Skip to main content Accessibility help

We use cookies to distinguish you from other users and to provide you with a better experience on our websites. Close this message to accept cookies or find out how to manage your cookie settings.

Close cookie message
×
Hostname: page-component-78c5997874-t5tsf Total loading time: 0 Render date: 2024-11-10T21:01:15.552Z Has data issue: false hasContentIssue false

15 - Temporal Mental Imagery

from Part II - Imagery-Based Forms of the Imagination

Published online by Cambridge University Press:  26 May 2020

By
Gerardo Viera  and
Bence Nanay
Edited by
Anna Abraham
Anna Abraham
Affiliation:
University of Georgia
Get access

Summary

Mental imagery is perceptual processing that is not triggered by corresponding sensory stimulation in the relevant sense modality. Temporal mental imagery is perceptual processing that is not triggered by temporally corresponding sensory stimulation in the relevant sense modality. We aim to show that temporal mental imagery plays an important role in explaining a number of diverse mental phenomena, from the thickness of temporal experience and the specious present to episodic memory and postdictive perception.

Keywords

Mental imagerytemporal experiencespecious presentepisodic memorypostdictive perceptionmultimodal mental imagery
Type
Chapter
Information
The Cambridge Handbook of the Imagination , pp. 227 - 240
Publisher: Cambridge University Press
Print publication year: 2020

