Visual determinants of a cross-modal illusion

Contrary to the predictions of established theory, Schutz and Lipscomb (2007) have shown that visual information can influence the perceived duration of concurrent sounds. In the present study, we deconstruct the visual component of their illusion, showing that (1) cross-modal influence depends on visible cues signaling an impact event (namely, a sudden change of direction concurrent with tone onset) and (2) the illusion is controlled primarily by the duration of post-impact motion. Other aspects of the post-impact motion—distance traveled, velocity, acceleration, and the rate of its change (i.e., its derivative, jerk)—play a minor role, if any. Together, these results demonstrate that visual event duration can influence the perception of auditory event duration, but only when stimulus cues are sufficient to give rise to the perception of a causal cross-modal relationship. This refined understanding of the illusion’s visual aspects is helpful in comprehending why it contrasts so markedly with previous research on cross-modal integration, demonstrating that vision does not appreciably influence auditory judgments of event duration (Walker & Scott, 1981).     

The effect of timing and spatial separation on the velocity of auditory apparent motion

Previously, it was shown that the minimum conditions for the illusion of auditory apparent motion (AAM) depend on stimulus timing but not spatial separation. In the present experiment, the effects of stimulus timing and source separation on the perceived velocity of AAM were examined. Eight listeners estimated the velocity, duration, and distance traveled of AAM, using a no-modulus, magnitude estimation procedure. Four burst durations (25, 50, 100, and 300 msec), 10 stimulus onset asynchronies (SOAs; 30, 40, 50, 60, 70, 80, 90, 100, 110, and 120 msec) and two separations (10° and 40°) were tested. Perceived velocity estimates were related to the total duration (burst duration + SOA) of the stimulus sequence. The effect of separation on velocity was extremely small but statistically significant. These results are similar to those obtained previously on the minimum conditions for AAM. Duration estimates were related only to total duration, but separation estimates were related to both separation and total duration. These results suggest that velocity is possibly a primary dimension of AAM that is independent of source separation.     

Auditory apparent motion in the free field: The effects of stimulus duration and separation

The effects of stimulus duration and spatial separation on the illusion of apparent motion in the auditory modality were examined. Two narrow-band noise sources (40 dB, A-weighted) were presented through speakers separated in space by 2.5°, 5°, or 100, centered about the subject’s midline. The duration of each stimulus was 5, 10, or 50 msec. On each trial, the sound pair was temporally separated by 1 of 10 interstimulus onset intervals (ISOIs): 0, 2, 4, 6, 8, 10, 15, 20, 50, or 70 msec. Five subjects were tested in nine trial blocks; each block represented a particular spatial-separation-duration combination. Within a trial block, each ISOI was presented 30 times each, in random order. Subjects were instructed to listen to the stimulus sequence and classify their perception of the sound into one of five categories: single sound, simultaneous sounds, continuous motion, broken motion, or successive sounds. Each subject was also required to identify the location of the first-occurring stimulus (left or right). The percentage of continuous-motion responses was significantly affected by the ISOI [F(9,36) = 5.67,p < .001], the duration × ISOI interaction [F(18,72) = 3.54,p < .0001], and the separation × duration × ISOI interaction [F(36,144) = 1.51,p < .05]. The results indicate that a minimum duration is required for the perception of auditory apparent motion. Little or no motion was reported at durations of 10 msec or less. At a duration of 50 msec, motion was reported most often for ISOIs of 20–50 msec. The effect of separation appeared to be limited to durations and-ISOIs during which little motion was perceived.     

