The effect of stimulus strength on the speed and accuracy of a perceptual decision
Open accessAbstract
Both the speed and the accuracy of a perceptual judgment depend on the strength of the sensory stimulation. When stimulus strength is high, accuracy is high and response time is fast; when stimulus strength is low, accuracy is low and response time is slow. Although the psychometric function is well established as a tool for analyzing the relationship between accuracy and stimulus strength, the corresponding chronometric function for the relationship between response time and stimulus strength has not received as much consideration. In this article, we describe a theory of perceptual decision making based on a diffusion model. In it, a decision is based on the additive accumulation of sensory evidence over time to a bound. Combined with simple scaling assumptions, the proportional-rate and power-rate diffusion models predict simple analytic expressions for both the chronometric and psychometric functions. In a series of psychophysical experiments, we show that this theory accounts for response time and accuracy as a function of both stimulus strength and speed-accuracy instructions. In particular, the results demonstrate a close coupling between response time and accuracy. The theory is also shown to subsume the predictions of Piéron's Law, a power function dependence of response time on stimulus strength. The theory's analytic chronometric function allows one to extend theories of accuracy to response time.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Such an accumulation process explains both the choice and accuracy of decisions over a range of difficulty levels as well as the time required to make the decision.
“Such an accumulation process explains both the choice and accuracy of decisions over a range of difficulty levels as well as the time required to make the decision9.”
From Changes of mind in decision-making (2009) · cites this paper as [9]
The choice at initiation and reaction times as a function of task difficulty (coherence of dot motion) were explained by a bounded drift-diffusion model consistent with previous studies in humans and monkeys.
“The choice at initiation (initial hand trajectory) and reaction times as a function of task difficulty (coherence of dot motion) were explained by a bounded drift-diffusion model (Fig. 2, black curves) consistent with previous studies in humans and monkeys1,9,14.”
From Changes of mind in decision-making (2009) · cites this paper as [9]
The pattern of slower performance was explained by the same model with higher initiation bounds.
“The pattern was explained by the same model with higher initiation bounds9.”
From Changes of mind in decision-making (2009) · cites this paper as [9]
The model explains both the diminishing returns associated with prolonged viewing and the tradeoff between speed and accuracy in reaction time experiments.
“It explains both the diminishing returns associated with prolonged viewing in our experiment (Fig. S3) (20) and the tradeoff between speed and accuracy in reaction time experiments (13, 39, 40).”
From Representation of Confidence Associated with a Decision by Neurons in the Parietal Cortex (2009) · cites this paper as [39]
A formal model of bounded accumulation accounts quantitatively for subjects' speed and accuracy in 2-choice tasks.
“First, a formal model of bounded accumulation accounts quantitatively for subjects’ speed and accuracy3,6.”
From Decision-making with multiple alternatives (2008) · cites this paper as [3]
When human subjects perform the 2-choice motion task, they appear to adjust the bound (or excursion) when they trade off speed and accuracy.
“When human subjects perform the 2-choice motion task, they appear to adjust the bound (or excursion) when they trade off speed and accuracy3.”
From Decision-making with multiple alternatives (2008) · cites this paper as [3]
Analytic solutions exist for the probability of hitting bound A first and the mean time to bound A in the diffusion model.
“One advantage of this model is that analytic solutions exist for both of these22,49.”
From Microstimulation of macaque area LIP affects decision-making in a motion discrimination task (2006) · cites this paper as [22]
Cites
Brainard, D. H. (1997) · Spatial Vision · doi:10.1163/156856897x00357 · Cited by 19,308 · see citing works
The VideoToolbox software for visual psychophysics: transforming numbers into movies
Pelli, D. G. (1997) · Spatial Vision · doi:10.1163/156856897x00366 · Cited by 11,110 · see citing works
(1966) · Medical Entomology and Zoology · Cited by 10,293 · see citing works
Detection Theory: A User's Guide
Macmillan, N. A., & Creelman, C. D. (1991) · Cited by 5,415 · see citing works
Ratcliff, R. (1978) · Psychological Review · doi:10.1037/0033-295x.85.2.59 · Cited by 4,513 · see citing works
Ross, S. M. (1982) · Cited by 3,820 · see citing works
<i>The Theory of Stochastic Processes</i>
Cox, D. R., Miller, H. D., Weiss, G., & Shuler, K. (1966) · Physics Today · doi:10.1063/1.3047872 · Cited by 3,324 · see citing works
The time course of perceptual choice: The leaky, competing accumulator model.
Usher, M., & McClelland, J. L. (2001) · Psychological Review · doi:10.1037/0033-295x.108.3.550 · Cited by 2,152 · see citing works
Decision field theory: a dynamic-cognitive approach to decision making in an uncertain environment.
Busemeyer, J., & Townsend, J. (1993) · Psychology Review · doi:10.1037/0033-295x.100.3.432 · Cited by 2,000 · see citing works
The analysis of visual motion: a comparison of neuronal and psychophysical performance
Britten, K., Shadlen, M., Newsome, W., & Movshon, J. (1992) · The Journal of Neuroscience · doi:10.1523/jneurosci.12-12-04745.1992 · Cited by 1,958 · see citing works
Self-citationOn the speed of mental processes
Donders, F. C. (1969) · Acta Psychologica · doi:10.1016/0001-6918(69)90065-1 · Cited by 1,784 · see citing works
Neural Basis of a Perceptual Decision in the Parietal Cortex (Area LIP) of the Rhesus Monkey
Shadlen, M. N., & Newsome, W. T. (2001) · Journal of Neurophysiology · doi:10.1152/jn.2001.86.4.1916 · Cited by 1,755 · see citing works
Self-citationNeural correlates of decision variables in parietal cortex
Platt, M. L., & Glimcher, P. W. (1999) · Nature · doi:10.1038/22268 · Cited by 1,721 · see citing works
Roitman, J. D., & Shadlen, M. N. (2002) · The Journal of Neuroscience · doi:10.1523/jneurosci.22-21-09475.2002 · Cited by 1,589 · cited 3× · see citing works
“Data are from Roitman and Shadlen (2002). tion of the dots moved coherently in one of two possible directions while the others were randomly repositioned.”
