (2012).

Jones, L. & Stuth, G. The uses of mental imagery in athletics: an overview. Appl. Prev. Psychol. 6 , 101–115 (1997).

Dils, A. T. & Boroditsky, L. Visual motion aftereffect from understanding motion language. Proc. Natl Acad. Sci. USA 107 , 16396–16400 (2010).

Christian, B. M., Miles, L. K., Parkinson, C. & Macrae, C. N. Visual perspective and the characteristics of mind wandering. Front. Psychol. 4 , 699 (2013).

Palmiero, M., Cardi, V. & Belardinelli, M. O. The role of vividness of visual mental imagery on different dimensions of creativity. Creat. Res. J. 23 , 372–375 (2011).

Download references

Acknowledgements

The author thanks R. Keogh, R. Koenig-Robert and A. Dawes for helpful feedback and discussion on this paper. This paper, and some of the work discussed in it, was supported by Australian National Health and Medical Research Council grants APP1024800, APP1046198 and APP1085404, a Career Development Fellowship APP1049596 and an Australian Research Council discovery project grant DP140101560.

Author information

Authors and affiliations.

School of Psychology, The University of New South Wales, Sydney, Australia

Joel Pearson

You can also search for this author in PubMed   Google Scholar

Corresponding author

Correspondence to Joel Pearson .

Ethics declarations

Competing interests.

The author declares no competing interests.

Additional information

Peer review information Nature Reviews Neuroscience thanks D. Kavanagh, J. Hohwy and the other, anonymous, reviewer(s) for their contribution to the peer review of this work.

Publisher’s note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

The reverse direction of neural information flow, for example, from the top-down, as opposed to the bottom-up.

Magnetic resonance imaging and functional magnetic resonance imaging decoding methods that are constrained by or based on individual voxel responses to perception, which are then used to decode imagery.

Transformations in a spatial domain.

The conscious sense or feeling of something, different from detection.

A mental disorder characterized by social anxiety, thought disorder, paranoid ideation, derealization and transient psychosis.

Rights and permissions

Reprints and permissions

About this article

Cite this article.

Pearson, J. The human imagination: the cognitive neuroscience of visual mental imagery. Nat Rev Neurosci 20 , 624–634 (2019). https://doi.org/10.1038/s41583-019-0202-9

Download citation

Published : 05 August 2019

Issue Date : October 2019

DOI : https://doi.org/10.1038/s41583-019-0202-9

Share this article

Anyone you share the following link with will be able to read this content:

Sorry, a shareable link is not currently available for this article.

Provided by the Springer Nature SharedIt content-sharing initiative

This article is cited by

Representations of imaginary scenes and their properties in cortical alpha activity.

  • Rico Stecher
  • Daniel Kaiser

Scientific Reports (2024)

Predicting the subjective intensity of imagined experiences from electrophysiological measures of oscillatory brain activity

  • Derek H. Arnold
  • Blake W. Saurels
  • Dietrich S. Schwarzkopf

Visual hallucinations induced by Ganzflicker and Ganzfeld differ in frequency, complexity, and content

  • Oris Shenyan
  • Matteo Lisi
  • Tessa M. Dekker

Neural signatures of imaginary motivational states: desire for music, movement and social play

  • Giada Della Vedova
  • Alice Mado Proverbio

Brain Topography (2024)

Subregions of the fusiform gyrus are differentially involved in the attentional mechanism supporting visual mental imagery in depression

  • Jun-He Zhou
  • Bin-Kun Huang

Brain Imaging and Behavior (2024)

Quick links

  • Explore articles by subject
  • Guide to authors
  • Editorial policies

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

visual perception psychology research paper

Visual Perception Based on Gestalt Theory

  • Conference paper
  • First Online: 26 January 2021
  • Cite this conference paper

visual perception psychology research paper

  • Zhiyuan Ye 19 ,
  • Chenqi Xue 19 &
  • Yun Lin 19  

Part of the book series: Advances in Intelligent Systems and Computing ((AISC,volume 1322))

Included in the following conference series:

  • International Conference on Intelligent Human Systems Integration

3014 Accesses

1 Citations

Gestalt psychology puts forward the laws of similarity, proximity and common destiny. These laws all point out that visual stimuli work together to form a similar pattern organization, which results in the visual elements conforming to the same rules to be regarded as a group by the observer. However, the attributes of visual elements are now more diverse, including the dynamic changes of visual elements. In this paper, based on Bertin’s five visual variables, we will explore the impact of the coordinated changes of these visual variables on human visual perception. The experiment produced the ranking of visual variables on the strength of grouping ability. In practical application, the relative grouping strength of these visual elements has high application value for interface design and data visualization research.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Subscribe and save.

  • Get 10 units per month
  • Download Article/Chapter or Ebook
  • 1 Unit = 1 Article or 1 Chapter
  • Cancel anytime
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
  • Available as EPUB and PDF
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

Similar content being viewed by others

Objective measurement of gestalts: quantifying grouping effect by tilt aftereffect.

visual perception psychology research paper

Interacting with More Than One Chart: What Is It All About?

visual perception psychology research paper

Toward a Better Understanding and Application of the Principles of Visual Communication

Baecker, R., Small, I.: Animation at the interface. In: Laurel, B. (ed.) The Art of Human-Computer Interface Design, pp. 251–267. Addison-Wesley (1990)

Google Scholar  

Dragicevic, P., Bezerianos, A., Javed, W., Elmqvist, N., Fekete, J.-D.: Temporal distortion for animated transitions. In: Proceedings of the ACM Conference on Human Factors in Computing Systems, pp. 2009–2018. ACM, New York (2011). https://doi.org/10.1145/1978942.1979233

Jerison, H.J.: Evolution of the Brain and Intelligence. Academic Press (1973)

Maddox, W.T.: Perceptual and Decisional Separability, chap. Multi-dimensional Models of Perception and Cognition. Lawrence Erlbaum, Hillsdale (1992)

Bertin, J.: Sémiologie graphique. Mouton/Gauthier-Villars, Paris, France (1967)

Sekuler, A.B., Bennett, P.J.: Generalized common fate: grouping by common luminance changes. Psychol. Sci. 12 (6), 437–444 (2001). https://doi.org/10.1111/1467-9280.00382

Article   Google Scholar  

Download references

Acknowledgments

The authors would like to gratefully acknowledge the reviewers’ comments. This work was supported jointly by National Natural Science Foundation of China (No. 71871056, 71471037).

Author information

Authors and affiliations.

School of Mechanical Engineering, Southeast University, Nanjing, China

Zhiyuan Ye, Chenqi Xue & Yun Lin

You can also search for this author in PubMed   Google Scholar

Corresponding author

Correspondence to Chenqi Xue .

Editor information

Editors and affiliations.

Università degli Studi di Palermo, Palermo, Palermo, Italy

Dario Russo

Institute for Advanced Systems Engineering, Florida, FL, USA

Tareq Ahram

University of Central Florida, Orlando, FL, USA

Waldemar Karwowski

Università degli Studi di Chieti-Pescara, Pescara, Italy

Giuseppe Di Bucchianico

Université de Reims Champagne-Ardenne, Reims, France

Redha Taiar

Rights and permissions

Reprints and permissions

Copyright information

© 2021 The Author(s), under exclusive license to Springer Nature Switzerland AG

About this paper

Cite this paper.

Ye, Z., Xue, C., Lin, Y. (2021). Visual Perception Based on Gestalt Theory. In: Russo, D., Ahram, T., Karwowski, W., Di Bucchianico, G., Taiar, R. (eds) Intelligent Human Systems Integration 2021. IHSI 2021. Advances in Intelligent Systems and Computing, vol 1322. Springer, Cham. https://doi.org/10.1007/978-3-030-68017-6_118

Download citation

DOI : https://doi.org/10.1007/978-3-030-68017-6_118

Published : 26 January 2021

Publisher Name : Springer, Cham

Print ISBN : 978-3-030-68016-9

Online ISBN : 978-3-030-68017-6

eBook Packages : Intelligent Technologies and Robotics Intelligent Technologies and Robotics (R0)

Share this paper

Anyone you share the following link with will be able to read this content:

Sorry, a shareable link is not currently available for this article.

Provided by the Springer Nature SharedIt content-sharing initiative

  • Publish with us

Policies and ethics

  • Find a journal
  • Track your research

U.S. flag

An official website of the United States government

The .gov means it’s official. Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

The site is secure. The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

  • Publications
  • Account settings

Preview improvements coming to the PMC website in October 2024. Learn More or Try it out now .

  • Advanced Search
  • Journal List
  • Psychol Sci

Seeing What You Feel: Affect Drives Visual Perception of Structurally Neutral Faces

Erika h. siegel.

1 Department of Health Psychology, University of California, San Francisco

Jolie B. Wormwood

2 Department of Psychology, Northeastern University

Karen S. Quigley

3 Edith Nourse Rogers Memorial Veterans Hospital, Bedford, Massachusetts

Lisa Feldman Barrett

4 Massachusetts General Hospital, Boston, Massachusetts

5 Harvard Medical School, Boston, Massachusetts

Associated Data

Affective realism, the phenomenon whereby affect is integrated into an individual’s experience of the world, is a normal consequence of how the brain processes sensory information from the external world in the context of sensations from the body. In the present investigation, we provided compelling empirical evidence that affective realism involves changes in visual perception (i.e., affect changes how participants see neutral stimuli). In two studies, we used an interocular suppression technique, continuous flash suppression, to present affective images outside of participants’ conscious awareness. We demonstrated that seen neutral faces are perceived as more smiling when paired with unseen affectively positive stimuli. Study 2 also demonstrated that seen neutral faces are perceived as more scowling when paired with unseen affectively negative stimuli. These findings have implications for real-world situations and challenge beliefs that affect is a distinct psychological phenomenon that can be separated from cognition and perception.

Affective realism refers to the idea that affective feelings help to construct your experience of the world ( Anderson, Siegel, White, & Barrett, 2012 ; Barrett & Bar, 2009 ). Feelings do more than influence judgments of what you have seen; they influence the actual content of perception. Affective realism is consistent with neuroscientific evidence that the brain constructs experience by using past experience (i.e., memory) to anticipate sensory inputs and that these signals are corrected by sensory information from the world ( Barrett, 2017 ; Chanes & Barrett, 2016 ; Clark, 2013 ). From this perspective, called predictive coding ( Clark, 2013 ), active inference ( Friston, 2010 ), or belief propagation ( Deneve & Jardri, 2016 ), perceptions derive from the brain’s “predictions” about the causes of sensory events, based on past experience, with incoming sensory input, prediction error , serving to check those predictions. Anatomic, physiologic, and metabolic evidence ( Chanes & Barrett, 2016 ; Kleckner et al., 2017 ) indicates that we do not see the world veridically, with cognition and emotion biasing perception in a top-down fashion. Instead, we see it as we predict it to be (i.e., consistent with our internal model of the body in the world), with sensory inputs confirming or adjusting that internal model.

Neuroscientific and behavioral studies suggest that affective feelings are integral to the brain’s internal model and, thus, perception. The cytoarchitecture of limbic regions puts affective feelings at the top of the brain’s predictive hierarchy, driving predictions throughout the brain as information cascades to primary sensory and motor regions ( Barbas, 2015 ; Barrett & Simmons, 2015 ; Chanes & Barrett, 2016 ). These same regions control allostasis, the process of coordinating resources across physiologic systems to regulate metabolic energy ( Kleckner et al., 2017 ), and the resulting internal sensations, called interoception ( Craig, 2015 ). As a consequence, interoceptive sensations and their low-dimensional representations ( Barrett, 2017 ; Barrett & Bliss-Moreau, 2009 ) are at the core of the brain’s internal model ( Barrett, 2017 ; Chanes & Barrett, 2016 ; Craig, 2015 ) and, therefore, perception. The predictive structure of the brain and the driving role of limbic cortices help explain why affective properties of valence (pleasantness to unpleasantness) and arousal ( Barrett & Russell, 1999 ) are basic features of consciousness, akin to loudness and brightness ( Damasio, 1999 ; James, 1890/2007 ). Affect is not unique to instances of emotion but is present in every conscious moment, including during perceptions of the outside world.