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Alais, D., and Burr, D. (2003). The “Flash-Lag” Effect Occurs in Audition and Cross-Modally, Current Biology, 13(1), 59–63.CrossRefGoogle Scholar
Bakin, J., Nakayama, K., and Gilbert, C. (2000). Visual Responses in Monkey Areas V1 and V2 to Three-Dimensional Surface Configurations. Journal of Neuroscience, 20, 8188–8198.Google Scholar
Ban, H., Yamamoto, H., Hanakawa, T., et al. (2013). Topographic Representation of an Occluded Object and the Effects of Spatiotemporal Context in Human Early Visual Areas. Journal of Neuroscience, 33, 16992–17007.CrossRefGoogle ScholarPubMed
Beck, J. (2018). Marking the Perception-Cognition Boundary. Australasian Journal of Philosophy, 96, 319–334.CrossRefGoogle Scholar
Bullier, J. (2004). Communications between Cortical Areas of the Visual System. In Chalupa, L. M. and Werner, J. S. (eds.), The Visual Neurosciences. Cambridge, MA: MIT Press, 522–540.Google Scholar
Bushnell, B. N., Harding, P. J., Kosai, Y., and Pasupathy, A. (2011). Partial Occlusion Modulates Contour-Based Shape Encoding in Primate Area V4. Journal of Neuroscience, 31, 4012–4024.CrossRefGoogle ScholarPubMed
Cai, M., Stetson, C., Eagleman, D. M. (2012). A Neural Model for Temporal Order Judgments and their Active Recalibration: A Common Mechanism for Space and Time? Frontiers in Psychology, 3, 470.Google Scholar
Ekman, M., Kok, P., and de Lange, F. (2017). Time-Compressed Preplay of Anticipated Events in Human Primary Visual Cortex. Nature Communications, 8.Google Scholar
Emmanouil, T., and Ro, T. (2014). Amodal Completion of Unconsciously Presented Objects. Psychonomic Bulletin & Review, 21(5), 1188–1194.Google Scholar
Esterman, M., and Yantis, S. (2010). Perceptual Expectation Modulates Category-Selective Cortical Activity. Cerebral Cortex, 20, 1245–1253.Google Scholar
Fujisaki, W., Shimojo, S., Kashino, M., and Nishida, S. (2004). Recalibration of Audiovisual Simultaneity. Nature Neuroscience, 7, 773–778.CrossRefGoogle ScholarPubMed
Geldard, F. A., and Sherrick, C. E. (1972). The Cutaneous “Rabbit”: A Perceptual Illusion. Science, 178, 178–179.Google Scholar
Grice, H. P. (1961). The Causal Theory of Perception. Proceedings of the Aristotelian Society, Supplementary Volume, 35, 121–153.Google Scholar
Grill-Spector, K., and Malach, R. (2004). The Human Visual Cortex. Annual Review of Neuroscience, 27, 649–677.CrossRefGoogle ScholarPubMed
Grush, R. (2007). Time and Experience. In Muller, T (ed.), Philosophie der Zeit: Neue Analytische Ansatze. Frankfurt, Germany: Verlag Vittorio Klostermann.Google Scholar
Grush, R. (2005). Internal Models and the Construction of Time: Generalizing from State Estimation to Trajectory Estimation to Address Temporal Features of Perception, including Temporal Illusions. Journal of Neural Engineering, 2(3), S209–218.Google Scholar
Hazenberg, S. J., Jongsma, M. L. A., Koning, A., and van Lier, R. (2014). Differential Familiarity Effects in Amodal Completion: Support from Behavioral and Electrophysiological Measurements. Journal of Experimental Psychology: Human Perception and Performance, 40(2), 669–684.Google Scholar
Hedgé, J., Fang, F., Murray, S. O., and Kersten, D. (2008). Preferential Responses to Occluded Objects in the Human Visual Cortex. Journal of Vision, 8, 16–35.Google Scholar
Hoerl, C. (2009). Time and Tense in Perceptual Experience. Philosopher’s Imprint, 9(12).Google Scholar
James, W. (1890). The Principles of Psychology. In 2 volumes. New York, NY: Henry Holt and Company.Google Scholar
Komatsu, H. (2006). The Neural Mechanisms of Perceptual Filling-in. Nature Review Neuroscience, 7, 220–231.Google Scholar
Kosslyn, S. M., Behrmann, M., and Jeannerod, M. (1995a). The Cognitive Neuroscience of Mental Imagery. Neuropsychologia, 33, 1335–1344.Google Scholar
Kosslyn, S. M., Thompson, W. L., Kim, I. J., and Alpert, N. M. (1995b). Topographical Representations of Mental Images in Primary Visual Cortex. Nature, 378: 496–498.Google Scholar
Kösem, A., Gramfort, A., and van Wassenhove, V. (2014). Encoding of Event Timing in the Phase of Neural Oscillations. NeuroImage, 92, 274–284.Google Scholar
Kovacs, G., Vogels, R., and Orban, G. A. (1995). Selectivity of Macaque Inferior Temporal Neurons for Partially Occluded Shapes. Journal of Neuroscience, 15, 1984–1997.Google Scholar
Larsen, A., Madsen, K. H., Lund, T. E., and Bundesen, C. (2006). Images of Illusory Motion in Primary Visual Cortex. Journal of Cognitive Neuroscience, 18(7), 1174–1180.Google Scholar
Leaver, A. M., van Lare, J., Zielinski, B., Halpern, A. R., and Rauschecker, J. P. (2009). Brain Activation during Anticipation of Sound Sequences. Journal of Neuroscience, 29(8), 2477–2485.CrossRefGoogle ScholarPubMed
Lee, G. (2014a). Extensionalism, Atomism, and Continuity. In Oaklander, N (ed.), Debates in the Metaphysics of Time. London: Bloomsbury.Google Scholar
Lee, G. (2014b). Temporal Experience and the Temporal Structure of Experience. Philosopher’s Imprint 14(3).Google Scholar
Lee, S. H., Kwan, A. C., Zhang, S., et al. (2012). Activation of Specific Interneurons Improves V1 Feature Selectivity and Visual Perception. Nature, 488, 379–383.Google Scholar
Lee, T. S., and Nguyen, M. (2001). Dynamics of Subjective Contour Formation in the Early Visual Cortex. Proceedings of the National Academy of Sciences , 98(4), 1907–1911.Google Scholar