BackgroundSelf-citationModeling Response Times for Two-Choice Decisions
Ratcliff, R., & Rouder, J. N. (1998) · Psychological Science · doi:10.1111/1467-9280.00067 · Cited by 1,478 · see citing works
A decision-making theory of visual detection.
Tanner, W. P., & Swets, J. A. (1954) · Psychological Review · doi:10.1037/h0058700 · Cited by 1,316 · see citing works
Speed-accuracy tradeoff and information processing dynamics
Wickelgren, W. A. (1977) · Acta Psychologica · doi:10.1016/0001-6918(77)90012-9 · Cited by 1,304 · see citing works
Watson, J. D. G., Myers, R., Frackowiak, R. S. J., Hajnal, J. V., Woods, R. P., Mazziotta, J. C., Shipp, S. D., & Zeki, S. (1993) · Cerebral Cortex · doi:10.1093/cercor/3.2.79 · Cited by 1,235 · see citing works
A Comparison of Sequential Sampling Models for Two-Choice Reaction Time.
Ratcliff, R., & Smith, P. L. (2004) · Psychological Review · doi:10.1037/0033-295x.111.2.333 · Cited by 1,227 · see citing works
Neural Control of Voluntary Movement Initiation
Hanes, D. P., & Schall, J. D. (1996) · Science · doi:10.1126/science.274.5286.427 · Cited by 1,145 · see citing works
Detection theory: A user's guide, 2nd ed.
Macmillan, N. A., & Creelman, C. D. (2005) · Cited by 1,117 · see citing works
Direction and orientation selectivity of neurons in visual area MT of the macaque
Albright, T. D. (1984) · Journal of Neurophysiology · doi:10.1152/jn.1984.52.6.1106 · Cited by 1,089 · see citing works
The Eyelink Toolbox: Eye tracking with MATLAB and the Psychophysics Toolbox
Cornelissen, F. W., Peters, E. M., & Palmer, J. C. (2002) · Behavior Research Methods, Instruments, & Computers · doi:10.3758/bf03195489 · Cited by 1,049 · see citing works
Self-citationAllport, A. (1989) · Cited by 1,016 · see citing works
Information theory of choice-reaction times
Laming, D. (1968) · Medical Entomology and Zoology · Cited by 952 · see citing works
Neural correlates of a decision in the dorsolateral prefrontal cortex of the macaque
Kim, J.-N., & Shadlen, M. N. (1999) · Nature Neuroscience · doi:10.1038/5739 · Cited by 950 · see citing works
Self-citationNeural computations that underlie decisions about sensory stimuli
Gold, J. I., & Shadlen, M. N. (2001) · Trends in Cognitive Sciences · doi:10.1016/s1364-6613(00)01567-9 · Cited by 881 · see citing works
Self-citationTemporal and spatial summation in human vision at different background intensities
Barlow, H. (1958) · Journal of Physiology · doi:10.1113/jphysiol.1958.sp005978 · Cited by 709 · see citing works
Models for choice-reaction time
Stone, M. (1960) · Psychometrika · doi:10.1007/bf02289729 · Cited by 696 · see citing works
A direct quantitative relationship between the functional properties of human and macaque V5
Rees, G. E., Friston, K. J., & Christof Koch, A. (2000) · Nature Neuroscience · doi:10.1038/76673 · Cited by 656 · see citing works
Probability summation over time.
Watson, A. (1979) · Vision Research · doi:10.1016/0042-6989(79)90136-6 · Cited by 626 · see citing works
Dubner, R. A., & Zeki, S. (1971) · Brain Research · doi:10.1016/0006-8993(71)90494-x · Cited by 625 · see citing works
A role for neural integrators in perceptual decision making
Mazurek, M. E., Roitman, J. D., Ditterich, J., & Shadlen, M. N. (2003) · Cerebral Cortex · doi:10.1093/cercor/bhg097 · Cited by 620 · see citing works
Self-citationRepresentation of a perceptual decision in developing oculomotor commands
Gold, J. I., & Shadlen, M. N. (2000) · Nature · doi:10.1038/35006062 · Cited by 616 · see citing works
Self-citationResponses of neurons in macaque MT to stochastic motion signals
Britten, K. H., Shadlen, M. N., Newsome, W. T., & Movshon, J. A. (1993) · Visual Neuroscience · doi:10.1017/s0952523800010269 · Cited by 594 · see citing works
Self-citationConnectionist and diffusion models of reaction time.