In this article, we show that affective realism changes how people see one another, literally. We used an interocular suppression technique, continuous flash suppression (CFS; Tsuchiya & Koch, 2005 ), in which a neutral face is presented to one eye at full contrast while an affective face is presented to the other eye at low contrast. The neutral face is consciously perceived, whereas the affective face is suppressed from awareness but processed nonetheless. Research using CFS has revealed that affective information presented outside of awareness changes first impressions of neutral faces ( Anderson et al., 2012 ). We demonstrated that affective realism extends beyond broad social judgments to the visual perception of neutral faces: Individuals perceive structurally neutral faces as more smiling or scowling when paired with unconscious, affective information.

Participants

Participants were undergraduate students recruited from Northeastern University with normal or corrected-to-normal vision without glasses. Forty-five participants (30 females, 15 males; age: M = 19.07 years, SD = 1.30) completed the experiment for credit toward the completion of their introductory psychology course. Sample size was determined by conducting a power analysis in G*Power ( Faul, Erdfelder, Lang, & Buchner, 2007 ) using effect sizes from previous research in our laboratory that employed a similar experimental task ( Anderson et al., 2012 , Study 4). This power analysis revealed that for an effect size (η 2 ) of 0.1 to be detected (80% chance) with significance at the 5% level, a sample of at least 40 participants would be required. Two participants were removed prior to analyses because of problems with calibrating the stereoscope during their experimental session, leaving a final sample of 43 participants.

Stimuli and apparatus

Instructions and stimuli were presented using E-Prime (Version 2; Schneider, Eschman, & Zuccolotto, 2012 ). Each participant viewed stimuli through a mirror stereoscope, a visual device that uses mirrors to simultaneously present different images, one to each eye, while leaning his or her chin and forehead on the rests of the device.

Stimuli included photographs of houses used for the contrast adjustment task, described below, and a series of high-contrast Mondrian-type images similar to those used by Tsuchiya and Koch (2005) that were “flashed” during CFS trials (an example trial can be seen in Fig. 1 ).

An external file that holds a picture, illustration, etc.
Object name is 10.1177_0956797617741718-fig1.jpg

Trial structure for face perception task.

Additional stimuli included images of faces with smiling, scowling, and neutral expressions that were pulled from a normed set of facial stimuli developed in our laboratory (IASLab Face Set; http://www.affective-science.org/face-set.shtml ). Images of faces had no visible teeth and were cropped to 150 (width) by 169 (height) pixels at 100 dpi. From these face images, we generated an additional set of morphed facial stimuli for use in response scales during the face perception task. The morphed facial stimuli represented a blend of affective expressions (i.e., smile and neutral expressions and scowl and neutral expressions). Using Abrosoft Fantamorph software (www.fantamorph.com), we morphed images of the same person displaying a neutral expression and smiling and displaying a neutral expression and scowling. Still images were selected at 20% smile (80% neutral), 10% smile (90% neutral), 10% scowl (90% neutral), and 20% scowl (80% neutral). Sample morphed facial stimuli can be seen in Figure 2 . All stimuli were presented in gray scale on a 19-in. monitor.

An external file that holds a picture, illustration, etc.
Object name is 10.1177_0956797617741718-fig2.jpg

Sample response screen. Participants indicated which of the five faces they just saw from a set of five faces that varied from slightly scowling to slightly smiling (1 = 20% scowl, 2 = 10% scowl, 3 = neutral, 4 = 10% smile, 5 = 20% smile).

Contrast adjustment task

We first established eye dominance for each participant using the hole-in-the-card test ( Dolman, 1919 ) because suppression of images under CFS is more easily achieved when images are presented to the nondominant eye. Participants then completed a contrast adjustment task, during which the contrast level of images presented to the nondominant eye under CFS was adjusted to improve suppression on an individual basis. Each trial of the contrast adjustment task lasted 1,200 ms. On a given trial, participants were presented with a fixation point to both eyes for 500 ms. Then, the dominant eye was presented with six Mondrian-type images for 100 ms each; the alternating pattern of Mondrian images helped achieve CFS ( Tsuchiya & Koch, 2005 ). Concurrently, the nondominant eye was presented with an empty frame for 100 ms and then with a low-contrast, low-luminance image of a house (either right-side up or upside down) for 200 ms. An empty frame was then presented in the nondominant eye for the remaining 300 ms. Following this sequence, a backward mask was presented to both eyes for 500 ms. Participants reported the orientation (upside down or right-side up) of the suppressed house image on each trial by clicking one of two keys on the keyboard. Participants also rated their subjective awareness of the suppressed house using the 4-point Perceptual Awareness Scale ( Ramsøy & Overgaard, 2004 ), from 1, no experience , to 4, absolutely clear experience . Images of houses were presented at four discrete contrast levels, created by reducing the contrast and luminance levels of the original photographs to 75%, 50%, 25%, and 12.5%. For the first 20 trials of this task, all house images were presented at 75% contrast with half of the trials containing right-side-up images and half containing upside-down images. If any participant correctly guessed the orientation of the suppressed house on 70% of the trials or reported “no experience” on less than 75% of trials, the contrast level was reduced, and the participant completed another 20 trials of this task at the next lowest contrast level. This procedure was repeated until the participant correctly guessed the orientation on 13 or fewer trials and reported “no experience” on at least 15 trials, or until the 12.5% contrast level was reached. The contrast adjustment task determined the individualized contrast level at which all suppressed images would be presented for the remainder of the experimental tasks for each participant.

Face perception task

See Figure 1 for a visual representation of the trial structure for the face perception task. On each trial of the face perception task, perceivers were presented with a fixation point to both eyes for 500 ms. Following this, the dominant eye was presented with a Mondrian-type image for 100 ms, a face displaying a neutral facial expression (the target face) for 100 ms, another Mondrian-type image for 100 ms, the target face for 100 ms, and then a final Mondrian image for 100 ms. The alternating pattern of the target face and Mondrian images helped to achieve CFS. Concurrently, the nondominant eye was presented with an empty frame for 100 ms and then with a low-contrast, low-luminance face for 200 ms (the suppressed affective face); faces were smiling, were scowling, or displayed a neutral expression. Suppressed affective faces were the opposite gender of the target face. An empty frame was presented in the nondominant eye for the remaining 300 ms. Following this sequence, a backward mask was presented to both eyes for 500 ms.

We used 18 unique neutral target-face identities (9 male, 9 female), and each was matched with a unique identity of the opposite gender (to serve as a paired suppressed face). These identity pairings were consistent across all participants. The facial configurations portrayed by each suppressed identity (i.e., smiling, scowling, neutral) were counterbalanced, however, across participants (i.e., for all participants, Male A, posing a neutral expression, was paired with Female A, but Female A was smiling for some participants and scowling for others, etc.). For each participant, 6 of the suppressed identities (3 male, 3 female) portrayed each of the three expressions (i.e., smiling, scowling, neutral), and the expression of a given suppressed identity did not change throughout the course of the experimental session. For each participant, each neutral target and suppressed affective face pairing was shown 10 times. This resulted in a total of 180 trials (6 neutral target faces × 3 suppressed affective expression conditions × 10 repetitions). The task was divided into two blocks of 90 trials each, and participants were given a 2-minute break to rest their eyes between blocks.

At the conclusion of each trial, following the 500-ms backward mask, participants made two ratings on a standard keyboard. First, they indicated the gender of the face they saw by choosing “male,” “female,” or “don’t know.” They were instructed to choose “don’t know” if they had trouble determining the gender, saw more than one gender or face, or saw a blend of two genders or faces. Because the suppressed face was always the opposite gender of the seen neutral target face, this gender question was used as a trial-by-trial measure of subjective awareness of the suppressed face. All trials in which the suppressed face “broke through” the suppression effect to reach subjective awareness (i.e., where the participant selected the gender of the suppressed face or the “don’t know” option) were excluded from analyses (7.24% of all trials). Thus, we excluded every trial in which participants reported any subjective awareness of another face, not just those in which participants selected the gender of the suppressed face. Participants then completed a perceptual matching task ( Witt & Proffitt, 2005 ), in which they identified the image that best matched their perception of the neutral target face. To do this, they were shown a set of five faces and asked to select which of the five faces they saw on that trial (see Fig. 2 ). All five images were of the seen neutral target face from the trial. However, the faces varied slightly in expression from 20% scowling to neutral to 20% smiling (see details on creation of morphed images in the Stimuli and Apparatus section). For analyses, images were numbered such that lower numbers indicated more scowling and higher numbers indicated more smiling (i.e., 1 = 20% scowl, 2 = 10% scowl, 3 = neutral, 4 = 10% smile, 5 = 20% smile).

Each participant was greeted by a research assistant who confirmed that the participant had normal or corrected-to-normal vision without glasses. The participants then received a brief verbal description of the experiment and provided informed consent. Next, participants provided demographic information, including gender, race, age, and handedness. The researcher assessed the participant’s eye dominance and led the participant into an individual testing room with a computer and a mirror stereoscope. The researcher instructed the participant to sit with his or her head positioned on the chin and forehead rests of the stereoscope. The research assistant calibrated each participant to the stereoscope, adjusting the mirrors and rests as needed so that the stimuli being presented were aligned with the participant’s eyes. Before each of the experimental tasks, the researcher read instructions and watched while the participant completed five practice trials. The researcher left the participant alone in the testing room with the lights off while he or she completed each task. Participants first completed the contrast adjustment task and then the face perception task. At the end of the experimental session, researchers administered a debriefing questionnaire assessing participants’ awareness of the suppressed stimuli and the purpose of the experiment, as well as their comprehension of task instructions. They were then debriefed about the nature of the study and remunerated for their participation.

As predicted, a repeated measures analysis of variance (ANOVA) revealed a significant effect of the suppressed affective stimuli on the visual perception of the seen neutral faces, F (2, 42) = 9.72, p < .001, η 2 = .32, 95% confidence interval (CI) = [0.08, 0.48] (see Fig. 3 ). The data were also examined by estimating a Bayes factor using Bayesian information criteria ( Wagenmakers, Wetzels, Borsboom, & van der Maas, 2011 ), comparing the fit of the data under the null hypothesis and the alternative hypothesis. A two-sided Bayesian repeated measures ANOVA (with a default Cauchy prior width of r = .707) revealed a Bayes factor (BF 10 ) of 62.9, indicating that the observed data are 62.9 times more likely under the alternative hypothesis (that suppressed affective information will influence perception) than under the null hypothesis. A Bayes factor of 62.9 is considered very strong evidence in favor of our hypothesis.

An external file that holds a picture, illustration, etc.
Object name is 10.1177_0956797617741718-fig3.jpg

Violin plots showing mean ratings of seen expressions by suppressed-affective-information condition in Study 1. Individual dots represent each participant’s mean rating for each face type. Rectangular boxes represent the interquartile range of the distribution, with the line in the middle representing the mean. Density of the violin plots represents the density of the data at each value, with wider sections indicating higher density. Error bars represent ±2 SD . Lower ratings for seen expressions correspond to more intensely scowling morphs, whereas higher ratings correspond to more intensely smiling morphs.

Post hoc analyses revealed that seen neutral faces were perceived as having a more smiling expression when paired with a suppressed affectively positive stimulus ( M = 3.18, SD = 0.33, 95% CI = [3.08, 3.28]) than when paired with either a suppressed affectively neutral stimulus ( M = 3.08, SD = 0.28, 95% CI = [3.00, 3.16]), p = .03, or a suppressed affectively negative stimulus ( M = 3.01, SD = 0.30, 95% CI = [2.92, 3.10]), p < .001. Neutral faces were, in turn, perceived as having a more smiling expression when paired with a suppressed affectively neutral stimulus than a suppressed affectively negative stimulus, p = .04. There were no differences in reaction time across the affective conditions, nor were there any differences in the number of breakthrough trials across affective conditions (during which participants reported conscious awareness of smiling, scowling, and neutral faces at similar rates), F s < 1.04.

Study 2 replicated Study 1 but included an additional objective detection task (detecting a stimulus behaviorally, regardless of subjective awareness; Cheesman & Merikle, 1984 ). When coupled with the trial-by-trial measure, this provided a more robust, converging assessment of awareness.

Seventy-one participants (41 females, 29 males, 1 nonresponse; age: M = 23.56 years, SD = 8.09) were recruited from Northeastern University and the surrounding Boston community who had normal or corrected-to-normal vision without glasses. Sample size was determined on the basis of a power analysis calculated for Study 1, adjusted to accommodate expected data exclusions due to better-than-chance performance on the objective awareness task ( Anderson et al., 2012 ). Participants either received credit toward the completion of their introductory psychology course requirements or received $5 per half hour of participation. Prior to analyses, we removed 4 participants who reported completing other experiments in the laboratory that used CFS. One additional participant was removed from analyses because of problems with calibrating the stereoscope during the experimental session, leaving a final sample of 66 participants.