Lerner, Y., Harel, M., and Malach, R. (2004). Rapid Completion Effects in Human High-Order Visual Areas. NeuroImage, 21, 516–526.CrossRefGoogle ScholarPubMed
Muckli, L., Kohler, A., Kriegeskorte, N., and Singer, W. (2005). Primary Visual Cortex Activity Along the Apparent-Motion Trace Reflects Illusory Perception. PLoS Biology, 3(8), 1501–1510.CrossRefGoogle ScholarPubMed
Nanay, B. (2010). Perception and Imagination: Amodal Perception as Mental Imagery. Philosophical Studies, 150, 239–254.Google Scholar
Nanay, B. (2012). Perceptual Phenomenology. Philosophical Perspectives, 26, 235–246.Google Scholar
Nanay, B. (2018a). Multimodal Mental Imagery. Cortex, 105, 125–134.Google Scholar
Nanay, B. (2018b). The Importance of Amodal Completion in Everyday Perception. I-Perception. https://doi.org/10.1177/2041669518788887Google Scholar
Nanay, B. (Forthcoming). Seeing Things You Don’t See. Oxford, UK: Oxford University Press.Google Scholar
Page, J. W., Duhamel, P., and Crognale, M. A. (2011). ERP Evidence of Visualization at Early Stages of Visual Processing. Brain and Cognition, 75(2), 141–146.Google Scholar
Pan, Y., Chen, M., Yin, J., et al. (2012). Equivalent Representation of Real and Illusory Contours in Macaque V4. Journal of Neuroscience, 32, 6760–6770.CrossRefGoogle ScholarPubMed
Pearson, J., and Westbrook, F. (2015). Phantom Perception: Voluntary and Involuntary Nonretinal Vision. Trends in Cognitive Sciences, 19, 278–284.Google Scholar
Pearson, J., Naselaris, T., Holmes, E. A., and Kosslyn, S. M. (2015). Mental Imagery: Functional Mechanisms and Clinical Applications. Trends in Cognitive Sciences, 19, 590–602.Google Scholar
Phillips, B. (2019). The Shifting Boundary between Perception and Cognition. Noûs, 53, 316–346.Google Scholar
Phillips, I. (2010). Perceiving Temporal Properties. European Journal of Philosophy, 18(2), 176–202.CrossRefGoogle Scholar
Phillips, I. (2011). Perception and Iconic Memory: What Sperling Doesn’t Show. Mind & Language, 281–311. doi.org/10.1111/j.1468-0017.2011.01422.x.Google Scholar
Phillips, I. (2014). Experience of and in Time. Philosophy Compass, 9, 131–144.Google Scholar
Rauschenberger, R., Liu, T., Slotnick, S. D., and Yantis, S. (2006). Temporally Unfolding Neural Representation of Pictorial Occlusion. Psychological Science, 17, 358–364.Google Scholar
Rees, A., Green, G., and Kay, R. H. (1986). Steady-State Evoked Responses to Sinusoidally Amplitude-Modulated Sounds Recorded in Man. Hearing Research, 23( 2). 123–133.Google Scholar
Regan, D. (1966). Some Characteristics of Average Steady-State and Transient Responses Evoked by Modulated Light. Electroencephalography and Clinical Neurophysiology, 20(3), 238–248.Google Scholar
Rolls, E. T., and Tovee, M. J. (1994). Processing Speed in the Cerebral Cortex and the Neurophysiology of Visual Masking. Proceedings of the Royal Society: Biological Sciences, 257, 9–15.Google Scholar
Scherzer, T. R., and Ekroll, V. (2015). Partial Modal Completion under Occlusion: What do Modal and Amodal Percepts Represent? Journal of Vision, 15, 1–20.Google Scholar
Shepard, R. N. (1978). Mental Images. American Psychologist, 33, 125–137.Google Scholar
Shibata, K., Watanabe, T., Sasaki, Y., and Kawato, M. (2011). Perceptual Learning Incepted by Decoded fMRI Neurofeedback without Stimulus Presentation. Science, 334, 1413–1415.Google Scholar
Shimoji, S. (2014). Postdiction: Its Implications on Visual Awareness, Hindsight, and Sense of Agency. Frontiers in Psychology, 5, 196.Google Scholar
Slotnick, S. D., Thompson, W. L., and Kosslyn, S. M. (2005). Visual Mental Imagery Induces Retinotopically Organized Activation of Early Visual Areas. Cerebral Cortex, 15, 1570–1583.CrossRefGoogle ScholarPubMed
Smith, F. W., and Muckli, L. (2010). Nonstimulated Early Visual Areas Carry Information About Surrounding Context. PNAS, 107, 20099–20103.Google Scholar
Stekelenburg, J., Sugano, Y., and Vroomen, J. (2011). Neural Correlates of Motor-Sensory Temporal Recalibration. Brain Research, 1397, 46–54.Google Scholar
Sterzer, P., Haynes, J. D., and Rees, G. (2006). Primary Visual Cortex Activation on the Path of Apparent Motion is Mediated by Feedback from hTM + V5. NeuroImage, 32, 1308–1316.Google Scholar
Stetson, C., Cui, X., Montague, P. R., and Eagleman, D. M. (2006). Motor-Sensory Recalibration Leads to an Illusory Reversal of Action and Sensation. Neuron, 51(5), 651–659.Google Scholar
Sugita, Y. (1999). Grouping of Image Fragments in Primary Visual Cortex. Nature, 401, 269–272.Google Scholar
Thorpe, S., Fize, D., and Marlot, C. (1996). Speed of Processing in the Human Visual System. Nature, 381, 520–522.Google Scholar
Viera, G. (2019). The Fragmentary Model of Temporal Experience and the Mirroring Constraint. Philosophical Studies, 176, 21.Google Scholar
Vroomen, J., Keetels, M., de Gelder, B., and Bertelson, P. (2004). Recalibration of Temporal Order Perception by Exposure to Audio–Visual Asynchrony. Cognitive Brain Research, 22, 32–35.Google Scholar
Vroomen, J., and Keetels, M. (2010). Perception of Intersensory Synchrony: A Tutorial Review. Attention, Perception, and Psychophysics, 72, 871–884.Google Scholar
Zatorre, R. J., and Halpern, A. R. (2005). Mental Concert: Musical Imagery and Auditory Cortex. Neuron, 47, 9–12.Google Scholar

Save book to Kindle

To save this book to your Kindle, first ensure coreplatform@cambridge.org is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

Available formats
×