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Suprathreshold asymmetries in human motion perception

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Abstract

Detection of asymmetries has been a mainstay of using vestibular reflexes to assess semicircular canal function. However, there has been relatively little work on how vestibular stimuli are perceived. Suprathreshold vestibular perception was measured in 13 normal healthy controls by having them compare the relative sizes of two yaw (vertical-axis rotation) or sway (right–left translation) stimuli. Both stimuli were 1.5 s in duration with a staircase used to adjust the relative size of the stimuli to find a pair of stimuli perceived as equal. Motion stimuli were delivered in darkness using a hexapod motion platform, and visual stimuli simulating motion were presented on a screen in the absence of platform motion. Both same direction (SD) and opposite direction (OD) stimuli were delivered in separate runs. After a two-interval stimulus, subjects reported which movement they perceived as larger. Cumulative distribution functions were fit to the responses so that the relative magnitudes of the two stimuli perceived as equal could be determined. For OD trial blocks, a directional asymmetry index was calculated to compare the relative size of perceived rightward and leftward motion. For all trial blocks, a temporal asymmetry index (TAI) was used to compare the relative size of the first and second intervals. Motion OD stimuli were perceived as equal in all subjects in yaw and all but one in sway. For visual OD stimuli, two subjects had slightly asymmetric responses for both sway and yaw. The TAI demonstrated asymmetry in 54 % in yaw, in which the second interval was perceived to be larger in all but one subject who had an asymmetry. For sway, only two subjects had a significant asymmetry. Visual stimuli produced a similar rate of asymmetry. The direction and magnitude of these asymmetries were not significantly correlated with those seen for motion stimuli. Asymmetries were found in a fraction with the TAI in SD stimuli for motion in yaw (42 %) and sway (33 %), as well as for vision in yaw (60 %) and sway (43 %). The precision at discriminating SD motion stimuli decreased significantly with age, but there was no difference in OD motion or visual stimuli.

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References

  • Addams R (1834) An account of a peculiar optical phenomenon seen after having looked at a moving body etc. Magaz J Sci. 3rd series 5:373–374

    Google Scholar 

  • Bárány R (1921) Diagnose von Krankheitserscheinungen im Bereiche des Otolithenapparates. Acta Otolaryngol 2:434–437

    Article  Google Scholar 

  • Benson AJ, Brown SF (1989) Visual display lowers detection threshold of angular, but not linear, whole-body motion stimuli. Aviat Space Environ Med 60:629–633

    PubMed  CAS  Google Scholar 

  • Benson AJ, Spencer MB, Stott JR (1986) Thresholds for the detection of the direction of whole-body, linear movement in the horizontal plane. Aviat Space Environ Med 57:1088–1096

    PubMed  CAS  Google Scholar 

  • Bertolini G, Ramat S, Laurens J, Bockisch CJ, Marti S, Straumann D, Palla A (2011) Velocity storage contribution to vestibular self-motion perception in healthy human subjects. J Neurophysiol 105:209–223. doi:10.1152/jn.00154.2010

    Article  PubMed  CAS  Google Scholar 

  • Bestelmeyer PE, Rouger J, DeBruine LM, Belin P (2010) Auditory adaptation in vocal affect perception. Cognition 117:217–223. doi:10.1016/j.cognition.2010.08.008

    Article  PubMed  Google Scholar 

  • Clark B (1967) Thresholds for the perception of angular acceleration in man. Aerosp Med 38:443–450

    PubMed  CAS  Google Scholar 

  • Crane BT (2012) Fore-aft translation after effects. Exp Brain Res (in press)

  • Crane BT, Demer JL (1998) Human horizontal vestibulo-ocular reflex initiation: effects of acceleration, target distance, and unilateral deafferentation. J Neurophysiol 80:1151–1166

    PubMed  CAS  Google Scholar 

  • Fetsch CR, Turner AH, Deangelis GC, Angelaki DE (2009) Dynamic re-weighting of visual and vestibular cues during self-motion perception. J Neurosci 29:15601–15612

    Article  PubMed  CAS  Google Scholar 

  • Gianna C, Heimbrand S, Gresty M (1996) Thresholds for detection of motion direction during passive lateral whole-body acceleration in normal subjects and patients with bilateral loss of labyrinthine function. Brain Res Bull 40:443–447; discussion 448-449

    Google Scholar 

  • Grabherr L, Nicoucar K, Mast FW, Merfeld DM (2008) Vestibular thresholds for yaw rotation about an earth-vertical axis as a function of frequency. Exp Brain Res 186:677–681

    Article  PubMed  Google Scholar 

  • Gundry AJ (1978) Thresholds of perception for periodic linear motion. Aviat Space Environ Med 49:679–686

    PubMed  CAS  Google Scholar 

  • Halmagyi GM, Curthoys IS (1988) A clinical sign of canal paresis. Arch Neurol 45:737–739

    Article  PubMed  CAS  Google Scholar 

  • Kanayama R, Bronstein AM, Gresty MA, Brookes GB, Faldon ME, Nakamura T (1995) Perceptual studies in patients with vestibular neurectomy. Acta Otolaryngol Suppl 520(Pt 2):408–411

    Article  PubMed  Google Scholar 

  • Kingma H (2005) Thresholds for perception of direction of linear acceleration as a possible evaluation of the otolith function. BMC Ear Nose Throat Disord 5:5

    Article  PubMed  CAS  Google Scholar 

  • Kohn A (2007) Visual adaptation: physiology, mechanisms, and functional benefits. J Neurophysiol 97:3155–3164. doi:10.1152/jn.00086.2007

