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The Uznadze illusion reveals similar effects of relative size on perception and action

  • Stefano UccelliEmail author
  • Veronica Pisu
  • Lucia Riggio
  • Nicola Bruno
Research Article

Abstract

Milner and Goodale (the visual brain in action, Oxford University Press Inc., Oxford, 1995) proposed a functional dissociation between vision-for-action and vision-for-perception (i.e., the “two-visual system hypothesis”, TVSH). Supporting the TVSH, it has been claimed that visual illusions affect perception but not actions. However, at least for the Ebbinghaus illusion, numerous studies have revealed consistent illusion effects on grasping. Thus, whether illusions affect actions remains controversial. To further investigate the dissociation predicted by the TVSH, we used a visual version of the Uznadze illusion (the same stimulus will feel smaller after feeling a larger stimulus and larger after feeling a smaller stimulus). Based on kinematic recordings of finger aperture in a motor (precision grip) and a perceptual task (manual estimation), we report two main findings. First, both action and perception are strongly affected by the Uznadze illusion. Second, the illusion decreases similarly in both tasks when inducing-induced pairs had different shape and color, in comparison to the equivalent condition where these features are the same. These results are inconsistent with a perception–action dissociation as predicted by the TVSH and suggest that, at least in the present conditions, vision-for-perception and vision-for-action are similarly affected by contextual cues.