Materials, tasks, and procedure

Materials and tasks in Study 2 were identical to those of Study 1, except that an additional task was completed at the end of the experiment as a second measure of awareness of the suppressed affective faces (to complement the trial-by-trial measure of awareness used in Study 1). With the exception of this additional task, the procedure was identical across Studies 1 and 2.

Objective awareness task

Trials in the objective awareness task were nearly identical to the experimental trials in the face perception task except that (a) suppressed affective faces were presented upside down on half of the trials, and (b) a scrambled image of a face (which was no longer identifiable as a face) was presented to the dominant eye (instead of a neutral target face). Participants completed 72 trials of this task; we presented each of the 18 unique suppressed affective faces from the face perception task four times, twice right-side up and twice upside down (rotated 180°). These suppressed affective faces were presented at the same contrast level as used in the face perception task for each participant. At the conclusion of each trial, participants were asked to guess the orientation of the face (upside down or right-side up) and then to rate the quality of their visual experience on the same 4-point Perceptual Awareness Scale ( Ramsøy & Overgaard, 2004 ) used during the contrast adjustment task. If images presented to the nondominant eye were not successfully suppressed throughout the experiment, participants should have some conscious awareness of the faces and should report the correct orientation of the suppressed affective faces at better-than-chance level during this objective awareness task.

Eighteen of the 66 participants were able to correctly guess the orientation of the suppressed face on 62.5% or more of the trials (better than chance, p < .05, two-tailed). These participants were excluded from all further analyses ( n = 48). Moreover, in Study 2, we again excluded individual trials of the face perception task on which breakthrough may have occurred: 10.78% of all face perception trials were removed prior to analyses because participants failed to accurately report the gender of the seen neutral target face.

Replicating Study 1, a repeated measures ANOVA revealed a significant effect of suppressed affective stimuli on the visual perception of the seen neutral faces, F (2, 47) = 3.62, p = .03, η 2 = .07, 95% CI = [0.00, 0.18] (see Fig. 4 ). A two-sided Bayesian repeated measures ANOVA revealed a BF 10 of 1.4, indicating that the observed data are 1.4 times more likely under the alternative hypothesis (that suppressed affective information will influence perception) than under the null hypothesis. Whereas a Bayes factor of 1.4 is considered anecdotal evidence in favor of our hypothesis, these findings directly replicate those of Experiment 1 (which had a Bayes factor considered “very strong” evidence in favor of our hypothesis) and do so even with the implementation of highly conservative inclusion criteria based on the robust, converging assessments of awareness used in Experiment 2.

An external file that holds a picture, illustration, etc.
Object name is 10.1177_0956797617741718-fig4.jpg

Violin plots showing mean ratings of seen expressions by suppressed-affective-information condition in Study 2. Individual dots represent each participant’s mean rating for each face type. Rectangular boxes represent the interquartile range of the distribution, with the line in the middle representing the mean. Density of the violin plots represents the density of the data at each value, with wider sections indicating higher density. Error bars represent ±2 SD . Lower ratings for seen expressions correspond to more intensely scowling morphs, whereas higher ratings correspond to more intensely smiling morphs.

Post hoc analyses revealed that seen neutral faces were perceived as having a more smiling expression when paired with a suppressed affectively positive stimulus ( M = 3.10, SD = 0.38, 95% CI = [2.99, 3.21]) than when paired with either a suppressed affectively neutral stimulus ( M = 3.02, SD = 0.37, 95% CI = [2.92, 3.13]), p = .04, or a suppressed affectively negative stimulus ( M = 3.02, SD = 0.36, 95% CI = [2.92, 3.12]), p = .04. In this study, perceptions of seen neutral faces did not differ significantly when paired with a suppressed affectively neutral stimulus or a suppressed affectively negative stimulus, p = .97. Thus, the effect for negative stimuli was smaller in Study 2 than in Study 1, but in both studies, neutral faces were perceived as more smiling in trials with suppressed positive stimuli than in trials with suppressed negative stimuli. There were no differences in reaction time across the affective conditions, nor were there any differences in the number of breakthrough trials by suppressed affective condition (i.e., participants reported conscious awareness of smiling, scowling, and neutral faces at similar rates), F s < 1.69.

General Discussion

Affective realism provides a novel framework for understanding affective misattribution effects ( Clore, Gasper, & Garvin, 2001 ) and represents a critical extension of work on the role of affect in perception, which has largely focused on lower-level perceptual effects, such as sensitivity for contrast gradients and global versus local feature processing (for a review, see Zadra & Clore, 2011 ). To our knowledge, we are the first to demonstrate the role of affect in the perception of complex percepts that carry social meaning. The two studies reported here demonstrate that visual percepts are infused with affect. Previous research provided evidence that individuals experience neutral faces differently (i.e., as more likeable or trustworthy) depending on the affective feelings accompanying those faces ( Anderson et al., 2012 ). Our data add to this literature, suggesting that individuals perceive faces differently depending on their affective feelings.

There is debate about whether perceptual matching tasks (such as ours) measure perception or memory ( Philbeck & Witt, 2015 ), but accumulating empirical evidence indicates that the boundary between perception and memory is more phenomenological than physically real (see Fan, Hutchinson, & Turk-Browne, 2016 ). Visual perception and visual memory are associated with the same neural substrates and rely on shared processes ( Slotnick & Schacter, 2004 ; Ungerleider, 1995 ). Predictive coding approaches provide further support by suggesting that perceptions are memories, constrained and corrected by sensory inputs from the outside world ( Barrett, 2017 ; Clark, 2013 ; Summerfield et al., 2006 ). What a person consciously sees in the moment is a mental representation of the real world, not a direct reflection of it. In our studies, incidental affect was perceived as a property of seen faces in the same way that red is perceived as a property of a rose.

The present studies highlight several important avenues for future research. First, assessing participants’ confidence in their perceptual experience might offer insight into whether affective realism involves modulations in perceptual precision, particularly as affect has been shown to influence confidence ratings in other perceptual modalities ( Allen et al., 2016 ). Future research should explore affective realism across different levels of awareness while exploring the extent of neural processing (e.g., Jiang & He, 2006 ). Furthermore, using affective stimuli other than faces (e.g., snakes) may also speak to the robustness of affective realism.

That we perceive others differently depending on how we feel may have important real-world implications. For instance, the affective-realism hypothesis may help to explain why police officers perceive targets as more or less threatening depending on the interoceptive information they receive ( Azevedo, Garfinkel, Critchley, & Tsakiris, 2017 ). Research on affective realism stands to fundamentally alter our understanding of how perception influences decision making in real-world scenarios where errors can have costly, potentially deadly, consequences.

Supplementary Material

Action Editor: Alice O’Toole served as action editor for this article.

Author Contributions: E. H. Siegel and J. B. Wormwood contributed equally to this study. All authors contributed to the study concept and design. Data were collected and analyzed by E. H. Siegel and J. B. Wormwood under the supervision of K. S. Quigley and L. F. Barrett. E. H. Siegel and J. B. Wormwood drafted the manuscript, and K. S. Quigley and L. F. Barrett provided critical revisions. All authors approved the final version of the manuscript for submission.

Declaration of Conflicting Interests: The author(s) declared that there were no conflicts of interest with respect to the authorship or the publication of this article.

Funding: This research was supported by the U.S. Army Research Institute for the Behavioral and Social Sciences (Grant W5J9CQ-12-C-0049 to L. F. Barrett and Grant W911N-16-1-0191 to K. S. Quigley and J. B. Wormwood) and a National Institute of Mental Health T32 grant (MH019391) to E. H. Siegel. The views, opinions, and findings contained in this article are those of the authors and shall not be construed as an official Department of the Army position, policy, or decision, unless so designated by other documents.

An external file that holds a picture, illustration, etc.
Object name is 10.1177_0956797617741718-img1.jpg

All data have been made publicly available via the Open Science Framework and can be accessed at osf.io/ht3gk. The complete Open Practices Disclosure for this article can be found at http://journals.sagepub.com/doi/suppl/10.1177/0956797617741718 . This article has received the badge for Open Data. More information about the Open Practices badges can be found at http://www.psychologicalscience.org/publications/badges .

  • Allen M., Frank D., Schwarzkopf D. S., Fardo F., Winston J. S., Hauser T. U., Rees G. (2016). Unexpected arousal modulates the influence of sensory noise on confidence . eLife , 5 , Article e18103. doi: 10.7554/eLife.18103 [ PMC free article ] [ PubMed ] [ CrossRef ] [ Google Scholar ]
  • Anderson E., Siegel E. H., White D., Barrett L. F. (2012). Out of sight but not out of mind: Unseen affective faces influence evaluations and social impressions . Emotion , 12 , 1210–1221. [ PMC free article ] [ PubMed ] [ Google Scholar ]
  • Azevedo R. T., Garfinkel S. N., Critchley H. D., Tsakiris M. (2017). Cardiac afferent activity modulates the expression of racial stereotypes . Nature Communications , 8 , Article e13854. doi: 10.1038/ncomms13854 [ PMC free article ] [ PubMed ] [ CrossRef ] [ Google Scholar ]
  • Barbas H. (2015). General cortical and special prefrontal connections: Principles from structure to function . Annual Review of Neuroscience , 38 , 269–289. [ PubMed ] [ Google Scholar ]
  • Barrett L. F. (2017). How emotions are made: The secret life of the brain . New York, NY: Houghton Mifflin Harcourt. [ Google Scholar ]
  • Barrett L. F., Bar M. (2009). See it with feeling: Affective predictions during object perception . Philosophical Transactions of the Royal Society B: Biological Sciences , 364 , 1325–1334. [ PMC free article ] [ PubMed ] [ Google Scholar ]
  • Barrett L. F., Bliss-Moreau E. (2009). Affect as a psychological primitive . In Zanna M. P. (Ed.), Advances in experimental social psychology (Vol. 41 , pp. 167–218). San Diego, CA: Academic Press. [ PMC free article ] [ PubMed ] [ Google Scholar ]
  • Barrett L. F., Russell J. A. (1999). The structure of current affect controversies and emerging consensus . Current Directions in Psychological Science , 8 , 10–14. [ Google Scholar ]
  • Barrett L. F., Simmons W. K. (2015). Interoceptive predictions in the brain . Nature Reviews Neuroscience , 16 , 419–429. [ PMC free article ] [ PubMed ] [ Google Scholar ]
  • Chanes L., Barrett L. F. (2016). Redefining the role of limbic areas in cortical processing . Trends in Cognitive Sciences , 20 , 96–106. [ PMC free article ] [ PubMed ] [ Google Scholar ]
  • Cheesman J., Merikle P. M. (1984). Priming with and without awareness . Perception & Psychophysics , 36 , 387–395. [ PubMed ] [ Google Scholar ]
  • Clark A. (2013). Whatever next? Predictive brains, situated agents, and the future of cognitive science . Behavioral & Brain Sciences , 36 , 181–204. [ PubMed ] [ Google Scholar ]
  • Clore G. L., Gasper K., Garvin E. (2001). Affect as information . In Forgas J. P. (Ed.), Handbook of affect and social cognition (pp. 121–144). Mahwah, NJ: Erlbaum. [ Google Scholar ]
  • Craig A. D. (2015). How do you feel? An interoceptive moment with your neurobiological self . Princeton, NJ: Princeton University Press. [ Google Scholar ]
  • Damasio A. R. (1999). The feeling of what happens: Body and emotion in the making of consciousness . New York, NY: Houghton Mifflin Harcourt. [ Google Scholar ]
  • Deneve S., Jardri R. (2016). Circular inference: Mistaken belief, misplaced trust . Current Opinion in Behavioral Sciences , 11 , 40–48. [ Google Scholar ]
  • Dolman P. (1919). Tests for determining the sighting eye . American Journal of Ophthalmology , 2 , 867. [ Google Scholar ]
  • Fan J. E., Hutchinson J. B., Turk-Browne N. B. (2016). When past is present: Substitutions of long-term memory for sensory evidence in perceptual judgments . Journal of Vision , 16 ( 8 ), Article 1. doi: 10.1167/16.8.1 [ PMC free article ] [ PubMed ] [ CrossRef ] [ Google Scholar ]
  • Faul F., Erdfelder E., Lang A.-G., Buchner A. (2007). G*Power 3: A flexible statistical power analysis program for the social, behavioral, and biomedical sciences . Behavior Research Methods , 39 , 175–191. doi: 10.3758/bf03193146 [ PubMed ] [ CrossRef ] [ Google Scholar ]
  • Friston K. (2010). The free-energy principle: A unified brain theory? Nature Reviews Neuroscience , 11 , 127–138. [ PubMed ] [ Google Scholar ]
  • James W. (2007). The principles of psychology ( Vol. 1 ). New York, NY: Dover. (Original work published 1890) [ Google Scholar ]
  • Jiang Y., He S. (2006). Cortical responses to invisible faces: Dissociating subsystems for facial-information processing . Current Biology , 16 , 2023–2029. [ PubMed ] [ Google Scholar ]
  • Kleckner I. R., Zhang J., Touroutoglou A., Chanes L., Xia C., Simmons W. K., . . . Barrett L. F. (2017). Evidence for a large-scale brain system supporting allostasis and interoception in humans . Nature Human Behaviour, 1 , Article 0069. doi: 10.1038/s41562-017-0069 [ PMC free article ] [ PubMed ] [ CrossRef ] [ Google Scholar ]
  • Philbeck J. W., Witt J. K. (2015). Action-specific influences on perception and postperceptual processes: Present controversies and future directions . Psychological Bulletin , 141 , 1120–1144. [ PMC free article ] [ PubMed ] [ Google Scholar ]
  • Ramsøy T. Z., Overgaard M. (2004). Introspection and subliminal perception . Phenomenology and the Cognitive Sciences , 3 , 1–23. [ Google Scholar ]
  • Schneider W., Eschman A., Zuccolotto A. (2012). E-Prime 2.0 reference guide manual . Pittsburgh, PA: Psychology Software Tools. [ Google Scholar ]
  • Slotnick S. D., Schacter D. L. (2004). A sensory signature that distinguishes true from false memories . Nature Neuroscience , 7 , 664–672. [ PubMed ] [ Google Scholar ]
  • Summerfield C., Egner T., Greene M., Koechlin E., Mangels J., Hirsch J. (2006). Predictive codes for forthcoming perception in the frontal cortex . Science , 314 , 1311–1314. doi: 10.1126/science.1132028 [ PubMed ] [ CrossRef ] [ Google Scholar ]
  • Tsuchiya N., Koch C. (2005). Continuous flash suppression reduces negative afterimages . Nature Neuroscience , 8 , 1096–1101. [ PubMed ] [ Google Scholar ]
  • Ungerleider L. G. (1995). Functions of brain imaging studies of cortical mechanisms for memory . Science , 270 , 769–774. [ PubMed ] [ Google Scholar ]
  • Wagenmakers E. J., Wetzels R., Borsboom D., van der Maas H. L. (2011). Why psychologists must change the way they analyze their data: The case of psi: Comment on Bem (2011) . Journal of Personality and Social Psychology , 100 , 426–432. doi: 10.1037/a0022780 [ PubMed ] [ CrossRef ] [ Google Scholar ]
  • Witt J. K., Proffitt D. R. (2005). See the ball, hit the ball: Apparent ball size is correlated with batting average . Psychological Science , 16 , 937–938. [ PubMed ] [ Google Scholar ]
  • Zadra J. R., Clore G. L. (2011). Emotion and perception: The role of affective information . Wiley Interdisciplinary Reviews: Cognitive Science , 2 , 676–685. [ PMC free article ] [ PubMed ] [ Google Scholar ]