Ratcliff, R., Zandt, T. V., & McKoon, G. (1999) · Psychological Review · doi:10.1037/0033-295x.106.2.261 · Cited by 588 · see citing works
Flutter Discrimination: neural codes, perception, memory and decision making
Romo, R., & Salinas, E. (2003) · Nature reviews. Neuroscience · doi:10.1038/nrn1058 · Cited by 580 · see citing works
A Sequential Theory of Psychological Discrimination
Link, S. W., & Heath, R. A. (1975) · Psychometrika · doi:10.1007/bf02291481 · Cited by 492 · see citing works
Measuring, estimating, and understanding the psychometric function: A commentary
Klein, S. A. (2001) · Perception & Psychophysics · doi:10.3758/bf03194552 · Cited by 489 · see citing works
Ratcliff, R., Cherian, A., & Segraves, M. A. (2003) · Journal of Neurophysiology · doi:10.1152/jn.01049.2002 · Cited by 374 · see citing works
Pixel independence: measuring spatial interactions on a CRT display
Pelli, D. G. (1997) · Spatial Vision · doi:10.1163/156856897x00375 · Cited by 369 · see citing works
The Wave Theory of Difference and Similarity
Link, S. W. (2020) · Routledge eBooks · doi:10.1201/9780429054709 · Cited by 355 · see citing works
Ratcliff, R. (2002) · Psychonomic Bulletin & Review · doi:10.3758/bf03196283 · Cited by 339 · see citing works
Contrast detection and near-threshold discrimination in human vision
Foley, J. M., & Legge, G. E. (1981) · Vision Research · doi:10.1016/0042-6989(81)90009-2 · Cited by 294 · see citing works
Contrast discrimination in noise
Legge, G. E., Kersten, D., & Burgess, A. E. (1987) · Journal of the Optical Society of America A · doi:10.1364/josaa.4.000391 · Cited by 289 · see citing works
Heuristic filtering and reliable calibration methods for video-based pupil-tracking systems
Stampe, D. M. (1993) · Behavior Research Methods, Instruments, & Computers · doi:10.3758/bf03204486 · Cited by 288 · see citing works
Gold, J. I., & Shadlen, M. N. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-02-00632.2003 · Cited by 278 · see citing works
Self-citationStochastic Dynamic Models of Response Time and Accuracy: A Foundational Primer
Smith, P. L. (2000) · Journal of Mathematical Psychology · doi:10.1006/jmps.1999.1260 · Cited by 271 · see citing works
The relative judgment theory of two choice response time
Link, S. W. (1975) · Journal of Mathematical Psychology · doi:10.1016/0022-2496(75)90053-x · Cited by 251 · see citing works
A vector-magnitude model of contrast detection
Quick, R. (2004) · Kybernetik · doi:10.1007/bf00271628 · Cited by 248 · see citing works
A diffusion model account of masking in two-choice letter identification.
Ratcliff, R., & Rouder, J. N. (2000) · Journal of Experimental Psychology Human Perception & Performance · doi:10.1037//0096-1523.26.1.127 · Cited by 238 · see citing works
The accumulator model of two-choice discrimination
Smith, P. L., & Vickers, D. (1988) · Journal of Mathematical Psychology · doi:10.1016/0022-2496(88)90043-0 · Cited by 223 · see citing works
Introduction to Statistical Theory
Suxena, K. M. L. (1972) · Technometrics · doi:10.1080/00401706.1972.10488997 · Cited by 219 · see citing works
Psychophysically principled models of visual simple reaction time.
Smith, P. L. (1995) · Psychological Review · doi:10.1037/0033-295x.102.3.567 · Cited by 218 · see citing works
Accuracy, Information, and Response Time in a Saccadic Decision Task
Reddi, B. A. J., Asrress, K. N., & Carpenter, R. H. S. (2003) · Journal of Neurophysiology · doi:10.1152/jn.00689.2002 · Cited by 217 · see citing works
Pattern-motion responses in human visual cortex
Huk, A. C., & Heeger, D. J. (2001) · Nature Neuroscience · doi:10.1038/nn774 · Cited by 200 · see citing works
Self-citationTemporal and spatial integration in dynamic random-dot stimuli
Watamaniuk, S. N. J., & Sekuler, R. (1992) · Vision Research · doi:10.1016/0042-6989(92)90097-3 · Cited by 177 · see citing works
Horwitz, G. D., & Newsome, W. T. (2001) · Journal of Neurophysiology · doi:10.1152/jn.2001.86.5.2543 · Cited by 168 · see citing works
Temporal integration of optic flow, measured by contrast and coherence thresholds
Burr, D. C., & Santoro, L. (2001) · Vision Research · doi:10.1016/s0042-6989(01)00072-4 · Cited by 167 · see citing works
Do reaction time and accuracy measure the same aspects of letter recognition?
