Perceptual averaging governs antisaccade endpoint bias

Experimental Brain Research

Volumn 232, Issue 10, 2014, Pages 3201-3210

  Gillen, Caitlin ^a   Heath, Matthew ^a  

^a UNIVERSITY OF WESTERN ONTARIO   (Canada)

Author keywords

Antisaccade; Oculomotor; Perceptual averaging; Range effect

Indexed keywords

ADULT; ANTISACCADE; ARTICLE; AVERAGING; CONTROLLED STUDY; ECCENTRICITY; ENDPOINT BIAS; EYE MOVEMENT CONTROL; FEMALE; HUMAN; HUMAN EXPERIMENT; MALE; MATHEMATICAL PARAMETERS; NORMAL HUMAN; OCULOMOTOR SYSTEM; PERCEPTUAL AVERAGING; PROSACCADE; RESPONSE TIME; SACCADIC EYE MOVEMENT; STATISTICAL BIAS; VISION; VISUAL INFORMATION; VISUAL STIMULATION; EYE FIXATION; ORIENTATION; PHOTOSTIMULATION; PHYSIOLOGY; PROCEDURES; REACTION TIME; VISUAL FIELD; YOUNG ADULT;

ADULT; BIAS (EPIDEMIOLOGY); FEMALE; FIXATION, OCULAR; HUMANS; MALE; ORIENTATION; PHOTIC STIMULATION; REACTION TIME; SACCADES; VISUAL FIELDS; YOUNG ADULT;

EID: 84912000352     PISSN: 00144819     EISSN: 14321106     Source Type: Journal    
DOI: 10.1007/s00221-014-4010-1     Document Type: Article

References (55)