Visual Perception Theory In Psychology

Saul Mcleod, PhD

Editor-in-Chief for Simply Psychology

BSc (Hons) Psychology, MRes, PhD, University of Manchester

Saul Mcleod, PhD., is a qualified psychology teacher with over 18 years of experience in further and higher education. He has been published in peer-reviewed journals, including the Journal of Clinical Psychology.

Learn about our Editorial Process

Olivia Guy-Evans, MSc

Associate Editor for Simply Psychology

BSc (Hons) Psychology, MSc Psychology of Education

Olivia Guy-Evans is a writer and associate editor for Simply Psychology. She has previously worked in healthcare and educational sectors.

On This Page:

perception vs sensation

What is Visual Perception?

To receive information from the environment, we are equipped with sense organs, e.g., the eye, ear, and nose.  Each sense organ is part of a sensory system that receives sensory inputs and transmits sensory information to the brain.

A particular problem for psychologists is explaining how the physical energy received by sense organs forms the basis of perceptual experience. Sensory inputs are somehow converted into perceptions of desks and computers, flowers and buildings, cars and planes, into sights, sounds, smells, tastes, and touch experiences.

A major theoretical issue on which psychologists are divided is the extent to which perception relies directly on the information present in the environment.  Some argue that perceptual processes are not direct but depend on the perceiver’s expectations and previous knowledge as well as the information available in the stimulus itself.

perception theories

This controversy is discussed with respect to Gibson (1966), who has proposed a direct theory of perception which is a “bottom-up” theory, and Gregory (1970), who has proposed a constructivist (indirect) theory of perception which is a “top-down” theory.

Psychologists distinguish between two types of processes in perception: bottom-up processing and top-down processing .

Bottom-up processing is also known as data-driven processing because perception begins with the stimulus itself. Processing is carried out in one direction from the retina to the visual cortex, with each successive stage in the visual pathway carrying out an ever more complex analysis of the input.

Top-down processing refers to the use of contextual information in pattern recognition. For example, understanding difficult handwriting is easier when reading complete sentences than reading single and isolated words. This is because the meaning of the surrounding words provides a context to aid understanding.

Gregory (1970) and Top-Down Processing Theory

what is top-down processing in visual perception

Psychologist Richard Gregory (1970) argued that perception is a constructive process that relies on top-down processing.

Stimulus information from our environment is frequently ambiguous, so to interpret it, we require higher cognitive information either from past experiences or stored knowledge in order to make inferences about what we perceive. Helmholtz called it the ‘likelihood principle’.

For Gregory, perception is a hypothesis which is based on prior knowledge. In this way, we are actively constructing our perception of reality based on our environment and stored information.

  • A lot of information reaches the eye, but much is lost by the time it reaches the brain (Gregory estimates about 90% is lost).
  • Therefore, the brain has to guess what a person sees based on past experiences. We actively construct our perception of reality.
  • Richard Gregory proposed that perception involves a lot of hypothesis testing to make sense of the information presented to the sense organs.
  • Our perceptions of the world are hypotheses based on past experiences and stored information.
  • Sensory receptors receive information from the environment, which is then combined with previously stored information about the world which we have built up as a result of experience.
  • The formation of incorrect hypotheses will lead to errors of perception (e.g., visual illusions like the Necker cube).

Supporting Evidence

There seems to be an overwhelming need to reconstruct the face, similar to Helmholtz’s description of “unconscious inference.” An assumption based on past experience.

Perceptions can be ambiguous

necker cube

The Necker cube is a good example of this. When you stare at the crosses on the cube, the orientation can suddenly change or “flip.”

It becomes unstable, and a single physical pattern can produce two perceptions.

Gregory argued that this object appears to flip between orientations because the brain develops two equally plausible hypotheses and is unable to decide between them.

When the perception changes though there is no change in the sensory input, the change of appearance cannot be due to bottom-up processing. It must be set downwards by the prevailing perceptual hypothesis of what is near and what is far.

Perception allows behavior to be generally appropriate to non-sensed object characteristics.

Critical Evaluation of Gregory’s Theory

1. the nature of perceptual hypotheses.

If perceptions make use of hypothesis testing, the question can be asked, “what kind of hypotheses are they?” Scientists modify a hypothesis according to the support they find for it, so are we, as perceivers, also able to modify our hypotheses? In some cases, it would seem the answer is yes.  For example, look at the figure below:

perception

This probably looks like a random arrangement of black shapes. In fact, there is a hidden face in there; can you see it? The face is looking straight ahead and is in the top half of the picture in the center.  Now can you see it?  The figure is strongly lit from the side and has long hair and a beard.

Once the face is discovered, very rapid perceptual learning takes place and the ambiguous picture now obviously contains a face each time we look at it. We have learned to perceive the stimulus in a different way.

Although in some cases, as in the ambiguous face picture, there is a direct relationship between modifying hypotheses and perception, in other cases, this is not so evident.  For example, illusions persist even when we have full knowledge of them (e.g., the inverted face, Gregory 1974).

One would expect that the knowledge we have learned (from, say, touching the face and confirming that it is not “normal”) would modify our hypotheses in an adaptive manner. The current hypothesis testing theories cannot explain this lack of a relationship between learning and perception.

2. Perceptual Development

A perplexing question for the constructivists who propose perception is essentially top-down in nature is “how can the neonate ever perceive?”  If we all have to construct our own worlds based on past experiences, why are our perceptions so similar, even across cultures?  Relying on individual constructs for making sense of the world makes perception a very individual and chancy process.

The constructivist approach stresses the role of knowledge in perception and therefore is against the nativist approach to perceptual development.

However, a substantial body of evidence has been accrued favoring the nativist approach. For example, Newborn infants show shape constancy (Slater & Morison, 1985); they prefer their mother’s voice to other voices (De Casper & Fifer, 1980); and it has been established that they prefer normal features to scrambled features as early as 5 minutes after birth.

3. Sensory Evidence

Perhaps the major criticism of the constructivists is that they have underestimated the richness of sensory evidence available to perceivers in the real world (as opposed to the laboratory, where much of the constructivists” evidence has come from).

Constructivists like Gregory frequently use the example of size constancy to support their explanations. That is, we correctly perceive the size of an object even though the retinal image of an object shrinks as the object recedes. They propose that sensory evidence from other sources must be available for us to be able to do this.

However, in the real world, retinal images are rarely seen in isolation (as is possible in the laboratory). There is a rich array of sensory information, including other objects, background, the distant horizon, and movement. This rich source of sensory information is important to the second approach to explaining perception that we will examine, namely the direct approach to perception as proposed by Gibson.

Gibson argues strongly against the idea that perception involves top-down processing and criticizes Gregory’s discussion of visual illusions on the grounds that they are artificial examples and not images found in our normal visual environments.

This is crucial because Gregory accepts that misperceptions are the exception rather than the norm. Illusions may be interesting phenomena, but they might not be that information about the debate.

Gibson (1966) and Bottom-Up Processing

Gibson’s bottom-up theory suggests that perception involves innate mechanisms forged by evolution and that no learning is required. This suggests that perception is necessary for survival – without perception, we would live in a very dangerous environment.

Our ancestors would have needed perception to escape from harmful predators, suggesting perception is evolutionary.

James Gibson (1966) argues that perception is direct and not subject to hypothesis testing, as Gregory proposed. There is enough information in our environment to make sense of the world in a direct way.

His theory is sometimes known as the ‘Ecological Theory’ because of the claim that perception can be explained solely in terms of the environment.

For Gibson: the sensation is perception: what you see is what you get.  There is no need for processing (interpretation) as the information we receive about size, shape, distance, etc., is sufficiently detailed for us to interact directly with the environment.

Gibson (1972) argued that perception is a bottom-up process, which means that sensory information is analyzed in one direction: from simple analysis of raw sensory data to the ever-increasing complexity of analysis through the visual system.

what is bottom-up processing in visual perception

Features of Gibson’s Theory

The optic array.

Perception involves ‘picking up’ the rich information provided by the optic array in a direct way with little/no processing involved.

Because of movement and different intensities of light shining in different directions, it is an ever-changing source of sensory information. Therefore, if you move, the structure of the optic array changes.

According to Gibson, we have the mechanisms to interpret this unstable sensory input, meaning we experience a stable and meaningful view of the world.

Changes in the flow of the optic array contain important information about what type of movement is taking place. The flow of the optic array will either move from or towards a particular point.

If the flow appears to be coming from the point, it means you are moving towards it. If the optic array is moving towards the point, you are moving away from it.

Invariant Features

the optic array contains invariant information that remains constant as the observer moves. Invariants are aspects of the environment that don’t change. They supply us with crucial information.

Two good examples of invariants are texture and linear perspective.

visual perception psychology research paper

Another invariant is the horizon-ratio relation. The ratio above and below the horizon is constant for objects of the same size standing on the same ground.

OPTICAL ARRAY : The patterns of light that reach the eye from the environment.

RELATIVE BRIGHTNESS : Objects with brighter, clearer images are perceived as closer

TEXTURE GRADIENT : The grain of texture gets smaller as the object recedes. Gives the impression of surfaces receding into the distance.