Santee, J. L., & Egeth, H. E. (1982) · Journal of Experimental Psychology Human Perception & Performance · doi:10.1037//0096-1523.8.4.489 · Cited by 162 · see citing works
Latency functions in human vision
Mansfield, R. J. W. (1973) · Vision Research · doi:10.1016/0042-6989(73)90224-1 · Cited by 150 · see citing works
Visual Detection and Discrimination of Luminance Increments*
Nachmias, J., & Kocher, E. C. (1970) · Journal of the Optical Society of America · doi:10.1364/josa.60.000382 · Cited by 149 · see citing works
Pins, D., & Bonnet, C. (1996) · Perception & Psychophysics · doi:10.3758/bf03206815 · Cited by 147 · see citing works
Smith, P. L., Ratcliff, R., & Wolfgang, B. J. (2004) · Vision Research · doi:10.1016/j.visres.2004.01.002 · Cited by 141 · see citing works
Evidence from auditory simple reaction times for both change and level detectors
Burbeck, S. L., & Luce, R. D. (1982) · Perception & Psychophysics · doi:10.3758/bf03204271 · Cited by 136 · see citing works
Limits to the temporal fidelity of cortical spike rate signals
Mazurek, M. E., & Shadlen, M. N. (2002) · Nature Neuroscience · doi:10.1038/nn836 · Cited by 131 · see citing works
Self-citationConditions for motion flow in dynamic visual noise
Morgan, M. J., & Ward, R. M. (1980) · Vision Research · doi:10.1016/0042-6989(80)90033-4 · Cited by 127 · see citing works
Visual detection of signals in the presence of continuous and pulsed backqrounds
Leshowitz, B. H., Tavb, H. B., & Raab, D. H. (1968) · Perception & Psychophysics · doi:10.3758/bf03206303 · Cited by 125 · see citing works
A note on modeling accumulation of information when the rate of accumulation changes over time
Ratcliff, R. (1980) · Journal of Mathematical Psychology · doi:10.1016/0022-2496(80)90006-1 · Cited by 112 · see citing works
Horwitz, G. D., & Newsome, W. T. (2001) · Journal of Neurophysiology · doi:10.1152/jn.2001.86.5.2527 · Cited by 88 · see citing works
Eckstein, M. P., & Whiting, J. S. (1996) · Journal of the Optical Society of America A · doi:10.1364/josaa.13.001777 · Cited by 84 · see citing works
Ideal observer for discrimination of the global direction of dynamic random-dot stimuli
Watamaniuk, S. N. J. (1993) · Journal of the Optical Society of America A · doi:10.1364/josaa.10.000016 · Cited by 80 · see citing works
The Time of Judgment in Psychometric Measures
Kellogg, W. N. (1931) · The American Journal of Psychology · doi:10.2307/1414239 · Cited by 71 · see citing works
On the relation between summation and facilitation
Pelli, D. G. (1987) · Vision Research · doi:10.1016/0042-6989(87)90148-9 · Cited by 53 · see citing works
A note on the distribution of response times for a random walk with Gaussian increments
Smith, P. L. (1990) · Journal of Mathematical Psychology · doi:10.1016/0022-2496(90)90023-3 · Cited by 51 · see citing works
A test of the deadline model for speed-accuracy tradeoffs
Ruthruff, E. (1996) · Perception & Psychophysics · doi:10.3758/bf03205475 · Cited by 41 · see citing works
Response time and accuracy revisited: Converging support for the interactive race model.
Mordkoff, J. T., & Egeth, H. E. (1993) · Journal of Experimental Psychology Human Perception & Performance · doi:10.1037//0096-1523.19.5.981 · Cited by 41 · see citing works
Single neurons and the perception of visual motion
Newsome, W. T., Britten, K. H., Movshon, J. A., & Shadlen, M. N. (1989) · Cited by 31 · see citing works
Self-citationThe relation between the velocity of visual motion and the reaction time to motion onset and offset
Hohnsbein, J., & Mateeff, S. (1992) · Vision Research · doi:10.1016/0042-6989(92)90173-g · Cited by 30 · see citing works
Bloch's law predictions from diffusion process models of detection
Smith, P. L. (1998) · Australian Journal of Psychology · doi:10.1080/00049539808258790 · Cited by 30 · see citing works
Choice reaction time with a random foreperiod
Green, D. M., Smith, A. F., & von Gierke, S. M. (1983) · Perception & Psychophysics · doi:10.3758/bf03202946 · Cited by 30 · see citing works
Burkhardt, D. A., Gottesman, J., & Keenan, R. M. (1987) · Journal of the Optical Society of America A · doi:10.1364/josaa.4.000530 · Cited by 28 · see citing works
Temporal summation of visual motion
Simpson, W. A. (1994) · Vision Research · doi:10.1016/0042-6989(94)90241-0 · Cited by 27 · see citing works
Pike, A. R. (1971) · Perception & Psychophysics · doi:10.3758/bf03208951 · Cited by 22 · see citing works
Multiple uses of visual motion. The case for stability in sensory cortex
Wezel, R. J. A. V., & Britten, K. H. (2002) · Neuroscience · doi:10.1016/s0306-4522(02)00036-2 · Cited by 20 · see citing works
Intensity and number of alternatives in hue identification: Piéron’s law and choice reaction time
Schweickert, R., Dahn, C., & McGuigan, K. (1988) · Perception & Psychophysics · doi:10.3758/bf03210422 · Cited by 20 · see citing works
A model of a single visual channel's response to weak test lights
Maloney, L. T., & Wandell, B. A. (1984) · Vision Research · doi:10.1016/0042-6989(84)90203-7 · Cited by 19 · see citing works
Reaction times to weak test lights
Wandell, B. A., Ahumada, P., & Welsh, D. K. (1984) · Vision Research · doi:10.1016/0042-6989(84)90205-0 · Cited by 12 · see citing works
Smith, P. L. (1994) · Journal of Mathematical Psychology · doi:10.1006/jmps.1994.1029 · Cited by 4 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
The Neural Basis of Decision Making
Gold, J. I., & Shadlen, M. N. (2007) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.29.051605.113038 · Cited by 3,764 · see citing works
Self-citationThe Diffusion Decision Model: Theory and Data for Two-Choice Decision Tasks
Ratcliff, R., & McKoon, G. (2008) · Neural Computation · doi:10.1162/neco.2008.12-06-420 · Cited by 3,059 · see citing works