1. Abrams RA, Meyer DE, Kornblum S (1989) Speed and accuracy of saccadic eye movements: characteristics of impulse variability in the oculomotor system. J Exp Psychol Hum Percep Perf 15:529–543
2. Albrecht AR, Scholl BJ, Chun MM (2012) Perceptual averaging by eye and ear: computing summary statistics from multimodal stimuli. Atten Percept Psychophys 74:810–815
3. Ariely D (2001) Seeing sets: representation by statistical properties. Psychol Sci 12:157–162
4. Baird JC, Noma EJ (1978) Fundamentals of scaling and psychophysics. Wiley, New York
5. Becker W (1989) The neurobiology of saccadic eye movements. Metrics. Rev Oculomot Res 3:13–67
6. Becker W, Fuchs AF (1969) Further properties of the human saccadic system: eye movements and correction saccades with and without visual fixation points. Vis Res 9:1247–1258
7. Bell AH, Everling S, Munoz DP (2000) Influence of stimulus eccentricity and direction on characteristics of pro- and antisaccades in non-human primates. J Neurophysiol 84:2595–2604
8. Brainard DH (1997) The psychophysics toolbox. Spat Vis 10:433–436
9. Chong SC, Treisman A (2003) Representation of statistical properties. Vis Res 43:393–404
10. Cisek P (2007) Cortical mechanisms of action selection: the affordance competition hypothesis. Philos Trans R Soc Lond B Biol Sci 362:1585–1599
11. Corbett JE, Oriet C (2011) The whole is indeed more than the sum of its parts: perceptual averaging in the absence of individual item representation. Acta Psychol (Amst) 138:289–301
12. Cumming G (2013) Understanding the new statistics: effect sizes, confidence intervals, and meta-analysis. Routledge, New York
13. Dafoe JM, Armstrong IT, Munoz DP (2007) The influence of stimulus direction and eccentricity on pro- and anti-saccades in humans. Exp Brain Res 179:563–570
14. Davarpanah Jazi S, Heath M (2014) Weber’s law in tactile grasping and manual estimation: feedback-dependent evidence for functionally distinct processing streams. Brain Cogn 86:32–41
15. Deubel H, Wolf W, Hauske G (1986) Adaptive gain control of saccadic eye movements. Hum Neurobiol 5:245–253
16. Dorris MC, Olivier E, Munoz DP (2007) Competitive integration of visual and preparatory signals in the superior colliculus during saccadic programming. J Neurosci 27:5053–5062
17. Evdokimidis I, Tsekou H, Smyrnis N (2006) The mirror antisaccade task: direction-amplitude interaction and spatial accuracy characteristics. Exp Brain Res 174:304–311
18. Fischer B, Weber H (1992) Characteristics of “anti” saccades in man. Exp Brain Res 89:415–424
19. Gaveau V, Martin O, Prablanc C, Pélisson D, Urquizar C, Desmurget M (2003) On-line modification of saccadic eye movements by retinal signals. NeuroReport 14:875–878
20. Gerardin P, Gaveau V, Pélisson D, Prablanc C (2011) Integration of visual information for saccade production. Hum Mov Sci 30:1009–1021
21. Gillen C, Heath M (2014) Asymmetrical weighting of target eccentricities within a trial block influence antisaccade endpoint bias. Poster presented at the meeting of the Vision Sciences Society, St. Pete’s Beach, FL
22. Gillen C, Weiler J, Heath M (2013) Stimulus-driven saccades are characterized by an invariant undershooting bias: no evidence for a range effect. Exp Brain Res 230:165–174
23. Hallett PE (1978) Primary and secondary saccades to goals defined by instructions. Vis Res 18:1279–1296
24. Harris CM (1995) Does saccadic undershoot minimize saccadic flight-time? A Monte-Carlo study. Vis Res 35:691–701
25. Harris CM, Wolpert DM (1998) Signal-dependent noise determines motor planning. Nature 394:780–784
26. He PY, Kowler E (1989) The role of location probability in the programming of saccades: implications for “center-of-gravity” tendencies. Vis Res 29:1165–1181
27. Heath M (2005) Role of limb and target vision in the online control of memory-guided reaches. Mot Control 9:281–311
28. Heath M, Dunham K, Binsted G, Godbolt B (2010) Antisaccades exhibit diminished online control relative to prosaccades. Exp Brain Res 203:743–752
29. Heath M, Weiler J, Marriott K, Welsh TN (2011) Vector inversion diminishes the online control of antisaccades. Exp Brain Res 209:117–127
30. Kalesnykas RP, Hallett PE (1994) Retinal eccentricity and the latency of eye saccades. Vis Res 34:517–531
31. Kapoula Z (1985) Evidence for a range effect in the saccadic system. Vis Res 25:1155–1157
32. Kimmig H, Greenlee MW, Gondan M, Schira M, Kassubek J, Mergner T (2001) Relationship between saccadic eye movements and cortical activity as measured by fMRI: quantitative and qualitative aspects. Exp Brain Res 141:184–194
33. Knapp JM, Loomis JM (2004) Limited field of view of head-mounted displays is not the cause of distance underestimation in virtual environments. Presence Teleoper Virtual Environ 13:572–577
34. Kowler E, Blaser E (1995) The accuracy and precision of saccades to small and large targets. Vis Res 35:1741–1754
35. Krappmann P, Everling S, Flohr H (1998) Accuracy of visually and memory-guided antisaccades in man. Vis Res 38:2979–2985
36. Lemay M, Proteau L (2001) A distance effect in a manual aiming task to remembered targets: a test of three hypotheses. Exp Brain Res 140:357–368
37. Loftus GR, Masson ME (1994) Using confidence intervals in within-subject designs. Psychon Bull Rev 1:476–490
38. Moon SY, Barton JJ, Mikulski S, Polli FE, Cain MS, Vangel M, Hämäläinen MS, Manoach DS (2007) Where left becomes right: a magnetoencephalographic study of sensorimotor transformation for antisaccades. Neuroimage 36:1313–1323
39. Munoz DP, Everling S (2004) Look away: the anti-saccade task and the voluntary control of eye movement. Nat Rev Neurosci 5:218–228
40. Nyffeler T, Hartmann M, Hess CW, Müri RM (2008) Visual vector inversion during memory antisaccades—a TMS study. Prog Brain Res 171:429–432
41. Pedhazur EJ (1997) Multiple regression in behavioral research: explanation and prediction. Harcourt Brace College Publishers, Orlando
42. Poulton EC (1981) Human manual control. Comprehensive physiology. Wiley, New York
43. Prablanc C, Jeannerod M (1975) Corrective saccades: dependence on retinal reafferent signals. Vis Res 15:465–469
44. Robinson DA (1964) The mechanics of human saccadic eye movement. J Physiol 174:245–264
45. Robinson DA (1971) Models of oculomotor neural organization. In: Bach-y-Rita P, Collins C, Hyde JE (eds) The control of eye movements. Academic Press, New York, pp 515–538
46. Sheth BR, Shimojo S (2001) Compression of space in visual memory. Vis Res 41:329–341
47. Viguier A, Clément G, Trotter Y (2001) Distance perception within near visual space. Perception 30:115–124
48. Von Helmholtz H (1867) Handbuch der physiologischen optikoptical Society of America, reprinted 1962. Dover, New York
49. Walker R, Deubel H, Schneider WX, Findlay JM (1997) Effect of remote distractors on saccade programming: evidence for an extended fixation zone. J Neurophysiol 78:1108–1119
50. Weber RB, Daroff RB (1971) The metrics of horizontal saccadic eye movements in normal humans. Vis Res 11:921–928
51. Weiler J, Heath M (2012) The prior-antisaccade effect influences the planning and online control of prosaccades. Exp Brain Res 216:545–552
52. Weiler J, Heath M (2014) Repetitive antisaccade execution does not increase the unidirectional prosaccade switch-cost. Acta Psychol (Amst) 146:67–72
53. Westwood DA, Heath M, Roy EA (2003) No evidence for accurate visuomotor memory: systematic and variable error in memory-guided reaching. J Mot Behav 35:127–133
54. Wurtz RH, Albano JE (1980) Visual-motor function of the primate superior colliculus. Annu Rev Neurosci 3:189–226
55. Zhang M, Barash S (2000) Neuronal switching of sensorimotor transformations for antisaccades. Nature 408:971–975