RELATIVE SIZE : When an object moves further away from the eye, the image gets smaller. Objects with smaller images are seen as more distant.

SUPERIMPOSITION : If the image of one object blocks the image of another, the first object is seen as closer.

HEIGHT IN THE VISUAL FIELD : Objects further away are generally higher in the visual field

Evaluation of Gibson’s (1966) Direct Theory of Perception

Gibson’s theory is a highly ecologically valid theory as it puts perception back into the real world.

A large number of applications can be applied in terms of his theory, e.g., training pilots, runway markings, and road markings.

It’s an excellent explanation for perception when viewing conditions are clear. Gibson’s theory also highlights the richness of information in an optic array and provides an account of perception in animals, babies, and humans.

His theory is reductionist as it seeks to explain perception solely in terms of the environment. There is strong evidence to show that the brain and long-term memory can influence perception. In this case, it could be said that Gregory’s theory is far more plausible.

Gibson’s theory also only supports one side of the nature-nurture debate, that being the nature side. Again, Gregory’s theory is far more plausible as it suggests that what we see with our eyes is not enough, and we use knowledge already stored in our brains, supporting both sides of the debate.

Visual Illusions

Gibson’s emphasis on DIRECT perception provides an explanation for the (generally) fast and accurate perception of the environment. However, his theory cannot explain why perceptions are sometimes inaccurate, e.g., in illusions.

He claimed the illusions used in experimental work constituted extremely artificial perceptual situations unlikely to be encountered in the real world, however, this dismissal cannot realistically be applied to all illusions.

For example, Gibson’s theory cannot account for perceptual errors like the general tendency for people to overestimate vertical extents relative to horizontal ones.

Neither can Gibson’s theory explain naturally occurring illusions. For example, if you stare for some time at a waterfall and then transfer your gaze to a stationary object, the object appears to move in the opposite direction.

Bottom-up or Top-down Processing?

Neither direct nor constructivist theories of perception seem capable of explaining all perceptions all of the time.

Gibson’s theory appears to be based on perceivers operating under ideal viewing conditions, where stimulus information is plentiful and is available for a suitable length of time. Constructivist theories, like Gregory”s, have typically involved viewing under less-than-ideal conditions.

Research by Tulving et al. manipulated both the clarity of the stimulus input and the impact of the perceptual context in a word identification task. As the clarity of the stimulus (through exposure duration) and the amount of context increased, so did the likelihood of correct identification.

However, as the exposure duration increased, so the impact of context was reduced, suggesting that if stimulus information is high, then the need to use other sources of information is reduced.

One theory that explains how top-down and bottom-up processes may be seen as interacting with each other to produce the best interpretation of the stimulus was proposed by Neisser (1976) – known as the “Perceptual Cycle.”

DeCasper, A. J., & Fifer, W. P. (1980). Of human bonding: Newborns prefer their mothers” voices . Science , 208(4448), 1174-1176.

Gibson, J. J. (1966). The Senses Considered as Perceptual Systems. Boston: Houghton Mifflin.

Gibson, J. J. (1972). A Theory of Direct Visual Perception. In J. Royce, W. Rozenboom (Eds.). The Psychology of Knowing . New York: Gordon & Breach.

Gregory, R. (1970). The Intelligent Eye . London: Weidenfeld and Nicolson.

Gregory, R. (1974). Concepts and Mechanisms of Perception . London: Duckworth.

Necker, L. (1832). LXI. Observations on some remarkable optical phenomena seen in Switzerland; and on an optical phenomenon which occurs on viewing a figure of a crystal or geometrical solid . The London and Edinburgh Philosophical Magazine and Journal of Science, 1 (5), 329-337.

Slater, A., Morison, V., Somers, M., Mattock, A., Brown, E., & Taylor, D. (1990). Newborn and older infants” perception of partly occluded objects. Infant behavior and Development , 13(1), 33-49.

Further Information

Trichromatic Theory of Color Vision

Held and Hein (1963) Movement-Produced Stimulation in the Development of Visually Guided Behavior

What do visual illusions teach us?

Print Friendly, PDF & Email

Related Articles

Automatic Processing in Psychology: Definition & Examples

Cognitive Psychology

Automatic Processing in Psychology: Definition & Examples

Controlled Processing in Psychology: Definition & Examples

Controlled Processing in Psychology: Definition & Examples

How Ego Depletion Can Drain Your Willpower

How Ego Depletion Can Drain Your Willpower

What is the Default Mode Network?

What is the Default Mode Network?

Theories of Selective Attention in Psychology

Availability Heuristic and Decision Making

Availability Heuristic and Decision Making

  • A-Z Publications

Annual Review of Psychology

Volume 74, 2023, review article, open access, the development of color perception and cognition.

  • John Maule 1 , Alice E. Skelton 1 , and Anna Franklin 1
  • View Affiliations Hide Affiliations Affiliations: The Sussex Colour Group & Baby Lab, School of Psychology, University of Sussex, Falmer, United Kingdom; email: [email protected]
  • Vol. 74:87-111 (Volume publication date January 2023) https://doi.org/10.1146/annurev-psych-032720-040512
  • First published as a Review in Advance on August 16, 2022
  • Copyright © 2023 by the author(s). This work is licensed under a Creative Commons Attribution 4.0 International License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. See credit lines of images or other third-party material in this article for license information

Color is a pervasive feature of our psychological experience, having a role in many aspects of human mind and behavior such as basic vision, scene perception, object recognition, aesthetics, and communication. Understanding how humans encode, perceive, talk about, and use color has been a major interdisciplinary effort. Here, we present the current state of knowledge on how color perception and cognition develop. We cover the development of various aspects of the psychological experience of color, ranging from low-level color vision to perceptual mechanisms such as color constancy to phenomena such as color naming and color preference. We also identify neurodiversity in the development of color perception and cognition and implications for clinical and educational contexts. We discuss the theoretical implications of the research for understanding mature color perception and cognition, for identifying the principles of perceptual and cognitive development, and for fostering a broader debate in the psychological sciences.

Article metrics loading...

Full text loading...