Bogacz, R., Brown, E., Moehlis, J., Holmes, P. J., & Cohen, J. D. (2006) · Psychological Review · doi:10.1037/0033-295x.113.4.700 · Cited by 1,845 · see citing works
Diffusion decision model: Current issues and history
Ratcliff, R., Smith, P. L., Brown, S. D., & McKoon, G. (2016) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2016.01.007 · Cited by 1,630 · see citing works
“Diffusion and other models have been applied to many basic perceptual and memory tasks such as item and associative recognition [2,15,121,122,132], lexical decision [121,133], perceptual tasks including brightness, letter, motion, visual search, contrast, orientation discrimination tasks [7,14,16,44,103,104,134,135],…”
BackgroundMethodVisual fixations and the computation and comparison of value in simple choice
Krajbich, I., Armel, C., & Rangel, A. (2010) · Nature Neuroscience · doi:10.1038/nn.2635 · Cited by 1,408 · see citing works
A Recurrent Network Mechanism of Time Integration in Perceptual Decisions
Wong, K.-F., & Wang, X.-J. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.3733-05.2006 · Cited by 1,029 · see citing works
Representation of Confidence Associated with a Decision by Neurons in the Parietal Cortex
Kiani, R., & Shadlen, M. N. (2009) · Science · doi:10.1126/science.1169405 · Cited by 1,027 · see citing works
Self-citationChanges of mind in decision-making
Resulaj, A., Kiani, R., Wolpert, D. M., & Shadlen, M. N. (2009) · Nature · doi:10.1038/nature08275 · Cited by 678 · see citing works
Self-citationDecision-making with multiple alternatives
Churchland, A. K., Kiani, R., & Shadlen, M. N. (2008) · Nature Neuroscience · doi:10.1038/nn.2123 · Cited by 671 · see citing works
Self-citationEye movements: The past 25years
Kowler, E. (2011) · Vision Research · doi:10.1016/j.visres.2010.12.014 · Cited by 616 · see citing works
The Cost of Accumulating Evidence in Perceptual Decision Making
Drugowitsch, J., Moreno-Bote, R., Churchland, A. K., Shadlen, M. N., & Pouget, A. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.4010-11.2012 · Cited by 577 · see citing works
Self-citationAnticipated moments: temporal structure in attention
Nobre, A. C., & van Ede, F. (2017) · Nature reviews. Neuroscience · doi:10.1038/nrn.2017.141 · Cited by 573 · see citing works
An EZ-diffusion model for response time and accuracy
Wagenmakers, E., van der Maas, H. L. J., & Grasman, R. P. P. P. (2007) · Psychonomic Bulletin & Review · doi:10.3758/bf03194023 · Cited by 544 · see citing works
Brain plasticity through the life span: Learning to learn and action video games
Bavelier, D., Green, C. S., Pouget, A., & Schrater, P. (2012) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-060909-152832 · Cited by 541 · see citing works
Huk, A. C., & Shadlen, M. N. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.4684-04.2005 · Cited by 538 · see citing works
Self-citationIncreasing Speed of Processing With Action Video Games
Dye, M. W. G., Green, C. S., & Bavelier, D. (2009) · Current Directions in Psychological Science · doi:10.1111/j.1467-8721.2009.01660.x · Cited by 521 · see citing works
Cortico–basal ganglia circuit mechanism for a decision threshold in reaction time tasks
Lo, C.-C., & Wang, X.-J. (2006) · Nature Neuroscience · doi:10.1038/nn1722 · Cited by 505 · see citing works
Kiani, R., Hanks, T. D., & Shadlen, M. N. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.4761-07.2008 · Cited by 500 · see citing works
Self-citationChoice Certainty Is Informed by Both Evidence and Decision Time
Kiani, R., Corthell, L., & Shadlen, M. N. (2014) · Neuron · doi:10.1016/j.neuron.2014.12.015 · Cited by 470 · see citing works
Self-citationHow the brain integrates costs and benefits during decision making
Basten, U., Biele, G., Heekeren, H. R., & Fiebach, C. J. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0908104107 · Cited by 466 · see citing works
Bias in the Brain: A Diffusion Model Analysis of Prior Probability and Potential Payoff
Mulder, M., Wagenmakers, E., Ratcliff, R., Boekel, W., & Forstmann, B. U. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.4156-11.2012 · Cited by 427 · see citing works
Philiastides, M. G., Ratcliff, R., & Sajda, P. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.1655-06.2006 · Cited by 394 · see citing works
Heekeren, H. R., Marrett, S., Ruff, D. A., Bandettini, P. A., & Ungerleider, L. G. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0603949103 · Cited by 385 · see citing works
Elapsed Decision Time Affects the Weighting of Prior Probability in a Perceptual Decision Task
Hanks, T. D., Mazurek, M. E., Kiani, R., Hopp, E., & Shadlen, M. N. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.5613-10.2011 · Cited by 378 · see citing works
Self-citationThe classic P300 encodes a build‐to‐threshold decision variable
Twomey, D. M., Murphy, P. R., Kelly, S. P., & O'Connell, R. G. (2015) · European Journal of Neuroscience · doi:10.1111/ejn.12936 · Cited by 376 · see citing works
Microstimulation of macaque area LIP affects decision-making in a motion discrimination task
Hanks, T. D., Ditterich, J., & Shadlen, M. N. (2006) · Nature Neuroscience · doi:10.1038/nn1683 · Cited by 360 · see citing works
Self-citationImproved Probabilistic Inference as a General Learning Mechanism with Action Video Games
Green, C. S., Pouget, A., & Bavelier, D. (2010) · Current Biology · doi:10.1016/j.cub.2010.07.040 · Cited by 356 · see citing works
Corticostriatal neurons in auditory cortex drive decisions during auditory discrimination
Znamenskiy, P., & Zador, A. M. (2013) · Nature · doi:10.1038/nature12077 · Cited by 339 · see citing works
Time course of visual perception: Coarse-to-fine processing and beyond
HEGDE, J. (2007) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2007.09.001 · Cited by 328 · see citing works
Hierarchical diffusion models for two-choice response times.