线索提示对表征动量的影响

研究结合线索提示和表征动量范式,实验1、2均采用2有无线索(有线索,无线索)×4诱导期间时距(1250ms,1750ms,2250ms,2750ms)混合实验设计,探讨线索呈现的加工阶段和时距对表征动量的影响。实验1恒定保持间隔时距,在不同时距的诱导期间呈现线索,发现线索主效应不显著,但表征动量呈减小趋势;时距主效应不显著。实验2变化诱导时距,在恒定的保持间隔呈现线索,发生向后偏移现象,线索主效应显著;时距主效应不显著。研究结果表明,随着注意的增加,表征动量效应减小;注意时距不显著影响表征动量,而注意阶段显著影响表征动量。研究结果为表征动量的双加工理论提供了实证支持。     

Joint control strategies and hand trajectories in multijoint pointing movements

The role of timing in the control of multijoint pointing movements was evaluated. Eight subjects performed rapid pointing movements to a variety of target locations. The subject's right arm was strapped to a 2 degrees of freedom manupilandum that permitted shoulder and elbow motion in the horizontal plane. Initial and final position of the hand and magnitude of displacement was varied to determine effects on timing characteristics. Kinematics and kinetics of the shoulder, elbow, and hand were analyzed. The hand paths and velocity profiles observed were consistent with prior reports. Multiple regression analysis of kinematic variables disclosed that timing of joint movement onset was independent of initial and final positions of the hand, but was linearly related to joint displacement: the joint that moved farther started moving first. Using computer simulations to create joint movement onset, times that were different from the observed ones always resulted in hand paths with increased curvatures and loss of the smooth velocity profiles. Secondly, a very stable, linear relationship was observed between peak velocity and displacement at both the elbow and shoulder joints. This relationship was not affected by variations in movement space. We suggest that space-time transformation based on difference in joint displacement is used to regulated timing of joint movement onset. The simulations indicate that this transformation is set to produce smooth velocity profiles. The relationships between timing of movement onset and displacement and between peak velocity and displacement complement each other: by maintaining a linear relationship between velocity and displacement, a linear space time transformation can be used to control timing. Furthermore, these relationships are probably used to simplify coordination between the moving joints.     

The effect of refractive error on central and peripheral motion sensitivity at various exposure durations

Pennsylvania State University, University Park, Pennsylvania 16802 The influence of refractive error on movement sensitivity was determined for a range of stimulus durations in the fovea and periphery. At short durations, threshold is determined by a constant displacement of the stimulus. At longer durations, a constant velocity is required. The correction of peripheral refractive error increases movement sensitivity in the displacement (short duration) component, but does not influence sensitivity in the velocity (long duration) component of the motion threshold. Implications concerning the mechanisms underlying motion perception are discussed.     

Relation Between EMG Activation Patterns and Kinematic Properties of Aimed Arm Movements

Aimed flexion movements of the arm of different amplitude and duration were studied. Velocity and acceleration traces of movements with equal duration but different amplitude were equal, apart from a scaling factor (ratio between movement amplitudes). After appropriate scaling, EMG activity of the first agonist burst for these movements superimposed. This was not true for EMG activity in the antagonist muscle.

For movements with equal amplitude, but different duration, the time to peak acceleration was constant for all MT’s. Except for this fact, traces of acceleration, velocity, and agonist activity following the time of peak acceleration were about equal after appropriate scaling in time and amplitude. The integral of EMG activity in the first agonist burst increased linearly with peak velocity. For the antagonist burst, the integrated EMG activity increased more than proportionally.

During movements made as fast as possible, subjects used a different strategy by varying the duration of the accelerating phase for movements of different amplitude. Movement amplitude was achieved by adjusting the duration of the agonist burst and the onset time for the antagonist muscle. Amplitude of the antagonist burst was constant within a narrow range for movements of different amplitude.

These results did not change when the inertial mass was doubled by loading the arm with an additional mass.     