Keywords

Perception Action Uznadze effect Grasping Similarity 

Notes

References

  1. Aglioti S, DeSouza JFX, Goodale MA (1995) Size-contrast deceive the eye but not the hand. Curr Biol 5(6):679–685CrossRefGoogle Scholar
  2. Biederman I (1987) Recognition-by-components: a theory of human image understanding. Psychol Rev 94:115–147CrossRefGoogle Scholar
  3. Bruno N (2001) When does actions resist visual illusions. Trends Cogn Sci 5(9):379–382CrossRefGoogle Scholar
  4. Bruno N (2016) Visual illusions in action. In: Shapiro A, Todorovic D (eds) The Oxford compendium of visual illusions. Oxford University Press, OxfordGoogle Scholar
  5. Bruno N, Franz VH (2009) When is grasping affected by the Müller-Lyer illusion? A quantitative review. Neuropsychologia 47:1421–1433CrossRefGoogle Scholar
  6. Bruno N, Bernardis P, Gentilucci M (2008) Visually guided pointing, the Müller-Lyer illusion, and the functional interpretation of the dorsal–ventral split: conclusions from 33 independent studies. Neurosci Biobehav Rev 32:423–437CrossRefGoogle Scholar
  7. Bruno N, Knox PC, de Grave DJ (2010) A metanalysis of the effect of the Müller-Lyer illusion on saccadic eye movements: no general support for a dissociation of perception and oculomotor action. Vis Res 50(24):2671–2682CrossRefGoogle Scholar
  8. Bruno N, Garofalo G, Daneyko O, Riggio L (2018) Visual similarity modulates visual size contrast. Acta Psychologica (Oxf) 188:122–130CrossRefGoogle Scholar
  9. Cardoso-Leite P, Gorea A (2010) On the perceptual/motor dissociation: a review of concepts, theory, experimental paradigms and data interpretations. Seeing Perceiving 23(2):89–151CrossRefGoogle Scholar
  10. Carey DP (2001) Do action systems resist visual illusion? Trends Cogn Sci 5(3):109–113CrossRefGoogle Scholar
  11. Daprati E, Gentilucci M (1997) Grasping an illusion. Neuropsychologia 35(12):1577–1582CrossRefGoogle Scholar
  12. Franz VH (2001) Action does not resist illusion. Trends Cogn Sci 5:11CrossRefGoogle Scholar
  13. Franz VH (2003) Manual size estimation: a neuropsychological measure of perception? Exp Brain Res 151:471–477CrossRefGoogle Scholar
  14. Franz VH, Gegenfurther RK (2008) Grasping visual illusions: consistent data and no dissociation. Cogn Neuropsychol 25(7–8):920–950CrossRefGoogle Scholar
  15. Franz VH, Gegenfurtner KR, Bülthoff HH, Fahle M (2000) Grasping visual illusions: no evidence for a dissociation between perception and action. Psychol Sci 11(1):20–25CrossRefGoogle Scholar
  16. Goodale MA (2008) Action without perception in human vision. Cogn Neuropsychol 25(7–8):891–919CrossRefGoogle Scholar
  17. Goodale MA (2011) Transforming vision into action. Vision Res 51(13):1567–1587CrossRefGoogle Scholar
  18. Goodale MA, Milner AD (1992) Separate visual pathways for perception and action. Trends Neurosci 15(1):20–25CrossRefGoogle Scholar
  19. Haffenden AM, Goodale MA (1998) The effect of pictorial illusion on prehension and perception. J Cogn Neurosci 10:122–136CrossRefGoogle Scholar
  20. Haffenden AM, Schiff KC, Goodale MA (2001) The dissociation between perception and action in the Ebbinghaus illusion: nonillusory effects of pictorial cues on grasp. Curr Biol 11:177–181CrossRefGoogle Scholar
  21. Kappers AML, Bergmann Tiest WM (2014) Influence of shape on the haptic size aftereffect. Plos One 9:1–8CrossRefGoogle Scholar
  22. Kopiske KK, Bruno N, Hesse C, Schenk T, Franz VH (2016) The functional subdivision of the visual brain: Is there a real illusion effect on action? A multi-lab replication study. Cortex 79:130–152CrossRefGoogle Scholar
  23. Leys C, Ley C, Klein O, Bernard P, Licata L (2013) Detecting outliers: Do not use standard deviation around the mean, use absolute deviation around the median. J Exp Soc Psychol 49(4):764–766CrossRefGoogle Scholar
  24. Loftus GR, Masson MEJ (1994) Using confidence intervals in within-subject designs. Psychon Bull Rev 1:476–490CrossRefGoogle Scholar
  25. McIntosh RD, Schenk T (2009) Two visual streams for perception and action: current trends. Neuropsychologia 47(6):1391–1396CrossRefGoogle Scholar
  26. Milner AD, Goodale MA (1995) The visual brain in action, 1st edn. Oxford University Press Inc., OxfordGoogle Scholar
  27. Milner AD, Goodale MA (2006) The visual brain in action, 2nd edn. Oxford University Press Inc., OxfordCrossRefGoogle Scholar
  28. Milner AD, Goodale MA (2008) Two visual systems reviewed. Neuropsychologia 46:774–785CrossRefGoogle Scholar
  29. Milner AD, Dijkerman HC, Pisella L, McIntosh RD, Tilikete C, Vighetto A, Rossetti Y (2001) Grasping the past: delay can improve visuomotor performance. Curr Biol 11:1896–1901CrossRefGoogle Scholar
  30. Milner AD, Ganel T, Goodale MA (2012) Does grasping in patient D.F. depend on vision? Trends Cogn Sci 16(5):256–257CrossRefGoogle Scholar
  31. Pavani F, Boscagli I, Benvenuti F, Rabuffetti M, Farnè A (1999) Are perception and illusion affected differently by the Titchener circles illusion? Exp Brain Res 127:95–101CrossRefGoogle Scholar
  32. Pisella L, Binfofski F, Lasek K, Toni I, Rossetti Y (2006) No double-dissociation between optic ataxia and visual agnosia: multiple sub-streams for multiple visuo-manual integrations. Neuropsychologia 44:2734–2748CrossRefGoogle Scholar
  33. Rossetti Y, Pisella L (2002) Several “vision for action” systems: a guide to dissociating and integrating dorsal and ventral functions. In: Prinz W, Hommel B (eds) Common mechanisms in perception and action: attention and performance, vol. XIX. Oxford University Press, Oxford, pp 375–396Google Scholar
  34. Rossetti Y, Pisella L, McIntosh RD (2017) Rise and fall of the two visual systems theory. Ann Phys Rehabil Med 60:130–140CrossRefGoogle Scholar
  35. Schenk T (2006) An allocentric rather than perceptual deficit in patient D.F. Nat Neurosci 9(11):13691370CrossRefGoogle Scholar
  36. Schenk T (2010) Visuomotor robustness is based on integration not segregation. Vision Res 50:2627–2632CrossRefGoogle Scholar
  37. Schenk T (2012) No dissociation between perception and action in patient DF when haptic feedback is withdrawn. J Neurosci 32(6):2013–2017CrossRefGoogle Scholar
  38. Schenk T, MacIntosh RD (2010) Do we have independent visual streams for perception and action? Cogn Neurosci 1(1):52–62CrossRefGoogle Scholar
  39. Schenk T, Franz VH, Bruno N (2011) Vision-for-perception and vision-for-action: which model is compatible with the available psychophysical and neuropsychological data? Vis Res 51:812–818CrossRefGoogle Scholar
  40. Smeets JBJ, Brenner E (1999) A new view on grasping. Mot Control 3(3):237–271CrossRefGoogle Scholar
  41. Smeets JBJ, Brenner E (2006) 10 Years of illusions. J Exp Psychol Hum Percept Perform 32(6):1501–1504CrossRefGoogle Scholar
  42. Stevens S (1957) On the psychophysical law. Psychol Rev 64(3):153–181CrossRefGoogle Scholar
  43. Ungerleider, Mishkin (1982) Contribution of striate inputs to the visuospatial functions of parieto-preoccipital cortex in monkeys. Behav Brain Res 6(1):57–77CrossRefGoogle Scholar
  44. Uznadze D (1966) The psychology of set. Consultants bureau, New YorkGoogle Scholar
  45. Whitwell RL, Milner AD, Goodale MA (2014) The two visual systems hypothesis: new challenges and insights from visual form agnosic patient DF. Front Neurol 5:255CrossRefGoogle Scholar
  46. Whitwell RL, Goodale MA (2016) Real and illusory issues in the illusion debate (why two things are sometimes better than one): commentary on Kopiske et al. (2016). Cortex.  https://doi.org/10.1523/JNEUROSCI.4748-07.2008 Google Scholar
  47. Whitwell RL, Goodale MA, Merritt KE, Enns JT (2018) The Sander parallelogram illusion dissociates action and perception despite control for the litany of past confounds. Cortex 98:163–176CrossRefGoogle Scholar
  48. Woodworth RS (1899) The accuracy of voluntary movement. Psychol Rev Monogr Suppl 3(3):i-114.  https://doi.org/10.1037/h0092992 Google Scholar

Copyright information

© Springer-Verlag GmbH Germany, part of Springer Nature 2019

Authors and Affiliations

  1. 1.Università di ParmaParmaItaly

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