Vandekerckhove, J., Tuerlinckx, F., & Lee, M. D. (2011) · Psychological Methods · doi:10.1037/a0021765 · Cited by 323 · see citing works
Milosavljevic, M., Malmaud, J., Huth, A. G., Christof Koch, A., & Rangel, A. (2010) · Judgment and Decision Making · doi:10.1017/s1930297500001285 · Cited by 320 · see citing works
Cravo, A. M., Rohenkohl, G., Wyart, V., & Nobre, A. C. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.4675-12.2013 · Cited by 304 · see citing works
Varying Target Prevalence Reveals Two Dissociable Decision Criteria in Visual Search
Wolfe, J. M., & Wert, M. J. V. (2010) · Current Biology · doi:10.1016/j.cub.2009.11.066 · Cited by 292 · see citing works
Revisiting the Evidence for Collapsing Boundaries and Urgency Signals in Perceptual Decision-Making
Hawkins, G. E., Forstmann, B. U., Wagenmakers, E., Ratcliff, R., & Brown, S. D. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.2410-14.2015 · Cited by 285 · see citing works
Caudate Encodes Multiple Computations for Perceptual Decisions
Ding, L., & Gold, J. I. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.2894-10.2010 · Cited by 284 · see citing works
Ploran, E. J., Nelson, S. M., Velanova, K., Donaldson, D. I., Petersen, S. E., & Wheeler, M. E. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.3522-07.2007 · Cited by 282 · see citing works
Temporal Expectation Improves the Quality of Sensory Information
Rohenkohl, G., Cravo, A. M., Wyart, V., & Nobre, A. C. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.0804-12.2012 · Cited by 273 · see citing works
Ding, L., & Gold, J. I. (2011) · Cerebral Cortex · doi:10.1093/cercor/bhr178 · Cited by 267 · see citing works
Decision making by urgency gating: theory and experimental support
Thura, D., Beauregard-Racine, J., Fradet, C.-W., & Cisek, P. (2012) · Journal of Neurophysiology · doi:10.1152/jn.01071.2011 · Cited by 267 · see citing works
Stochastic models of decisions about motion direction: Behavior and physiology
Ditterich, J. (2006) · Neural Networks · doi:10.1016/j.neunet.2006.05.042 · Cited by 233 · see citing works
Seeing at a glance, smelling in a whiff: rapid forms of perceptual decision making
Uchida, N., Kepecs, Á., & Mainen, Z. F. (2006) · Nature reviews. Neuroscience · doi:10.1038/nrn1933 · Cited by 231 · see citing works
Evidence for time‐variant decision making
Ditterich, J. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.05221.x · Cited by 229 · see citing works
Perceptual decision making in less than 30 milliseconds
Stanford, T. R., Shankar, S., Massoglia, D. P., Costello, M. G., & Salinas, E. (2010) · Nature Neuroscience · doi:10.1038/nn.2485 · Cited by 228 · see citing works
Simen, P., Contreras, D., Buck, C. L., Hu, P. T., Holmes, P. J., & Cohen, J. D. (2009) · Journal of Experimental Psychology Human Perception & Performance · doi:10.1037/a0016926 · Cited by 224 · see citing works
A neural mechanism of speed-accuracy tradeoff in macaque area LIP
Hanks, T., Kiani, R., & Shadlen, M. N. (2014) · eLife · doi:10.7554/elife.02260 · Cited by 222 · see citing works
Self-citationDowns, M. E., Buch, A., Sierra, C., Karakatsani, M. E., Chen, S., Konofagou, E. E., & Ferrera, V. P. (2015) · PLoS ONE · doi:10.1371/journal.pone.0125911 · Cited by 218 · see citing works
Perceptual decision neurosciences – A model-based review
Mulder, M., van Maanen, L., & Forstmann, B. U. (2014) · Neuroscience · doi:10.1016/j.neuroscience.2014.07.031 · Cited by 214 · see citing works
Multisensory Decision-Making in Rats and Humans
Raposo, D. C., Sheppard, J. P., Schrater, P., & Churchland, A. K. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.4998-11.2012 · Cited by 207 · see citing works
The Basal Ganglia’s Contributions to Perceptual Decision Making
Ding, L., & Gold, J. I. (2013) · Neuron · doi:10.1016/j.neuron.2013.07.042 · Cited by 201 · see citing works
Causal Role of Dorsolateral Prefrontal Cortex in Human Perceptual Decision Making
Philiastides, M. G., Auksztulewicz, R., Heekeren, H. R., & Blankenburg, F. (2011) · Current Biology · doi:10.1016/j.cub.2011.04.034 · Cited by 200 · see citing works
Decision-Related Activity in Sensory Neurons: Correlations Among Neurons and with Behavior
Nienborg, H., Cohen, M. R., & Cumming, B. G. (2012) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-062111-150403 · Cited by 199 · see citing works
Pupil-Linked Arousal Determines Variability in Perceptual Decision Making
Murphy, P. R., Vandekerckhove, J., & Nieuwenhuis, S. (2014) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1003854 · Cited by 197 · see citing works
Brain mechanisms for perceptual and reward-related decision-making
Deco, G., Rolls, E. T., Albantakis, L., & Romo, R. (2013) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2012.01.010 · Cited by 196 · see citing works
Global gain modulation generates time-dependent urgency during perceptual choice in humans
Murphy, P. R., Boonstra, E., & Nieuwenhuis, S. (2016) · Nature Communications · doi:10.1038/ncomms13526 · Cited by 196 · see citing works
Neural Correlates of Trial-to-Trial Fluctuations in Response Caution
van Maanen, L., Brown, S. D., Eichele, T., Wagenmakers, E., Ho, T. C., Serences, J. T., & Forstmann, B. U. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.2924-11.2011 · Cited by 191 · see citing works
Normative evidence accumulation in unpredictable environments
Glaze, C. M., Kable, J. W., & Gold, J. I. (2015) · eLife · doi:10.7554/elife.08825 · Cited by 190 · see citing works
Effects of cortical microstimulation on confidence in a perceptual decision
Fetsch, C. R., Kiani, R., Newsome, W. T., & Shadlen, M. N. (2014) · Neuron · doi:10.1016/j.neuron.2014.07.011 · Cited by 185 · see citing works
Self-citationMultimodal signals enhance decision making in foraging bumble-bees
Kulahci, I. G., Dornhaus, A., & Papaj, D. R. (2008) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2007.1176 · Cited by 185 · see citing works
Do humans produce the speed–accuracy trade-off that maximizes reward rate?