Environmental invariants in the representation of motion: Implied dynamics and representational momentum,gravity, friction,and centripetal force

Memory for the final position of a moving target is often shifted or displaced from the true final position of that target. Early studies of this memory shift focused on parallels between the momentum of the target and the momentum of the representation of the target and called this displacementrepresentational momentum, but many factors other than momentum contribute to the memory shift. A consideration of the empirical literature on representational momentum and related types of displacement suggests there are at least four different types of factors influencing the direction and magnitude of such memory shifts: stimulus characteristics (e.g., target direction, target velocity), implied dynamics and environmental invariants (e.g., implied momentum, gravity, friction, centripetal force), memory averaging of target and nontarget context (e.g., biases toward previous target locations or nontarget context), and observers’ expectations (both tacit and conscious) regarding future target motion and target/context interactions. Several theories purporting to account for representational momentum and related types of displacement are also considered.     

Detection of changes in speed and direction of motion: Reaction time analysis

Observers reacted to the change in the movement of a random-dot field whose initial velocity,V _o, was constant for a random period and then switched abruptly to another value,V ₁. The two movements, both horizontally oriented, were either in the same direction (speed increments or decrements), or in the opposite direction but equal in speed (direction reversals). One of the two velocities,V ₀ orV ₁, could be zero (motion onset and offset, respectively). in the range of speeds used, 0–16 deg/sec (dps), the mean reaction time (MRT) for a given value ofV ₀ depended on |V ₁-V ₀| only: MRT ≈r +c(V ₀/|V ₁ ?V ₀|) ^β , where β=2/3,r is a velocity-independent component of MRT, andc(V ₀) is a parameter whose value is constant for low values ofV ₀ (0–4 dps), and increases beginning with some value ofV ₀ between 4 and 8 dps. These and other data reviewed in the paper are accounted for by a model in which the time-position function of a moving target is encoded by mass activation of a network of Reichardt-type encoders. Motion-onset detection (V ₀=0) is achieved by weighted temporal summation of the outputs of this network, the weights assigned to activated encoders being proportional to their squared spatial spans. By means of a “subtractive normalization,” the visual system effectively reduces the detection of velocity changes (a change fromV ₀ toV ₁) to the detection of motion onset (a change from 0 toV ₁-V ₀). Subtractive normalization operates by readjustment of weights: the weights of all encoders are amplified or attenuated depending on their spatial spans, temporal spans, and the initial velocityV ₀. Assignment of weights and weighted temporal summation are thought of as special-purpose computations performed on the dynamic array of activations in the motion-encoding network, without affecting the activations themselves.     

Detectability of duration and intensity increments in melody tones: A partial connection between music perception and performance

Two experiments demonstrate positional variation in the relative detectability of, respectively, local temporal and dynamic perturbations in an isochronous and isodynamic sequence of melody tones, played on a computer-controlled piano. This variation may reflect listeners’ expectations of expressive performance microstructure (thetop-down hypothesis), or it may be due to psychoacoustic (pitch-related) stimulus factors (thebottom-up hypothesis). Percent correct scores for increments in tone duration correlated significantly with the average timing profile of pianists’ expressive performances of the music, as predicted specifically by the top-down hypothesis. For intensity increments, the analogous perception-performance correlation was weak and the bottom-up factors of relative pitch height and/or direction of pitch change accounted for some of the perceptual variation. Subjects’ musical training increased overall detection accuracy but did not affect the positional variation in accuracy scores in either experiment. These results are consistent with the top-down hypothesis for timing, but they favor the bottom-up hypothesis for dynamics. The perception-performance correlation for timing may also be viewed as being due to complex stimulus properties such as tonal motion and tension/relaxation that influence performers and listeners in similar ways.     