Literature Cited

  • Achenbach TM , Edelbrock CS. 1983 . Manual for the Child: Behavior Checklist and Child Behavior Profile Burlington: Univ. Vt. [Google Scholar]
  • Albany-Ward K. 2005 . What do you really know about colour blindness?. Br. J. Sch. Nurs. 10 : 4 123– 24 [Google Scholar]
  • Barbur J , Rodriguez-Carmona M. 2015 . Color vision changes in normal aging. Handbook of Color Psychology A Elliot, M Fairchild, A Franklin 180– 96 Cambridge, UK: Cambridge Univ. Press [Google Scholar]
  • Barry J , Mollan S , Burdon M , Jenkins M , Denniston A. 2017 . Development and validation of a questionnaire assessing the quality of life impact of Colour Blindness (CBQoL). BMC Ophthalmol 17 : 1 179 [Google Scholar]
  • Birch J. 2012 . Worldwide prevalence of red-green color deficiency. J. Opt. Soc. Am. A 29 : 3 313– 20 [Google Scholar]
  • Bonnardel V , Pitchford NJ 2006 . Colour categorization in preschoolers. Progress in Colour Studies , Vol. 2 N Pitchford, CP Biggam 121– 38 Amsterdam: John Benjamins [Google Scholar]
  • Bornstein MH. 1975 . Qualities of color vision in infancy. J. Exp. Child. Psychol. 19 : 3 401– 19 [Google Scholar]
  • Bornstein MH , Kessen W , Weiskopf S. 1976 . The categories of hue in infancy. Science 191 : 4223 201– 2 [Google Scholar]
  • Bosten JM , Beer RD , MacLeod DIA. 2015 . What is white?. J. Vis. 15 : 16 5 [Google Scholar]
  • Bosworth RG , Dobkins KR. 2009 . Chromatic and luminance contrast sensitivity in fullterm and preterm infants. J. Vis . 9 : 13 15.1– 16 [Google Scholar]
  • Bosworth RG , Dobkins KR. 2013 . Effects of prematurity on the development of contrast sensitivity: testing the visual experience hypothesis. Vis. Res. 82 : 31– 41 [Google Scholar]
  • Brown AM , Lindsey DT. 2013 . Infant color vision and color preferences: a tribute to Davida Teller. Vis. Neurosci. 30 : 5–6 243– 50 [Google Scholar]
  • Changizi MA , Zhang Q , Shimojo S. 2006 . Bare skin, blood and the evolution of primate colour vision. Biol. Lett. 2 : 2 217– 21 [Google Scholar]
  • Chien SHL , Bronson-Castain K , Palmer J , Teller DY 2006 . Lightness constancy in 4-month-old infants. Vis. Res. 46 : 13 2139– 48 [Google Scholar]
  • Clifford A , Franklin A , Davies IR , Holmes A. 2009 . Electrophysiological markers of categorical perception of color in 7-month old infants. Brain Cogn . 71 : 2 165– 72 [Google Scholar]
  • Clifford A , Witzel C , Chapman A , French G , Hodson R et al. 2014 . Memory colour in infancy?. Perception 43 : 151 (Abstr.) [Google Scholar]
  • Conway BR , Chatterjee S , Field GD , Horwitz GD , Johnson EN et al. 2010 . Advances in color science: from retina to behavior. J. Neurosci. 30 : 45 14955– 63 [Google Scholar]
  • Conway BR , Ratnasingam S , Jara-Ettinger J , Futrell R , Gibson E. 2020 . Communication efficiency of color naming across languages provides a new framework for the evolution of color terms. Cognition 195 : 104086 [Google Scholar]
  • Cranwell MB , Pearce B , Loveridge C , Hurlbert AC. 2015 . Performance on the Farnsworth-Munsell 100-hue test is significantly related to nonverbal IQ. Investig. Ophthalmol. Vis. Sci. 56 : 5 3171– 78 [Google Scholar]
  • Crognale MA. 2002 . Development, maturation, and aging of chromatic visual pathways: VEP results. J. Vis. 2 : 6 438– 50 [Google Scholar]
  • Dannemiller JL. 1989 . A test of color constancy in 9-and 20-week-old human infants following simulated illuminant changes. Dev. Psychol. 25 : 2 171– 84 [Google Scholar]
  • Dannemiller JL , Hanko SA. 1987 . A test of color constancy in 4-month-old human infants. J. Exp. Child. Psychol. 44 : 2 255– 67 [Google Scholar]
  • Davies I , Franklin A. 2002 . Categorical similarity may affect colour pop-out in infants after all. Br. J. Dev. Psychol. 20 : 2 185– 203 [Google Scholar]
  • Davis JT , Robertson E , Lew-Levy S , Neldner K , Kapitany R et al. 2021 . Cultural components of sex differences in color preference. Child Dev . 92 : 4 1574– 89 [Google Scholar]
  • Dobkins KR , Bosworth RG , McCleery JP. 2009 . Effects of gestational length, gender, postnatal age, and birth order on visual contrast sensitivity in infants. J. Vis. 9 : 10 19 [Google Scholar]
  • Drivonikou GV , Kay P , Regier T , Ivry RB , Gilbert AL et al. 2007 . Further evidence that Whorfian effects are stronger in the right visual field than the left. PNAS 104 : 3 1097– 1102 [Google Scholar]
  • Forbes SH , Plunkett K. 2019 . Infants show early comprehension of basic color words. Dev. Psychol. 55 : 2 240– 49 [Google Scholar]
  • Forbes SH , Plunkett K. 2020 . Linguistic and cultural variation in early color word learning. Child Dev . 91 : 1 28– 42 [Google Scholar]
  • Franklin A , Drivonikou GV , Bevis L , Davies IR , Kay P , Regier T. 2008a . Categorical perception of color is lateralized to the right hemisphere in infants, but to the left hemisphere in adults. PNAS 105 : 9 3221– 25 [Google Scholar]
  • Franklin A , Drivonikou GV , Clifford A , Kay P , Regier T , Davies IR. 2008b . Lateralization of categorical perception of color changes with color term acquisition. PNAS 105 : 47 18221– 25 [Google Scholar]
  • Franklin A , Pilling M , Davies I. 2005 . The nature of infant color categorization: evidence from eye movements on a target detection task. J. Exp. Child. Psychol. 91 : 3 227– 48 [Google Scholar]
  • Franklin A , Sowden P , Burley R , Notman L , Alder E. 2008c . Color perception in children with autism. J. Autism Dev. Disord. 38 : 10 1837– 47 [Google Scholar]
  • Franklin A , Sowden P , Notman L , Gonzalez-Dixon M , West D et al. 2010 . Reduced chromatic discrimination in children with autism spectrum disorders. Dev. Sci. 13 : 1 188– 200 [Google Scholar]
  • Fujita T , Yamasaki T , Kamio Y , Hirose S , Tobimatsu S. 2011 . Parvocellular pathway impairment in autism spectrum disorder: evidence from visual evoked potentials. Res. Autism Spectrum Disord. 5 : 1 277– 85 [Google Scholar]
  • Gegenfurtner KR , Rieger J. 2000 . Sensory and cognitive contributions of color to the recognition of natural scenes. Curr. Biol. 10 : 13 805– 8 [Google Scholar]
  • Gegenfurtner KR , Wichmann FA , Sharpe LT. 1998 . The contribution of color to visual memory in X-chromosome-linked dichromats. Vis. Res. 38 : 7 1041– 45 [Google Scholar]
  • Gibson E , Futrell R , Jara-Ettinger J , Mahowald K , Bergen L et al. 2017 . Color naming across languages reflects color use. PNAS 114 : 40 10785– 90 [Google Scholar]
  • Gilbert AL , Regier T , Kay P , Ivry RB. 2006 . Whorf hypothesis is supported in the right visual field but not the left. PNAS 103 : 2 489– 94 [Google Scholar]
  • Granrud CE. 2006 . Size constancy in infants: 4-month-olds' responses to physical versus retinal image size. J. Exp. Psychol. Hum. Percept. Perform. 32 : 6 1398– 404 [Google Scholar]
  • Granrud CE. 2009 . Development of size constancy in children: a test of the metacognitive theory. Atten. Percept. Psychophys . 71 : 3 644– 54 [Google Scholar]
  • Granrud CE , Schmechel TT. 2006 . Development of size constancy in children: a test of the proximal mode sensitivity hypothesis. Percept. Psychophys. 68 : 8 1372– 81 [Google Scholar]
  • Grassivaro Gallo P , Oliva S , Lantieri P , Viviani F. 2002 . Colour blindness in Italian art high school students. Percept. Motor Skills 95 : 3 830– 34 [Google Scholar]
  • Heaton P , Ludlow A , Roberson D. 2008 . When less is more: poor discrimination but good colour memory in autism. Re s. Autism Spectrum Disord . 2 : 1 147– 56 [Google Scholar]
  • Hensch TK. 2005 . Critical period mechanisms in developing visual cortex. Curr. Top. Dev. Biol. 69 : 215– 37 [Google Scholar]
  • Houston-Price C , Nakai S 2004 . Distinguishing novelty and familiarity effects in infant preference procedures. Infant Child Dev . Int. J. Res. Pract . 13 : 4 341– 48 [Google Scholar]
  • Huebner GM , Shipworth DT , Gauthier S , Witzel C , Raynham P , Chan W 2016 . Saving energy with light? Experimental studies assessing the impact of colour temperature on thermal comfort. Energy Res. Soc. Sci. 15 : 45– 57 [Google Scholar]
  • Hurlbert AC , Ling Y. 2007 . Biological components of sex differences in color preference. Curr. Biol. 17 : 16 R623– 25 [Google Scholar]
  • Imai M , Saji N , Große G , Schulze C , Asano M , Saalbach H 2020 . General mechanisms of color lexicon acquisition: insights from comparison of German and Japanese speaking children. Proceedings of the 42nd Annual Conference of the Cognitive Science Society S Denison, M Mack, Y Xu, BC Armstrong 3315– 21 Austin, TX: Cogn. Sci. Soc. [Google Scholar]
  • Ishihara S , Ishihara M. 2016 . Ishihara's Design Charts for Colour Deficiency of Unlettered Persons Tokyo: Kanehara Trading [Google Scholar]
  • Jandó G , Mikó-Baráth E , Markó K , Hollódy K , Török B , Kovacs I. 2012 . Early-onset binocularity in preterm infants reveals experience-dependent visual development in humans. PNAS 109 : 27 11049– 52 [Google Scholar]
  • Johnson EK , McQueen JM , Huettig F. 2011 . Toddlers' language-mediated visual search: They need not have the words for it. Q. J. Exp. Psychol. 64 : 9 1672– 82 [Google Scholar]
  • Jonauskaite D , Abdel-Khalek AM , Abu-Akel A , Al-Rasheed AS , Antonietti JP et al. 2019 . The sun is no fun without rain: Physical environments affect how we feel about yellow across 55 countries. J. Environ. Psychol. 66 : 101350 [Google Scholar]
  • Káldy Z , Blaser E. 2009 . How to compare apples and oranges: infants' object identification tested with equally salient shape, luminance, and color changes. Infancy 14 : 2 222– 43 [Google Scholar]
  • Káldy Z , Leslie AM. 2003 . Identification of objects in 9-month-old infants: integrating “what” and “where” information. Dev. Sci. 6 : 3 360– 73 [Google Scholar]
  • Kay P , Berlin B , Maffi L , Merrifield WR , Cook R. 2009 . The World Color Survey Stanford, CA: CSLI Publ. [Google Scholar]
  • Kim S , Al-Haj M , Chen S , Fuller S , Jain U et al. 2014 . Colour vision in ADHD: part 1—testing the retinal dopaminergic hypothesis. Behav. Brain Funct. 10 : 38 [Google Scholar]
  • Kimura A , Wada Y , Yang J , Otsuka Y , Dan I et al. 2010 . Infants’ recognition of objects using canonical color. J. Exp. Child. Psychol. 105 : 3 256– 63 [Google Scholar]
  • Knoblauch K , Vital-Durand F , Barbur JL. 2001 . Variation of chromatic sensitivity across the life span. Vis. Res. 41 : 1 23– 36 [Google Scholar]
  • Knudsen EI. 2004 . Sensitive periods in the development of the brain and behavior. J. Cogn. Neurosci. 16 : 8 1412– 25 [Google Scholar]
  • Koh HC , Milne E , Dobkins K. 2010 . Contrast sensitivity for motion detection and direction discrimination in adolescents with autism spectrum disorders and their siblings. Neuropsychologia 48 : 14 4046– 56 [Google Scholar]
  • Kowalski K , Zimiles H. 2006 . The relation between children's conceptual functioning with color and color term acquisition. J. Exp. Child. Psychol. 94 : 4 301– 21 [Google Scholar]
  • Krentz UC , Earl RK. 2013 . The baby as beholder: Adults and infants have common preferences for original art. Psychol. Aesthet. Creativity Arts 7 : 2 181– 90 [Google Scholar]
  • Laeng B , Brennen T , Elden Å , Paulsen HG , Banerjee A , Lipton R. 2007 . Latitude-of-birth and season-of-birth effects on human color vision in the Arctic. Vis. Res. 47 : 12 1595– 607 [Google Scholar]
  • Lillo J , Moreira H , Alvaro L , Davies I 2014 . Use of basic color terms by red-green dichromats: 1. General description. Color Res. Appl. 39 : 4 360– 71 [Google Scholar]
  • Lindsey DT , Brown AM. 2021 . Lexical color categories. Annu. Rev. Vis. Sci. 7 : 605– 31 [Google Scholar]
  • Ling BY , Dain SJ. 2018 . Development of color vision discrimination during childhood: differences between Blue-Yellow, Red-Green, and achromatic thresholds. J. Opt. Soc. Am. A 35 : 4 B35– 42 [Google Scholar]
  • Ling Y , Hurlbert A. 2011 . Age-dependence of colour preference in the U.K. population. New Directions in Colour Studies CP Biggam, CA Hough, CJ Kay, DR Simmons 347– 60 Amsterdam: John Benjamins [Google Scholar]
  • Linhares JM , Nascimento SMC , Foster DH , Amano K. 2004 . Chromatic diversity of natural scenes. Perception 33 : 1 65 [Google Scholar]
  • LoBue V , DeLoache JS. 2011 . Pretty in pink: the early development of gender-stereotyped colour preferences. Br. J. Dev. Psychol. 29 : 3 656– 67 [Google Scholar]
  • Ludlow AK , Heaton P , Hill E , Franklin A 2014 . Color obsessions and phobias in autism spectrum disorders: the case of JG. Neurocase 20 : 3 296– 306 [Google Scholar]
  • Luo MR. 2006 . Applying colour science in colour design. Opt. Laser Technol. 38 : 4–6 392– 98 [Google Scholar]
  • Mani N , Johnson E , McQueen JM , Huettig F 2013 . How yellow is your banana? Toddlers' language-mediated visual search in referent-present tasks. Dev. Psychol. 49 : 6 1036– 44 [Google Scholar]
  • Mashige KP. 2019 . Impact of congenital color vision defect on color-related tasks among schoolchildren in Durban, South Africa. Clin. Optom. 4130 : 11 97– 102 [Google Scholar]
  • Maule J , Franklin A. 2019 . Color categorization in infants. Curr. Opin. Behav. Sci. 30 : 163– 68 [Google Scholar]
  • Maule J , Stanworth K , Pellicano E , Franklin A. 2017 . Ensemble perception of color in autistic adults. Autism Res 10 : 5 839– 51 [Google Scholar]
  • Maule J , Stanworth K , Pellicano E , Franklin A. 2018 . Color afterimages in autistic adults. J. Autism Dev. Disord. 48 : 4 1409– 21 [Google Scholar]
