nips nips2001 nips2001-11 knowledge-graph by maker-knowledge-mining
Source: pdf
Author: H. Colonius, A. Diederich
Abstract: Multisensory response enhancement (MRE) is the augmentation of the response of a neuron to sensory input of one modality by simultaneous input from another modality. The maximum likelihood (ML) model presented here modifies the Bayesian model for MRE (Anastasio et al.) by incorporating a decision strategy to maximize the number of correct decisions. Thus the ML model can also deal with the important tasks of stimulus discrimination and identification in the presence of incongruent visual and auditory cues. It accounts for the inverse effectiveness observed in neurophysiological recording data, and it predicts a functional relation between uni- and bimodal levels of discriminability that is testable both in neurophysiological and behavioral experiments. 1
Reference: text
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1 de Abstract Multisensory response enhancement (MRE) is the augmentation of the response of a neuron to sensory input of one modality by simultaneous input from another modality. [sent-5, score-0.795]
2 The maximum likelihood (ML) model presented here modifies the Bayesian model for MRE (Anastasio et al. [sent-6, score-0.087]
3 ) by incorporating a decision strategy to maximize the number of correct decisions. [sent-7, score-0.028]
4 Thus the ML model can also deal with the important tasks of stimulus discrimination and identification in the presence of incongruent visual and auditory cues. [sent-8, score-0.394]
5 It accounts for the inverse effectiveness observed in neurophysiological recording data, and it predicts a functional relation between uni- and bimodal levels of discriminability that is testable both in neurophysiological and behavioral experiments. [sent-9, score-0.609]
6 1 Introduction In a typical environment stimuli occur at various positions in space and time. [sent-10, score-0.16]
7 In order to produce a coherent assessment of the external world an individual must constantly discriminate between signals relevant for action planning (targets) and signals that need no immediate response (distractors). [sent-11, score-0.236]
8 Separate sensory channels process stimuli by modality, but an individual must determine which stimuli are related to one another, i. [sent-12, score-0.385]
9 For example, stimuli that occur at the same time and space are likely to be interrelated by a common cause. [sent-15, score-0.136]
10 However, if the visual and auditory cues are incongruent, e. [sent-16, score-0.237]
11 , when dubbing one syllable onto a movie showing a person mouthing a different syllable, listeners typically report hearing a third syllable that represents a combination of what was seen and heard (McGurk effect, cf. [sent-18, score-0.156]
12 This indicates that cross-modal synthesis is particularly important for stimulus identification and discrimination, not only for detection. [sent-20, score-0.094]
13 Evidence for multisensory integration at the neural level has been well documented in a series of studies in the mammalian midbrain by Stein, Meredith and Wallace (e. [sent-21, score-0.639]
14 The deep layers of the superior colliculus (DSC) â€Ë˜ www. [sent-24, score-0.082]
15 html integrate multisensory input and trigger orienting responses toward salient targets. [sent-28, score-0.685]
16 Multisensory response enhancement refers to the augmentation of the response of a DSC neuron to a multisensory stimulus compared to the response elicited by the most effective single modality stimulus. [sent-30, score-1.386]
17 A quantitative measure of the percent enhancement is MRE = CM - SMmax x 100, SMmax (1) where CM is the mean number of impulses evoked by the combined-modality stimulus in a given time interval, and S Mmax refers to the response of the most effective single-modality stimulus (cf. [sent-31, score-0.592]
18 Response enhancement in the DSC neurons can be quite impressive, with values of M RE sometimes reaching values above 1000. [sent-33, score-0.327]
19 Typically, this enhancement is most dramatic when the unimodal stimuli are weak and/or ambiguous, a principle referred to in [4] as "inverse effectiveness" . [sent-34, score-0.596]
20 Inverse effectiveness makes intuitive sense in the behavioral situation: the detection probability for a weak or ambiguous stimulus gains more from response enhancement by multisensory integration than a highintensity stimulus that is easily detected by a single modality alone. [sent-38, score-1.398]
21 A model of the functional significance of multisensory enhancement has recently been proposed by Anastasio, Patton, and Belkacem-Boussaid [9]. [sent-39, score-0.855]