Observations on stroboscopic induced motion

Subject-relative explanations of motion induction state that induced motion is the result of a misperceived shift of the median plane of the visual field of the subject. This theory does not require relative motion of the spot and frame, in the classical spot-and-frame condition, only asymmetrical stimulation. Three experiments are reported in which stroboscopic induced motion was investigated. The experimental arrangement was unconventional in that the induced object (spot) was presented only during the interstimulus interval between the exposures of the inducing object (frame). This allowed differentiation of the duration of the induced movement and that of the inducing one. In the first experiment it was demonstrated that perception of induced motion depends upon the duration of the interstimulus interval between the presentations of the inducing frame. In the second experiment it was shown that the perceived velocity of the induced movement can be different from that of the inducing one and depends on the duration of exposure of the induced object. In the third experiment a stimulus display was created in which the apparent displacement of an object and its induced motion are incongruous. The results are incompatible with subject-relative displacement as the sole determining factor of motion induction and they present some difficulties for the hypothesis that induced motion is the result of the apportionment of the objective displacement of the frame.     

Real-time manipulation of visual displacement during manual aiming

This study examined the spatial and temporal limitations of the visual corrective process in the control of upper limb movements. Real-time calculation of kinematic data was used to trigger a prismatic displacement of the movement environment during manual aiming. Using an OptoTrak motion tracking system, a data acquisition unit, and a custom-made program, perturbations were triggered at peak acceleration, peak velocity, and the estimated time of peak deceleration. Movement outcome was significantly influenced only when the visual displacement occurred at peak acceleration. The results support models of visual control that posit that early visual information is required for accurate limb control.     

Amplitude rise time and the perception of the voiceless affricate/fricative distinction

Variation of amplitude envelope at stimulus onset has been considered to be of primary importance for distinguishing voiceless affricates from fricatives (e.g., |t∫| and |∫|). In earlier perceptual experiments, however, variation in amplitude rise time was confounded with variation in frication duration. In two experiments, these variables were independently manipulated, and their individual and combined effects for perception of |t∫| and |∫| were examined. Variation in amplitude rise time alone was not sufficient to signal the voiceless affricate/fricative contrast in these experiments, but variation in frication duration alone was sufficient.     

Providing a sensory basis for models of visual information acquisition

Our major goal is to account for some simple digit-recall data with a theory that integrates two models from two scientific traditions. Therandom-sampling model, founded in the memory and attention literature, holds that (1) stimulus features are randomly sampled throughout the course of stimulus presence and (2) proportion correct recall is equal to the ratio of sampled features to total features.The linear-filter model, founded in the vision and sensation literature, holds that the initial stages of the visual system act as a low-pass temporal filter on the input stimulus, resulting in a time-varyingsensory response in the nervous system. We report two experiments in which a variable-duration, masked, four-digit string had to be immediately recalled. Experiment 1 was designed principally to replicate past data confirming the basic random-sampling model. Like others, we were able to confirm the model only by endowing it with an additionalprocessing-delay assumption: that feature sampling does not begin until the stimulus has been physically present for some minimal duration. Experiment 2 was an extension of Experiment 1 in which the target stimulus was preceded, 250 msec prior to its onset, by a 50-msec pre-presentation ofthe same stimulus called aprime. The Experiment 2 results allowed the following conclusions. First, the initial processing delay found in Experiment 1 is immutably tied to stimulus onset; that is, if there are two stimulus onsets, separated even briefly in time, there are two associated processing delays. Second, processing rate is essentially unaffected by the prime’s presentation. Third, being presented with a 50-msec prime is equivalent, in terms of memory performance, to increasing unprimed stimulus duration by approximately 30 msec; the prime can thus said to beworth 30 msec of additional exposure duration. This third conclusion seems superficially paradoxical, in the sense that one would expect that having seen a 50-msec prime would be equivalent to increasing exposure duration byat least the same 50 msec. However, both the initial processing delays and the 30-msec prime’s worth are natural consequences of our theory that conjoins the random-sampling model with the linear-filter model.     

What determines the detection of changes in motion velocity? A comment on Dzhafarov,Sekuler, and Allik (1993)

We comment on a recent model aimed at explaining data on speed of reaction to motion onset and to changes in motion velocity. The model is based on calculating the running variance of the stimulus positions passed during the motion. We show that although the model is successful in explaining data on motion onset and suprathreshold velocity changes, it may not be able to explain data on time of reaction to changes in velocity when these are near the detection threshold.     