Bogacz, R., Hu, P. T., Holmes, P. J., & Cohen, J. D. (2009) · Quarterly Journal of Experimental Psychology · doi:10.1080/17470210903091643 · Cited by 179 · see citing works
What are the shapes of response time distributions in visual search?
Palmer, E. M., Horowitz, T. S., Torralba, A. B., & Wolfe, J. M. (2010) · Journal of Experimental Psychology Human Perception & Performance · doi:10.1037/a0020747 · Cited by 173 · see citing works
fMRI Evidence for a Dual Process Account of the Speed-Accuracy Tradeoff in Decision-Making
Ivanoff, J., Branning, P., & Marois, R. (2008) · PLoS ONE · doi:10.1371/journal.pone.0002635 · Cited by 168 · see citing works
Neural Correlates of Perceptual Choice and Decision Making during Fear–Disgust Discrimination
Thielscher, A., & Pessoa, L. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.3024-06.2007 · Cited by 168 · see citing works
Target selection in visual search as revealed by movement trajectories
Song, J., & Nakayama, K. (2008) · Vision Research · doi:10.1016/j.visres.2007.12.015 · Cited by 164 · see citing works
Representation of accumulating evidence for a decision in two parietal areas
de Lafuente, V., Jazayeri, M., & Shadlen, M. N. (2015) · The Journal of Neuroscience · doi:10.1523/jneurosci.2451-14.2015 · Cited by 162 · see citing works
“…and not about the plan of action used to communicate the choice, yet our decisions are governed by an evidence accumulation process similar to the one studied in monkeys (Smith and Ratcliff, 2004; Palmer et al., 2005; Philiastides et al., 2006; Green et al., 2012; O’Connell et al., 2012).”
ResultSelf-citationDisentangling decision models: From independence to competition.
Teodorescu, A. R., & Usher, M. (2013) · Psychological Review · doi:10.1037/a0030776 · Cited by 155 · see citing works
Similarity Effect and Optimal Control of Multiple-Choice Decision Making
Furman, M., & Wang, X. (2008) · Neuron · doi:10.1016/j.neuron.2008.12.003 · Cited by 143 · see citing works
Meister, M. L. R., Hennig, J. A., & Huk, A. C. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.2984-12.2013 · Cited by 143 · see citing works
Self-citationZylberberg, A. D., Fetsch, C. R., & Shadlen, M. N. (2016) · eLife · doi:10.7554/elife.17688 · Cited by 140 · see citing works
Self-citationThe opportunity cost of time modulates cognitive effort
Otto, A. R., & Daw, N. D. (2019) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2018.05.006 · Cited by 138 · see citing works
Beyond Trial-Based Paradigms: Continuous Behavior, Ongoing Neural Activity, and Natural Stimuli
Huk, A. C., Bonnen, K., & He, B. J. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.1920-17.2018 · Cited by 138 · see citing works
Self-citationNeural correlates of evidence accumulation in a perceptual decision task
Liu, T., & Pleskac, T. J. (2011) · Journal of Neurophysiology · doi:10.1152/jn.00413.2011 · Cited by 137 · see citing works
Roxin, A., & Ledberg, A. (2008) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1000046 · Cited by 135 · see citing works
Optimal multisensory decision-making in a reaction-time task
Drugowitsch, J., DeAngelis, G. C., Klier, E. M., Angelaki, D. E., & Pouget, A. (2014) · eLife · doi:10.7554/elife.03005 · Cited by 133 · see citing works
What a difference a parameter makes: A psychophysical comparison of random dot motion algorithms
Pilly, P. K., & Seitz, A. R. (2009) · Vision Research · doi:10.1016/j.visres.2009.03.019 · Cited by 132 · see citing works
Mulder, M. J., Bos, D., Weusten, J. M. H., van Belle, J., van Dijk, S. C., Simen, P., van Engeland, H., & Durston, S. (2010) · Biological Psychiatry · doi:10.1016/j.biopsych.2010.07.031 · Cited by 131 · see citing works
Mormann, M., Malmaud, J., Huth, A. G., Christof Koch, A., & Rangel, A. (2011) · SSRN Electronic Journal · doi:10.2139/ssrn.1901533 · Cited by 130 · see citing works
Kelly, S. P., & O’Connell, R. G. (2014) · Journal of Physiology-Paris · doi:10.1016/j.jphysparis.2014.08.003 · Cited by 128 · see citing works
Perceptual decisions are biased by the cost to act
Hagura, N., Haggard, P., & Diedrichsen, J. (2017) · eLife · doi:10.7554/elife.18422 · Cited by 126 · see citing works
Confidence Is the Bridge between Multi-stage Decisions
van den Berg, R., Zylberberg, A., Kiani, R., Shadlen, M. N., & Wolpert, D. M. (2016) · Current Biology · doi:10.1016/j.cub.2016.10.021 · Cited by 125 · see citing works
Self-citationSeparate, Causal Roles of the Caudate in Saccadic Choice and Execution in a Perceptual Decision Task
Ding, L., & Gold, J. I. (2012) · Neuron · doi:10.1016/j.neuron.2012.07.021 · Cited by 125 · see citing works
Unfalsifiability and mutual translatability of major modeling schemes for choice reaction time.
Jones, M., & Dzhafarov, E. N. (2013) · Psychological Review · doi:10.1037/a0034190 · Cited by 125 · see citing works
How does neuroscience affect our conception of volition?