22 They suggested that the responses of individual DSC neurons are proportional to the Bayesian probability that a target is present given their sensory inputs. [sent-40, score-0.325]
23 Here, this Bayesian model is extended to yield a more complete account of the decision situation an organism is faced with. [sent-41, score-0.157]
24 As noted above, in a natural environment an individual is confronted with the task of discriminating between stimuli important for survival (" targets") and stimuli that are irrelevant (" distractors") . [sent-42, score-0.361]
25 Thus, an organism must not only keep up a high rate of detecting targets but, at the same time, must strive to minimize " false alarms" to irrelevant stimuli. [sent-43, score-0.163]
26 It will be shown here that this can be achieved already at the level of individual DSC neurons by appealing to a maximum-likelihood principle, without requiring any more information than is assumed in the Bayesian model. [sent-45, score-0.125]
27 The next section sketches the Bayesian model by Anastasio, Patton, and BelkacemBoussaid (Bayesian model, for short), after which a maximum-likelihood model of multisensory response enhancement will be introduced. [sent-46, score-0.966]
28 2 The Bayesian Model of Multisensory Enhancement DSC neurons receive input from the visual and auditory systems elicited by stimuli occurring within their receptive fields! [sent-47, score-0.564]
29 According to the Bayesian model, these vii An extension to the trimodal situation, including somatosensory input, could be easily attained in the models discussed here. [sent-48, score-0.065]
30 sual and auditory inputs are represented by random variables V and A, respectively. [sent-49, score-0.203]
31 The response of the DSC neuron (number of spikes in a unit time interval) is postulated to be proportional to these probabilities. [sent-53, score-0.189]
32 In order to arrive at quantitative predictions two more specific assumptions are made: (1) the distributions of V and A, given T = 1 or T = 0, are conditionally independent , i. [sent-54, score-0.039]
33 The conditional independence assumption means that the visibility of a target indicates nothing about its audibility, and vice-versa. [sent-58, score-0.082]
34 Finally, the computation of the posterior probability that a target is present requires specification of the a-priori probability of a target, P(T = 1). [sent-60, score-0.082]
35 The parameters Ao and {-to denote the mean intensity of the visual and auditory input, resp. [sent-61, score-0.293]
36 , when no target is present (spontaneous input) , while Al and {-tl are the corresponding mean intensities when a target is present (driven input). [sent-62, score-0.164]
37 [9] show that the Bayesian model reproduces values of multisensory response enhancement in the order of magnitude observed in neurophysiological experiments [10]. [sent-64, score-1.005]
38 In particular, the property of inverse effectiveness, by which the enhancement is largest for combined stimuli that evoke only small unimodal responses , is reflected by the model. [sent-65, score-0.668]
39 1 The Maximum Likelihood Model of Multisensory Enhancement The decision rule The maximum likelihood model (ML model, for short) incorporates the basic decision problem an organism is faced with in a typical environment: to discriminate between relevant stimuli (targets), i. [sent-67, score-0.447]
40 , signals that require immediate reaction, and irrelevant stimuli (distractors), i. [sent-69, score-0.192]
41 , signals that can be ignored in a given situation. [sent-71, score-0.026]
42 [11]) , P(Yes IT = 1) denotes the probability that the organism (correctly) decides that a target is present (hit), while P(Yes IT = 0) denotes the probability of deciding that a target is present when in fact only a distractor is present (false alarm). [sent-73, score-0.246]
43 In order to maximize the probability of a correct response, P(C) = P(Yes IT = 1) P(T = 1) + [1- P(Yes IT = O)]P(T = 0), (3) the following maximum likelihood decision rule must be adopted (cf. [sent-74, score-0.094]
44 , the unimodal visual case: If P(T = 11 V = v) > P(T = 0 IV = v), then decide "Yes", otherwise decide " No" . [sent-77, score-0.395]
45 The above inequality is equivalent to P(T=IIV=v) P(T = 0 IV = v) P(T=I)P(v=vIT=I) P(T = 0) P(V = v IT = 0) > 1, where the right-most ratio is a function of V , L(V), the likelihood ratio. [sent-78, score-0.043]
46 Thus, the above rule is equivalent to: If L(v) > 1 - P , then decide "Yes" , otherwise decide "No" , P with p = P(T = 1). [sent-79, score-0.157]
47 Since L(V) is a random variable, the probability to decide "Yes" , given a target is present, is P (Yes I T = 1) = P (L(V) > 1; PIT = 1) . [sent-80, score-0.149]