    Article  PubMed  Google Scholar 

  • Levine SC, Glasscock M, McKennan KX (1990) Long-term results of labyrinthectomy. The Laryngoscope 100:125–127. doi:10.1288/00005537-199002000-00003

    PubMed  CAS  Google Scholar 

  • MacNeilage PR, Banks MS, DeAngelis GC, Angelaki DE (2010) Vestibular heading discrimination and sensitivity to linear acceleration in head and world coordinates. J Neurosci 30:9084–9094. doi:10.1523/JNEUROSCI.1304-10.2010

    PubMed  CAS  Google Scholar 

  • Mallery RM, Olomu OU, Uchanski RM, Militchin VA, Hullar TE (2010) Human discrimination of rotational velocities. Exp Brain Res. Experimentelle Hirnforschung. Experimentation cerebrale 204:11–20. doi:10.1007/s00221-010-2288-1

    Article  Google Scholar 

  • Melvill Jones GM, Young LR (1978) Subjective detection of vertical acceleration: a velocity-dependent response? Acta Otolaryngol 85:45–53

    Article  Google Scholar 

  • Merfeld DM (2011) Signal detection theory and vestibular thresholds: I. Basic theory and practical considerations. Exp Brain Res. Experimentelle Hirnforschung. Experimentation cerebrale. doi:10.1007/s00221-011-2557-7

    Google Scholar 

  • Merfeld DM, Park S, Gianna-Poulin C, Black FO, Wood S (2005a) Vestibular perception and action employ qualitatively different mechanisms. I. Frequency response of VOR and perceptual responses during translation and tilt. J Neurophysiol 94:186–198

    Article  PubMed  Google Scholar 

  • Merfeld DM, Park S, Gianna-Poulin C, Black FO, Wood S (2005b) Vestibular perception and action employ qualitatively different mechanisms. II. VOR and perceptual responses during combined Tilt&Translation. J Neurophysiol 94:199–205

    Article  PubMed  Google Scholar 

  • Perez N, Martin E, Garcia-Tapia R (2003) Dizziness: relating the severity of vertigo to the degree of handicap by measuring vestibular impairment. Otolaryngol Head Neck Surg 128:372–381

    Article  PubMed  Google Scholar 

  • Reinhardt-Rutland AH (1998) Increasing-loudness aftereffect following decreasing-intensity adaptation: spectral dependence in interotic and monotic testing. Perception 27:473–482

    Article  PubMed  CAS  Google Scholar 

  • Roditi RE, Crane BT (2011) Asymmetries in human vestibular perception thresholds. In: Association for research in Otolarngology, 34th annual meeting, Baltimore, MD, p 1006

  • Roditi RE, Crane BT (2012) Directional asymmetries and age effects in human self-motion perception. J Assoc Res Otolaryngol (in press)

  • Seizova-Cajic T, Smith JL, Taylor JL, Gandevia SC (2007) Proprioceptive movement illusions due to prolonged stimulation: reversals and aftereffects. PLoS ONE 2:e1037. doi:10.1371/journal.pone.0001037

    Article  PubMed  Google Scholar 

  • Soyka F, Robuffo Giordano P, Beykirch K, Bulthoff HH (2011) Predicting direction detection thresholds for arbitrary translational acceleration profiles in the horizontal plane. Exp Brain Res. Experimentelle Hirnforschung. Experimentation cerebrale 209:95–107. doi:10.1007/s00221-010-2523-9

    Article  Google Scholar 

  • Stefansson S, Imoto T (1986) Age-related changes in optokinetic and rotational tests. Am J Otol 7:193–196

    PubMed  CAS  Google Scholar 

  • Strupp M, Brandt T (2009) Vestibular neuritis. Semin Neurol 29:509–519. doi:10.1055/s-0029-1241040

    Article  PubMed  Google Scholar 

  • Thompson P, Burr D (2009) Visual aftereffects. Curr Biol CB 19:R11–R14. doi:10.1016/j.cub.2008.10.014

    Article  CAS  Google Scholar 

  • Tian JR, Shubayev I, Baloh RW, Demer JL (2001) Impairments in the initial horizontal vestibulo-ocular reflex of older humans. Exp Brain Res 137:309–322

    Article  PubMed  CAS  Google Scholar 

  • Walsh EG (1961) Role of the vestibular apparatus in the perception of motion on a parallel swing. J Physiol 155:506–513

    PubMed  CAS  Google Scholar 

  • Welgampola MS, Colebatch JG (2005) Characteristics and clinical applications of vestibular-evoked myogenic potentials. Neurology 64:1682–1688

    Article  PubMed  Google Scholar 

  • Wichmann FA, Hill NJ (2001a) The psychometric function: I. Fitting, sampling, and goodness of fit. Percept Psychophys 63:1293–1313

    Article  PubMed  CAS  Google Scholar 

  • Wichmann FA, Hill NJ (2001b) The psychometric function: II. Bootstrap-based confidence intervals and sampling. Percept Psychophys 63:1314–1329

    Article  PubMed  CAS  Google Scholar 

Download references

Acknowledgments

This study was funded by 1K23DC011298 from the NIDCD and a clinician-scientist award from the American Otological Society. We thank Justin Chan and Dan Stratz for providing technical support for this project.

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Correspondence to Benjamin T. Crane.

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Roditi, R.E., Crane, B.T. Suprathreshold asymmetries in human motion perception. Exp Brain Res 219, 369–379 (2012). https://doi.org/10.1007/s00221-012-3099-3

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