Roskies, A. (2010) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-060909-153151 · Cited by 113 · see citing works
Global motion perception deficits in autism are reflected as early as primary visual cortex
Robertson, C. E., Thomas, C., Kravitz, D. J., Wallace, G. L., Baron-Cohen, S., Martin, A., & Baker, C. I. (2014) · Brain · doi:10.1093/brain/awu189 · Cited by 122 · see citing works
The Functional Anatomy of a Perceptual Decision in the Human Brain
Kayser, A. S., Buchsbaum, B. R., Erickson, D. T., & D’Esposito, M. (2009) · Journal of Neurophysiology · doi:10.1152/jn.00364.2009 · Cited by 118 · see citing works
Motor effort alters changes of mind in sensorimotor decision making
Burk, D., Ingram, J. N., Franklin, D. W., Shadlen, M. N., & Wolpert, D. M. (2014) · PLoS ONE · doi:10.1371/journal.pone.0092681 · Cited by 117 · see citing works
Self-citationTrial-by-trial fluctuations in CNV amplitude reflect anticipatory adjustment of response caution
Boehm, U., van Maanen, L., Forstmann, B. U., & van Rijn, H. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2014.03.063 · Cited by 117 · see citing works
Rapid decision threshold modulation by reward rate in a neural network
Simen, P., Cohen, J. D., & Holmes, P. J. (2006) · Neural Networks · doi:10.1016/j.neunet.2006.05.038 · Cited by 116 · see citing works
Modeling reaction time and accuracy of multiple-alternative decisions
Leite, F. P., & Ratcliff, R. (2009) · Attention Perception & Psychophysics · doi:10.3758/app.72.1.246 · Cited by 115 · see citing works
Loughnane, G. M., Newman, D. P., Bellgrove, M. A., Lalor, E. C., Kelly, S. P., & O’Connell, R. G. (2016) · Current Biology · doi:10.1016/j.cub.2015.12.049 · Cited by 113 · see citing works
How mechanisms of perceptual decision-making affect the psychometric function
Gold, J. I., & Ding, L. (2012) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2012.05.008 · Cited by 112 · see citing works
Representational geometry of perceptual decisions in the monkey parietal cortex
Okazawa, G., Hatch, C. E., Mancoo, A., Machens, C. K., & Kiani, R. (2021) · Cell · doi:10.1016/j.cell.2021.05.022 · Cited by 111 · see citing works
Zhang, J., & Rowe, J. B. (2014) · Frontiers in Neuroscience · doi:10.3389/fnins.2014.00069 · Cited by 110 · see citing works
Thura, D., Cos, I., Trung, J., & Cisek, P. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.0162-14.2014 · Cited by 109 · see citing works
Human Scalp Potentials Reflect a Mixture of Decision-Related Signals during Perceptual Choices
Philiastides, M. G., Heekeren, H. R., & Sajda, P. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.3012-14.2014 · Cited by 110 · see citing works
Models, movements, and minds: bridging the gap between decision making and action
Wispinski, N. J., Gallivan, J. P., & Chapman, C. S. (2018) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.13973 · Cited by 105 · see citing works
Models and processes of multisensory cue combination
Seilheimer, R. L., Rosenberg, A., & Angelaki, D. E. (2013) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2013.11.008 · Cited by 105 · see citing works
Shadmehr, R., & Ahmed, A. A. (2020) · The MIT Press eBooks · doi:10.7551/mitpress/12940.001.0001 · Cited by 103 · see citing works
FoxP influences the speed and accuracy of a perceptual decision in Drosophila
Dasgupta, S., Ferreira, C. H., & Miesenböck, G. (2014) · Science · doi:10.1126/science.1252114 · Cited by 102 · see citing works
Visual Decision-Making in an Uncertain and Dynamic World
Gold, J. I., & Stocker, A. A. (2017) · Annual Review of Vision Science · doi:10.1146/annurev-vision-111815-114511 · Cited by 100 · see citing works
Comparing fixed and collapsing boundary versions of the diffusion model
Voskuilen, C., Ratcliff, R., & Smith, P. L. (2016) · Journal of Mathematical Psychology · doi:10.1016/j.jmp.2016.04.008 · Cited by 100 · see citing works
- Authors
- Palmer, J., Huk, A. C., & Shadlen, M. N.
- Affiliations
- University of Washington (US)
- The University of Texas at Austin (US)
- Howard Hughes Medical Institute (US)
- Venue
- Journal of Vision
- Published
- 2005-05-02
- Volume
- 5
- Issue
- 5
- Pages
- 1
- ISSN
- 1534-7362 (ISSN-L)
- OpenAlex
- W2135075084
- Semantic Scholar
- abf73168fa849aa554fea630060ed3f593512493
- Cited by
- 691
- References
- 89
- Citations by year
- 2026: 17 · 2025: 36 · 2024: 29 · 2023: 38 · 2022: 47 · 2021: 43 · 2020: 36 · 2019: 25 · 2018: 39 · 2017: 27 · 2016: 39 · 2015: 47 · 2014: 51 · 2013: 39 · 2012: 35
- FWCI
- 11.07
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- Journal of Vision (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Eye Institute (EY11378, R01EY011378)
- National Center for Research Resources (RR00166, P51RR000166)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Visual perception and processing mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural and Behavioral Psychology Studies
- Social Sciences › Decision Sciences › General Decision Sciences › Decision-Making and Behavioral Economics
- Keywords
- perceptual decision making, stimulus strength, reaction time (psychology), decision accuracy, diffusion models, psychometric functions, speed-accuracy trade-off, sensory evidence accumulation
- MeSH terms
- Decision Making, Humans, Psychometrics, Psychomotor Performance, Reaction Time, Visual Perception, Reproducibility of Results
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review