48 2 Predictions for Hit Probabilities In order to compare the predictions of the ML model for unimodal vs. [sent-83, score-0.239]
49 990 13 3 Note: A-priori target probability is set at p = O. [sent-112, score-0.082]
50 Visual and auditory inputs have spontaneous means of 5 impulses per unit time. [sent-114, score-0.342]
51 V Driven (A Driven, V A Driven) columns refer to the hit probabilities given a unimodal visual (resp. [sent-115, score-0.452]
52 Multisensory response enhancement (last column) is computed using Eq. [sent-117, score-0.348]
53 Otherwise, hit probabilities follow the distribution of a linear combination of two Poisson distributed variables. [sent-122, score-0.191]
54 Table 1 presents 2 hit probabilities and multisensory response enhancement values for different levels of mean driven input. [sent-123, score-1.222]
55 Obviously, the ML model imitates the inverse effectiveness relation: combining weak intensity unimodal stimuli leads to a much larger response enhancement than medium or high intensity stimuli. [sent-124, score-0.964]
56 3 Predictions for discriminability measures The ML model allows to assess the sensitivity of an individual DSC neuron to discriminate between target and distract or signals. [sent-126, score-0.449]
57 Intuit ively, this sensitivity should be a (decreasing) function of the amount of overlap between the driven and the spontaneous likelihood (e. [sent-127, score-0.246]
58 One possible appropriate measure of sensitivity for the Poisson observer is (cf. [sent-130, score-0.037]
59 LO)l /4 (4) for the visual and auditory unimodal inputs, resp. [sent-135, score-0.415]
60 A natural choice for the bimodal measure of sensitivity then is D (AI + J. [sent-136, score-0.188]
61 (5) Note that, unlike the hit probabilities, the relative increase in discriminability by combining two unimodal inputs does not decrease with the intensity of the driven input (see Table 2). [sent-141, score-0.711]
62 Rather, the relation between bimodal and unimodal discriminability measures for the input values in Table 2 is approximately of Euclidean 2For input combinations with >'1 =I- J. [sent-142, score-0.552]
63 t1 hit probabilities are estimated from samples of 1,000 pseudo-random numbers. [sent-143, score-0.191]
64 Table 2: Discriminability measure values and % increase for different bimodal inputs Mean Driven Input Discriminability Value Al J. [sent-144, score-0.2]
65 97 41 41 26 Note: Visual and auditory inputs have spontaneous means of 5 impulses per unit time. [sent-163, score-0.342]
66 % Increase of Dv A over Dv and DA (last column) is computed in analogy to Eq. [sent-164, score-0.022]
67 The fact that the effectiveness rule should not hard to discriminate depends intensity. [sent-167, score-0.145]
68 Obviously, no claim is made here that the neuron actually performs these computations, only that its behavior can be described approximately in this way. [sent-169, score-0.076]
69 Similar to the Bayesian model suggested by Anastasio et al. [sent-170, score-0.022]
70 [9], the neuron's behavior is solely based on the a-priori probability of a target and the likelihood function for the different sensory inputs. [sent-171, score-0.203]
71 The ML model predicts the inverse effectiveness observed in neurophysiological experiments. [sent-172, score-0.202]
72 Moreover, the model allows to derive a measure of the neuron's ability to discriminate between targets and non-targets. [sent-173, score-0.133]
73 It makes specific predictions how un i- and bimodal discriminability measures are related and, thereby, opens up further avenues for testing the model assumptions . [sent-174, score-0.349]
74 The ML model, like the Bayesian model, operates at the level of a single DSC neuron. [sent-175, score-0.022]
75 However, an extension of the model to describe multisensory population responses is desirable: First, this would allow to relate the model predictions to numerous behavioral studies about multisensory effects (e. [sent-176, score-1.35]
76 [1 5) suggests, the effects of multisensory spatial coincidence observed in behavioral experiments may only be reconcilable with the degree of spatial resolution achievable by a population of DSC neurons with overlapping receptive fields. [sent-179, score-0.838]
77 Moreover, this extension might also be useful to relate behavioral and single-unit recording results to recent findings on multisensory brain areas using functional imaging techniques (e. [sent-180, score-0.677]
78 Converging influences from visual, auditory, and somatosensory cortices onto output neurons of the superior colliculus. [sent-196, score-0.179]
79 Spatial factors determine the activity of multisensory neurons in cat superior colliculus. [sent-210, score-0.688]