速度知识和表征动量

通过3个实验探索速度知识和表征动量的关系。3个实验均使用2（速度知识：快、慢）×2（运动方向：左、右）的两因素实验设计,采用诱导运动范式,因变量为偏移加权均数。实验1使用汽车和自行车作为刺激材料,发现两者的前移量无差异;实验2使用人奔跑和站立姿势作为刺激材料,发现奔跑的前移量大于站立的前移量;实验3是控制实验,发现实验2的结果不是由水平视角差异造成的。结论：在有效启动速度概念的情况下,速度知识可以影响表征动量,但其影响可能相对微弱。     

The Conjunction Effect: Fallacy or Bayesian Inference?

It has been suggested by Wolford, Taylor, and Beck (1990) that the conjunction fallacy is not really a fallacy at all but arises when individuals misconstrue the judgmental problem providing estimates of the kind P(X|A&B) or P(X|B) (reverse probabilities) instead of the actual quantities that are being sought by the experimenter: P(A&B|X) or P(B|X). As pointed out by Wolford and co-workers, while the following judgment, P(A&B|X) > P(B|X), is a violation of the conjunction rule, outcomes such as P(X|A&B) > P(X|B) do not necessarily violate any probabilistic law. In an attempt to de-bias the judgment process, in Study 1 participants were requested to provide both types of probabilities at the same time. The results revealed a drop in the incidence of the conjunction fallacy to 32% averaged over all scenarios compared with 57% for the same scenarios in an earlier study. In each scenario the two sets of estimates, normal and reverse, were significantly different from each other indicating that participants were capable of distinguishing between the two concepts. Despite this fact in two of the four scenarios a significant minority of participants (44 and 49%) continued to commit the fallacy. These combined outcomes cast doubt on Wolfordet al.’s (1990) account of the fallacy. In addition, Studies 2 and 3 showed that under certain conditions, most participants’ judgments of the kind P(X|A&B) > P(X|B), far from being normative, were inconsistent with Bayes’ theorem even in broad terms.     

Comparing Three New MMPI-2 Randomness Indices in a Novel Procedure for Random Profile Derivation

This study compared three new validity indices; |F-Fb|, VRIN+|F-Fb|, and F+Fb+|F-Fb|; to the F, back-F, and VRIN according to their effectiveness in detecting degrees of profile randomness. Participants completed the Minnesota Multiphasic Personality Inventory-2 (MMPI-2; Butcher, Dahlstrom, Graham, Tellegen, and Kaemmer, 1989) according to standardized instructions. All profiles starting at Items 142, 284, or 426 were substituted with computer-generated random responses to produce 75%, 50%, and 25% random profiles, respectively. Twenty-five profiles were derived using 100% computer-generated items. Finally, one unaltered set of profiles was designated as 0% random. This generated five groups of MMPI-2 profiles, differing according to the degree of profile randomness (i.e., 0%, 25%, 50%, 75%, and 100%). Results showed that the F and |F-Fb| indices were unable to distinguish authentic from all degrees of randomness, whereas the F+Fb+F-Fb scale could reliably distinguish all levels of randomness. The actuarial analysis found back-F and F+Fb+|F-Fb| misclassified the least number of profiles, suggesting the latter index should be included in the evaluation of MMPI-2 profile randomness.     

Visual onset expands subjective time

We report a distortion of subjective time perception in which the duration of a first interval is perceived to be longer than the succeeding interval of the same duration. The amount of time expansion depends on the onset type defining the first interval. When a stimulus appears abruptly, its duration is perceived to be longer than when it appears following a stationary array. The difference in the processing time for the stimulus onset and motion onset, measured as reaction times, agrees with the difference in time expansion. Our results suggest that initial transient responses for a visual onset serve as a temporal marker for time estimation, and a systematic change in the processing time for onsets affects perceived time.