  • Maurer D , Werker JF. 2014 . Perceptual narrowing during infancy: a comparison of language and faces. Dev. Psychobiol. 56 : 2 154– 78 [Google Scholar]
  • McKyton A , Ben-Zion I , Doron R , Zohary E. 2015 . The limits of shape recognition following late emergence from blindness. Curr. Biol. 25 : 18 2373– 78 [Google Scholar]
  • Muris P , Meesters C , van den Berg F. 2003 . The Strengths and Difficulties Questionnaire (SDQ)–further evidence for its reliability and validity in a community sample of Dutch children and adolescents. Eur. Child Adolesc. Psychiatry 12 : 1– 8 [Google Scholar]
  • Nascimento SM , Albers AM , Gegenfurtner KR. 2021 . Naturalness and aesthetics of colors—preference for color compositions perceived as natural. Vis. Res. 185 : 98– 110 [Google Scholar]
  • Nascimento SM , Linhares JM , Montagner C , João CA , Amano K et al. 2017 . The colors of paintings and viewers’ preferences. Vis. Res. 130 : 76– 84 [Google Scholar]
  • Nithiyaananthan PJ , Kaur S , Anne BT , Eliana AN , Mahadir A. 2020 . Behavioural issues among primary schoolchildren with colour vision deficiency. IIUM Med. J. Malays. 19 : 3 37– 45 [Google Scholar]
  • Oliva A , Schyns PG. 2000 . Diagnostic colors mediate scene recognition. Cogn. Psychol. 41 : 2 176– 210 [Google Scholar]
  • Orenstein P. 2011 . Cinderella Ate My Daughter New York: HarperCollins [Google Scholar]
  • Osorio D , Vorobyev M. 1996 . Colour vision as an adaptation to frugivory in primates. Proc. R. Soc. Lond. B Biol. Sci. 263 : 1370 593– 99 [Google Scholar]
  • Ossenblok P , Reits D , Spekreijse H. 1992 . Analysis of striate activity underlying the pattern onset EP of children. Vis. Res. 32 : 10 1829– 35 [Google Scholar]
  • Palmer SE , Schloss KB. 2010 . An ecological valence theory of human color preference. PNAS 107 : 19 8877– 82 [Google Scholar]
  • Paramei GV , Oakley B. 2014 . Variation of color discrimination across the life span. J. Opt. Soc. Am. A 31 : 4 A375– 84 [Google Scholar]
  • Pellicano E , Burr D. 2012 . When the world becomes “too real”: a Bayesian explanation of autistic perception. Trends Cogn. Sci. 16 : 10 504– 10 [Google Scholar]
  • Peña M , Arias D , Dehaene-Lambertz G. 2014 . Gaze following is accelerated in healthy preterm infants. Psychol. Sci. 25 : 10 1884– 92 [Google Scholar]
  • Pereverzeva M , Chien SHL , Palmer J , Teller DY. 2002 . Infant photometry: Are mean adult isoluminance values a sufficient approximation to individual infant values?. Vis. Res. 42 : 13 1639– 49 [Google Scholar]
  • Peterzell DH , Werner JS , Kaplan PS. 1995 . Individual differences in contrast sensitivity functions: longitudinal study of 4-, 6- and 8-month-old human infants. Vis. Res. 35 : 7 961– 79 [Google Scholar]
  • Pitchaimuthu K , Sourav S , Bottari D , Banerjee S , Shareef I , Kekunnaya R , Röder B. 2019 . Color vision in sight recovery individuals. Restor. Neurol. Neurosci. 37 : 6 583– 90 [Google Scholar]
  • Pitchford NJ , Mullen KT. 2002 . Is the acquisition of basic-colour terms in young children constrained?. Perception 31 : 11 1349– 70 [Google Scholar]
  • Raskin LA , Maital S , Bornstein MH. 1983 . Perceptual categorization of color: a life-span study. Psychol. Res. 45 : 2 135– 45 [Google Scholar]
  • Regier T , Kay P , Cook RS. 2005 . Focal colors are universal after all. PNAS 102 : 23 8386– 91 [Google Scholar]
  • Rice M. 1980 . Cognition to Language: Categories, Word Meanings, and Training University Park, PA: Univ. Park Press [Google Scholar]
  • Rogers M , Franklin A , Knoblauch K. 2018 . A novel method to investigate how dimensions interact to inform perceptual salience in infancy. Infancy 23 : 6 833– 56 [Google Scholar]
  • Rogers M , Witzel C , Rhodes P , Franklin A. 2020 . Color constancy and color term knowledge are positively related during early childhood. J. Exp. Child. Psychol. 196 : 104825 [Google Scholar]
  • Rubin LR , Lackey WL , Kennedy FA , Stephenson RB. 2009 . Using color and grayscale images to teach histology to color-deficient medical students. Anat. Sci. Educ. 2 : 2 84– 88 [Google Scholar]
  • Saji N , Imai M , Asano M. 2020 . Acquisition of the meaning of the word orange requires understanding of the meanings of red, pink, and purple: constructing a lexicon as a connected system. Cogn. Sci. 44 : 1 e12813 [Google Scholar]
  • Samuelson LK , Horst JS. 2008 . Confronting complexity: insights from the details of behavior over multiple timescales. Dev. Sci. 11 : 2 209– 15 [Google Scholar]
  • Sandhofer CM , Smith LB. 1999 . Learning color words involves learning a system of mappings. Dev. Psychol. 35 : 3 668– 79 [Google Scholar]
  • Schloss KB , Lessard L , Racey C , Hurlbert AC. 2018a . Modeling color preference using color space metrics. Vis. Res. 151 : 99– 116 [Google Scholar]
  • Schloss KB , Lessard L , Walmsley CS , Foley K. 2018b . Color inference in visual communication: the meaning of colors in recycling. Cogn. Res. Princ. Implic. 3 : 5 [Google Scholar]
  • Schloss KB , Poggesi RM , Palmer SE. 2011 . Effects of university affiliation and “school spirit” on color preferences: Berkeley versus Stanford. Psychon. Bull. Rev. 18 : 3 498– 504 [Google Scholar]
  • Simmons DR , Robertson AE , McKay LS , Toal E , McAleer P , Pollick FE. 2009 . Vision in autism spectrum disorders. Vis. Res. 49 : 22 2705– 39 [Google Scholar]
  • Simoncelli EP , Olshausen BA. 2001 . Natural image statistics and neural representation. Annu. Rev. Neurosci. 24 : 1193– 216 [Google Scholar]
  • Siuda-Krzywicka K , Boros M , Bartolomeo P , Witzel C 2019 . The biological bases of colour categorisation: from goldfish to the human brain. Cortex 118 : 82– 106 [Google Scholar]
  • Skelton A , Catchpole G , Abbott J , Bosten J , Franklin A. 2017 . Biological origins of color categorization. PNAS 114 : 21 5545– 50 [Google Scholar]
  • Skelton AE , Franklin A. 2020 . Infants look longer at colours that adults like when colours are highly saturated. Psychon. Bull. Rev. 27 : 1 78– 85 [Google Scholar]
  • Skelton AE , Franklin A , Bosten J. 2022a . Colour vision is aligned with natural scene statistics at 4-months of age. bioRxiv 494927. https://doi.org/10.1101/2022.06.06.494927 [Crossref]
  • Skelton AE , MacInnes A , Panda K , Maule J , Bosten J et al. 2021 . Infants look longer at urban scenes than scenes of nature, and chromatic and spatial scene statistics can account for their looking Paper presented at the Lancaster Conference on Infant and Early Child Development Lancaster, UK: Aug 25– 27 [Google Scholar]
  • Skelton AE , Maule J , Franklin A. 2022b . Infant color perception: insight into perceptual development. Child Dev. Perspect. 16 : 90– 95 [Google Scholar]
  • Smithson HE. 2005 . Sensory, computational and cognitive components of human colour constancy. Philos. Trans. R. Soc. B Biol. Sci. 360 : 1458 1329– 46 [Google Scholar]
  • Sorokowski P , Sorokowska A , Witzel C. 2014 . Sex differences in color preferences transcend extreme differences in culture and ecology. Psychon. Bull. Rev. 21 : 5 1195– 201 [Google Scholar]
  • Spence C. 2015 . On the psychological impact of food colour. Flavour 4 : 21 [Google Scholar]
  • Stephen ID , Coetzee V , Law Smith M , Perrett DI 2009 . Skin blood perfusion and oxygenation colour affect perceived human health. PLOS ONE 4 : 4 e5083 [Google Scholar]
  • Suero MI , Pérez ÁL , Díaz F , Montanero M , Pardo PJ et al. 2005 . Does Daltonism influence young children's learning?. Learn. Individ. Diff. 15 : 2 89– 98 [Google Scholar]
  • Sugita Y. 2004 . Experience in early infancy is indispensable for color perception. Curr. Biol. 14 : 14 1267– 71 [Google Scholar]
  • Tagarelli A , Piro A , Tagarelli G , Lantieri PB , Risso D , Olivieri RL. 2004 . Colour blindness in everyday life and car driving. Acta Ophthalmol. Scand. 82 : 436– 42 [Google Scholar]
  • Tang T , Álvaro L , Alvarez J , Maule J , Skelton A et al. 2022 . ColourSpot, a novel gamified tablet-based test for accurate diagnosis of color vision deficiency in young children. Behav. Res. Methods 54 : 1148– 60 [Google Scholar]
  • Taylor C , Clifford A , Franklin A 2013a . Color preferences are not universal. J. Exp. Psychol. Gen. 142 : 4 1015– 27 [Google Scholar]
  • Taylor C , Franklin A. 2012 . The relationship between color-object associations and color preference: further investigation of ecological valence theory. Psychon. Bull. Rev. 19 : 2 190– 97 [Google Scholar]
  • Taylor C , Schloss K , Palmer SE , Franklin A. 2013b . Color preferences in infants and adults are different. Psychon. Bull. Rev. 20 : 5 916– 22 [Google Scholar]
  • Teller DY. 1998 . Spatial and temporal aspects of infant color vision. Vis. Res. 38 : 21 3275– 82 [Google Scholar]
  • Teller DY , Peeples DR , Sekel M. 1978 . Discrimination of chromatic from white light by two-month-old human infants. Vis. Res. 18 : 1 41– 48 [Google Scholar]
  • Tham DSY , Sowden PT , Grandison A , Franklin A , Lee AKW et al. 2020 . A systematic investigation of conceptual color associations. J. Exp. Psychol. Gen. 149 : 7 1311– 32 [Google Scholar]
  • Thomas BAWM , Kaur S , Hairol MI , Ahmad M , Wee LH. 2018 . Behavioural and emotional issues among primary school pupils with congenital colour vision deficiency in the Federal Territory of Kuala Lumpur, Malaysia: a case-control study. F1000Research 7 : 1834 [Google Scholar]
  • Torrents A , Bofill F , Cardona G. 2011 . Suitability of school textbooks for 5 to 7 year old children with colour vision deficiencies. Learn. Individ. Diff. 21 : 5 607– 12 [Google Scholar]
  • Tregillus KE , Isherwood ZJ , Vanston JE , Engel SA , MacLeod DI et al. 2021 . Color compensation in anomalous trichromats assessed with fMRI. Curr. Biol. 31 : 5 936– 42 [Google Scholar]
  • Uebel-von Sandersleben H , Albrecht B , Rothenberger A , Fillmer-Heise A , Roessner V et al. 2017 . Revisiting the co-existence of attention-deficit/hyperactivity disorder and chronic tic disorder in childhood—the case of colour discrimination, sustained attention and interference control. PLOS ONE 12 : 6 e0178866 [Google Scholar]
  • Wagner K , Dobkins K , Barner D. 2013 . Slow mapping: color word learning as a gradual inductive process. Cognition 127 : 3 307– 17 [Google Scholar]
  • Wagner K , Jergens J , Barner D. 2018 . Partial color word comprehension precedes production. Lang. Learn. Dev. 14 : 4 241– 61 [Google Scholar]
  • Wedge-Roberts RJ. 2021 . Colour constancy: cues, priors and development PhD Thesis Durham Univ. Durham, UK: [Google Scholar]
  • Wedge-Roberts RJ , Aston S , Kentridge R , Beierholm U , Nardini M , Olkkonen M. 2022 . Developmental changes in colour constancy in a naturalistic object selection task. Dev. Sci In press. https://doi.org/10.1111/desc.13306 [Crossref] [Google Scholar]
  • Werner JS , Marsh-Armstrong B , Knoblauch K. 2020 . Adaptive changes in color vision from long-term filter usage in anomalous but not normal trichromacy. Curr. Biol. 30 : 15 3011– 15 [Google Scholar]
  • Wichmann FA , Sharpe LT , Gegenfurtner KR. 2002 . The contributions of color to recognition memory for natural scenes. J. Exp. Psychol. Learn. Mem. Cogn. 28 : 3 509– 20 [Google Scholar]
  • Wilcox T. 1999 . Object individuation: infants’ use of shape, size, pattern, and color. Cognition 72 : 2 125– 66 [Google Scholar]
  • Wilcox T , Chapa C. 2004 . Priming infants to attend to color and pattern information in an individuation task. Cognition 90 : 3 265– 302 [Google Scholar]
  • Witzel C , Flack Z , Sanchez-Walker E , Franklin A 2021 . Colour category constancy and the development of colour naming. Vis. Res. 187 : 41– 54 [Google Scholar]
  • Witzel C , Gegenfurtner KR. 2011 . Is there a lateralized category effect for color?. J. Vis. 11 : 12 16 [Google Scholar]
  • Witzel C , Gegenfurtner KR. 2018 . Color perception: objects, constancy, and categories. Annu. Rev. Vis. Sci. 4 : 475– 99 [Google Scholar]
  • Wong WI , Hines M. 2015 . Effects of gender color-coding on toddlers’ gender-typical toy play. Arch. Sex. Behav. 44 : 5 1233– 42 [Google Scholar]
  • Yang J , Kanazawa S , Yamaguchi MK , Kuriki I. 2013 . Investigation of color constancy in 4.5-month-old infants under a strict control of luminance contrast for individual participants. . J. Exp. Child. Psychol. 115 : 1 126– 36 [Google Scholar]
  • Yang J , Kanazawa S , Yamaguchi MK , Kuriki I. 2016 . Cortical response to categorical color perception in infants investigated by near-infrared spectroscopy. PNAS 113 : 9 2370– 75 [Google Scholar]
  • Yokosawa K , Schloss KB , Asano M , Palmer SE. 2016 . Ecological effects in cross-cultural differences between US and Japanese color preferences. Cogn. Sci. 40 : 7 1590– 616 [Google Scholar]
  • Yurovsky D , Wagner K , Barner D , Frank MC 2015 . Signatures of domain-general categorization mechanisms in color word learning. Proceedings of the 37th Annual Conference of the Cognitive Science Society DC Noelle, R Dale, AS Warlaumont, J Yoshimi, T Matlock, et al. 2775– 80 Austin, TX: Cogn. Sci. Soc. [Google Scholar]
  • Zachi EC , Costa TL , Barboni MT , Costa MF , Bonci DM , Ventura DF. 2017 . Color vision losses in autism spectrum disorders. Front. Psychol. 8 : 1127 [Google Scholar]
  • Zemach I , Chang S , Teller DY 2007 . Infant color vision: prediction of infants’ spontaneous color preferences. Vis. Res. 47 : 10 1368– 81 [Google Scholar]