80 Spatial and temporal factors determine auditory-visual interactions in human saccadic eye movements. [sent-213, score-0.09]
81 A two stage-model for visual-auditory interaction in saccadic latencies. [sent-219, score-0.049]
82 Behavioral indices of multisensory integration: Orientation to visual cues is affected by auditory stimuli. [sent-229, score-0.811]
83 ), Handbook of perception and human performance, Volum e I : Sensory process and perception (pp . [sent-242, score-0.082]
84 Using Bayes' rule to model multisensory enhancement in the superior colliculus. [sent-248, score-0.924]
85 Visual, auditory, and somatosensory convergence on cells in superior colliculus results in multisensory integration. [sent-255, score-0.721]
86 Combining evidence presented simultaneously to the eye and the ear: A comparison of some predictive models. [sent-275, score-0.041]
87 Enhancement of perceived visual intensity by auditory stimuli: A psychophysical analysis. [sent-284, score-0.293]
88 The influence of visual and auditory receptive field organization on multisensory integration in the superior colliculus. [sent-295, score-0.953]
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For example, when X’s are frequent but Y is presented, individuals are predisposed toward producing the X response, and this predisposition must be overcome by the perceptual evidence from the Y. Jones and Braver (2001) also performed an fMRI study of this task and found that anterior cingulate cortex (ACC) becomes activated in situations involving response conflict. Specifically, when one stimulus occurs infrequently relative to the other, event-related fMRI response in the ACC is greater for the low frequency stimulus. Jones and Braver also extended a neural network model of Botvinick, Braver, Barch, Carter, and Cohen (2001) to account for human performance in the two discrimination tasks. The heart of the model is a mechanism that monitors conflict—the posited role of the ACC—and adjusts response biases accordingly. In this paper, we develop a parsimonious alternative account of the role of the ACC and of how control processes modulate behavior when response conflict arises. 1 A RATIONAL ANALYSIS Our account is based on a rational analysis of human cognition, which views cognitive processes as being optimized with respect to certain task-related goals, and being adaptive to the structure of the environment (Anderson, 1990). We make three assumptions of rationality: (1) perceptual inference is optimal but is subject to rate limitations on information transmission, (2) response class prior probabilities are accurately estimated, and (3) the goal of individuals is to minimize a cost that depends both on error rate and reaction time. The heart of our account is an existing probabilistic model that explains a variety of facilitation effects that arise from long-term repetition priming (Colagrosso, in preparation; Mozer, Colagrosso, & Huber, 2000), and more broadly, that addresses changes in the nature of information transmission in neocortex due to experience. We give a brief overview of this model; the details are not essential for the present work. The model posits that neocortex can be characterized by a collection of informationprocessing pathways, and any act of cognition involves coordination among pathways. To model a simple discrimination task, we might suppose a perceptual pathway to map the visual input to a semantic representation, and a response pathway to map the semantic representation to a response. The choice and go/no-go tasks described earlier share a perceptual pathway, but require different response pathways. The model is framed in terms of probability theory: pathway inputs and outputs are random variables and microinference in a pathway is carried out by Bayesian belief revision. To elaborate, consider a pathway whose input at time is a discrete random variable, denoted , which can assume values corresponding to alternative input states. Similarly, the output of the pathway at time is a discrete random variable, denoted , which can assume values . For example, the input to the perceptual pathway in the discrimination task is one of visual patterns corresponding to the letters of the alphabet, and the output is one of letter identities. (This model is highly abstract: the visual patterns are enumerated, but the actual pixel patterns are not explicitly represented in the model. Nonetheless, the similarity structure among inputs can be captured, but we skip a discussion of this issue because it is irrelevant for the current work.) To present a particular input alternative, , to the model for time steps, we clamp for . The model computes a probability distribution over given , i.e., P . ¡ # 4 0 ©2' & 0 ' ! 1)(
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