Data & Media loading...

  • Article Type: Review Article

Most Read This Month

Most cited most cited rss feed, job burnout, executive functions, social cognitive theory: an agentic perspective, on happiness and human potentials: a review of research on hedonic and eudaimonic well-being, sources of method bias in social science research and recommendations on how to control it, mediation analysis, missing data analysis: making it work in the real world, grounded cognition, personality structure: emergence of the five-factor model, motivational beliefs, values, and goals.

visual perception psychology research paper

Academia.edu no longer supports Internet Explorer.

To browse Academia.edu and the wider internet faster and more securely, please take a few seconds to  upgrade your browser .

  •  We're Hiring!
  •  Help Center

Visual perception

  • Most Cited Papers
  • Most Downloaded Papers
  • Newest Papers
  • Last »
  • Perception Follow Following
  • Visual attention Follow Following
  • Vision Science Follow Following
  • Cognitive Science Follow Following
  • Philosophy of perception Follow Following
  • Cognitive Neuroscience Follow Following
  • Attention Follow Following
  • Cognitive Psychology Follow Following
  • Consciousness Follow Following
  • Philosophy of Mind Follow Following

Enter the email address you signed up with and we'll email you a reset link.

  • Academia.edu Publishing
  •   We're Hiring!
  •   Help Center
  • Find new research papers in:
  • Health Sciences
  • Earth Sciences
  • Cognitive Science
  • Mathematics
  • Computer Science
  • Academia ©2024

Information

  • Author Services

Initiatives

You are accessing a machine-readable page. In order to be human-readable, please install an RSS reader.

All articles published by MDPI are made immediately available worldwide under an open access license. No special permission is required to reuse all or part of the article published by MDPI, including figures and tables. For articles published under an open access Creative Common CC BY license, any part of the article may be reused without permission provided that the original article is clearly cited. For more information, please refer to https://www.mdpi.com/openaccess .

Feature papers represent the most advanced research with significant potential for high impact in the field. A Feature Paper should be a substantial original Article that involves several techniques or approaches, provides an outlook for future research directions and describes possible research applications.

Feature papers are submitted upon individual invitation or recommendation by the scientific editors and must receive positive feedback from the reviewers.

Editor’s Choice articles are based on recommendations by the scientific editors of MDPI journals from around the world. Editors select a small number of articles recently published in the journal that they believe will be particularly interesting to readers, or important in the respective research area. The aim is to provide a snapshot of some of the most exciting work published in the various research areas of the journal.

Original Submission Date Received: .

  • Active Journals
  • Find a Journal
  • Proceedings Series
  • For Authors
  • For Reviewers
  • For Editors
  • For Librarians
  • For Publishers
  • For Societies
  • For Conference Organizers
  • Open Access Policy
  • Institutional Open Access Program
  • Special Issues Guidelines
  • Editorial Process
  • Research and Publication Ethics
  • Article Processing Charges
  • Testimonials
  • Preprints.org
  • SciProfiles
  • Encyclopedia

buildings-logo

Article Menu

visual perception psychology research paper

  • Subscribe SciFeed
  • Recommended Articles
  • Google Scholar
  • on Google Scholar
  • Table of Contents

Find support for a specific problem in the support section of our website.

Please let us know what you think of our products and services.

Visit our dedicated information section to learn more about MDPI.

JSmol Viewer

Emotional design and validation study of human–landscape visual interaction.

visual perception psychology research paper

Share and Cite

Ren, H.; Cheng, L.; Zhang, J.; Wang, Q.; Zhang, L. Emotional Design and Validation Study of Human–Landscape Visual Interaction. Buildings 2024 , 14 , 1966. https://doi.org/10.3390/buildings14071966

Ren H, Cheng L, Zhang J, Wang Q, Zhang L. Emotional Design and Validation Study of Human–Landscape Visual Interaction. Buildings . 2024; 14(7):1966. https://doi.org/10.3390/buildings14071966

Ren, Hongguo, Lu Cheng, Jing Zhang, Qingqin Wang, and Lujia Zhang. 2024. "Emotional Design and Validation Study of Human–Landscape Visual Interaction" Buildings 14, no. 7: 1966. https://doi.org/10.3390/buildings14071966

Article Metrics

Article access statistics, further information, mdpi initiatives, follow mdpi.

MDPI

Subscribe to receive issue release notifications and newsletters from MDPI journals

IMAGES

  1. (PDF) "Visual Perception: An Overview."

    visual perception psychology research paper

  2. Perception Research Paper Instruction

    visual perception psychology research paper

  3. Art and visual perception: a psychology of the creative eye Free Essay

    visual perception psychology research paper

  4. What Is Visual Perception In Psychology?

    visual perception psychology research paper

  5. Perception (Psychology): 10 Examples and Definition (2024)

    visual perception psychology research paper

  6. Research Paper: Psychology & Visual Design; The Role of Attention, Pe…

    visual perception psychology research paper

VIDEO

  1. Cognitive Psychology Research Paper Presentation

  2. Types of Perception

  3. Unlocking the Power of Psychology Essays

  4. PERCEPTION || PRINCIPLES OF PERCEPTION || ERRORS OF PERCEPTION || FACTORS AFFECTING PERCEPTION

  5. How Your Appearance Affects What People Think of You

  6. List of effects in Psychology

COMMENTS

  1. A Century of Gestalt Psychology in Visual Perception I. Perceptual Grouping and Figure-Ground Organization

    1 Introduction. Exactly 100 years ago Wertheimer (1912) published his paper on phi motion—perception of pure motion, without object motion—which many consider to be the beginning of Gestalt psychology as an important school of thought. The present status of Gestalt psychology is ambiguous. On the one hand, many psychologists believe that the Gestalt school died with its founding fathers in ...

  2. Form and Function in Information for Visual Perception

    Abstract. Visual perception involves spatially and temporally coordinated variations in diverse physical systems: environmental surfaces and symbols, optical images, electro-chemical activity in neural networks, muscles, and bodily movements—each with a distinctly different material structure and energy. The fundamental problem in the theory ...

  3. A century of Gestalt psychology in visual perception: I. Perceptual

    A century of Gestalt psychology in visual perception: I. Perceptual grouping and figure-ground organization ... Max Wertheimer published his paper on phi motion, widely recognized as the start of Gestalt psychology. ... we discuss its empirical and conceptual problems, and indicate how they are addressed in contemporary research on perceptual ...

  4. What visual perception tells us about mind and brain

    Recent studies of visual perception have begun to reveal the connection between neuronal activity in the brain and conscious visual experience. ... Neuroscience research over the past 40 years has revealed that there are roughly 30 different visual areas in ... This paper is a summary of a session presented at the third annual Japanese ...

  5. The human imagination: the cognitive neuroscience of visual mental

    However, evidence from the past 100 years of behavioural research suggests that visual imagery can have a functional effect on sensory processing akin to a weak form of visual perception 3.

  6. PDF A century of Gestalt psychology in visual perception: II. Conceptual

    perception and the rest of psychology. In our first article on the occasion of 100 years of Gestalt psychology (Wagemans et al., 2012), we demonstrated how some of these shortcomings were already alleviated in more contemporary research, performed in the Gestalt spirit, on perceptual grouping and figure ground or-ganization.

  7. Visual art history and the psychology of perception: Perspectivism and

    Because this visual pattern is a to features of the environment taken in relation to the position of the perceiver, art historian Edgerton rightly states, "there is nothing in original perspectiva theory [i.e., natural perspective] that had anything to do with the visual arts" (p. 22).That is, we are not referring here to a technique for transforming the appearance of the environment onto ...

  8. PDF A Survey of Perception-Based Visualization Studies by Task

    perception and its incorporation to visualization are derived from psychology-related journals, such as the Journal of Vi-sion, Attention, Perception, and Psychophysics, and Psycho-nomic. With the survey's objective and the vast availability of perception-based papers, it was challenging to perform a comprehensive literature search.

  9. Visual Perception

    B.G. Breitmeyer, in Encyclopedia of Consciousness, 2009. Visual perception is the registration of stimuli in phenomenal consciousness. An unperceived stimulus can leave traces at unconscious levels of processing that can affect the visual perception and performance.

  10. Visual Perception Based on Gestalt Theory

    Visual cognition is an important perceptual component of human cognitive system used to express and understand the environment. As the most important sense organ, human visual system has evolved for millions of years, allowing human to recognize and track objects visually [ 3 ]. In Gestalt theory, the law of proximity refers to the perception ...

  11. Different Mechanisms for Supporting Mental Imagery and Perceptual

    Recent research suggests imagery is functionally equivalent to a weak form of visual perception. Here we report evidence across five independent experiments on adults that perception and imagery are supported by fundamentally different mechanisms: Whereas perceptual representations are largely formed via increases in excitatory activity, imagery representations are largely supported by ...

  12. Visual Perception: Theoretical and Methodological Foundations

    In book: Experimental Psychology. Volume 4 in Weiner IB (Editor-in-Chief) Handbook of Psychology (pp.85-119) Edition: 2e; Chapter: Visual Perception: Theoretical and Methodological Foundations

  13. Vision

    For this Special Issue on "Visual Perception and Its Neural Mechanisms", we invite a mixture of original and review articles that provide insight into the neural computations performed by visual cortex. We especially encourage articles that address issues pertaining to (i) advances in techniques for neural measurement or (ii) neural data ...

  14. The Use of Virtual Reality in Psychology: A Case Study in Visual Perception

    In this paper we provide a brief overview of the benefits and challenges associated with VR in psychology research and discuss its utility in relation to the examination of visual perception. The term VR is often used interchangeably to refer to one of three types of system: a virtual environment presented on a flat screen, a room-based system ...

  15. Seeing What You Feel: Affect Drives Visual Perception of Structurally

    Abstract. Affective realism, the phenomenon whereby affect is integrated into an individual's experience of the world, is a normal consequence of how the brain processes sensory information from the external world in the context of sensations from the body. In the present investigation, we provided compelling empirical evidence that affective ...

  16. (PDF) Attention and Perception

    The Psychology of Attention presents a systematic review of the main lines of research on attention; the topics range from perception of threshold stimuli to memory storage and decisionmaking.

  17. Form and Function in Information for Visual Perception

    Abstract. Visual perception involves spatially and temporally coordinated variations in diverse physical systems: environmental surfaces and symbols, optical images, electro-chemical activity in neural networks, muscles, and bodily movements—each with a distinctly different material structure and energy. The fundamental problem in the theory ...

  18. Visual perception (Psychology) Research Papers

    Since there is limited experimental research on colour perception within healing environments, this research paper considers only a handful of experimental studies that specifically focus on patient colour preference and the physiological effects of colour within patient rooms in healthcare facilities; a designed/controlled environment where ...

  19. (PDF) A Century of Gestalt Psychology in Visual Perception: I

    In 1912, Max Wertheimer published his paper on phi motion, widely recognized as the start of Gestalt psychology. Because of its continued relevance in modern psychology, this centennial ...

  20. Visual Perception Theory In Psychology

    Summary. A lot of information reaches the eye, but much is lost by the time it reaches the brain (Gregory estimates about 90% is lost). Therefore, the brain has to guess what a person sees based on past experiences. We actively construct our perception of reality. Richard Gregory proposed that perception involves a lot of hypothesis testing to ...

  21. (PDF) Learning from illusions: From perception studies ...

    Learning from illusions: From perception studies to perspective-taking interventions. May 2023. Neuroscience Research 195 (8) May 2023. 195 (8) DOI: 10.1016/j.neures.2023.05.003. Authors: Francois ...

  22. The Development of Color Perception and Cognition

    Color is a pervasive feature of our psychological experience, having a role in many aspects of human mind and behavior such as basic vision, scene perception, object recognition, aesthetics, and communication. Understanding how humans encode, perceive, talk about, and use color has been a major interdisciplinary effort. Here, we present the current state of knowledge on how color perception ...

  23. Visual perception Research Papers

    Enhanced visual functioning in autism: An ALE meta-analysis. Autistics often exhibit enhanced perceptual abilities when engaged in visual search, visual discrimination, and embedded figure detection. In similar fashion, while performing a range of perceptual or cognitive tasks, autistics display... more. Download.

  24. Emotional Design and Validation Study of Human-Landscape Visual Interaction

    The formal beauty of "objects" is the main focus of modern rural landscapes, ignoring human interaction with the environment and the emotional reflection in this behavioral process. It is unable to satisfy the emotional needs of younger people who aspire to a high-quality life in the rural environment. The research idea of this paper is 'first assessment—then design—then validation ...