Variability and sequential effects in cross-modality matching of area and loudness

Individual subjects' performance was examined for cross-modality matching (CMM) of loudness to visual area, as well as for magnitude estimation (ME) of the component continua. Average exponents of power functions relating response magnitude to stimulus intensity were .73 for area, .20 for loudness, and 2.44 for CMM. Predictions of the CMM exponent based on ME were higher than the empirical values, whereas more accurate predictions were made from magnitude production exponents obtained in a previous study. Sequential dependencies were assessed by comparing the response on trial n to the response on trial n--1. The coefficient of variation of the response ratio Rn/Rn-1 was systematically related to the stimulus ratio Sn/Sn-1 for both area and loudness. The coefficient was lowest for ratios near 1 and increased for larger or smaller values. For CMM, the coefficient of variation appeared to be independent of stimulus ratios. The correlation between log Rn and log Rn-1 was also related to Sn/Sn-1 for both ME and CMM. The correlation was highest when Sn/Sn-1 was 1 and dropped to 0 with increasing stimulus separation, but CMM yielded a shallower function than ME.     

Response coding in the Simon task

Recent findings indicate that two distinct mechanisms can contribute to a Simon effect: a visuomotor information transmission on the one hand and a cognitive code interference on the other hand (see for e.g., Wiegand & Wascher, in Journal of Experimental Psychology: Human Perception and Performance 2005a). Furthermore, it was proposed that the occurrence of one or the other mechanism strongly depends on the way responses are coded. Visuomotor information transmission seems to depend on a correspondence between stimulus position and spatial anatomical status of the effector, whereas cognitive code interference is thought to be based on relative response location codes. To further test the spatial anatomic coding hypothesis, three experiments were conducted, in which the Simon effect with unimanual responses was investigated for horizontal (Experiment 1 and 2) and vertical (Experiment 3) stimulus-response (S-R) relations. Based on the finding of a decreasing effect function (indicating the presence of visuomotor information transmission) for horizontal and vertical S-R relations, it was concluded that visuomotor information transmission occurs whenever there is an overlap between the spatial stimulus feature and parameters of the motor representation of the response. Furthermore, the specific motor representation seems to be task dependent, that is, it entails those response parameters that clearly differentiate between the two response alternatives in a given task situation.     

Heart-rate and electrodermal orienting responses to visual stimuli differing in complexity

Orienting response (OR) theory predicts that amount of information in the stimulus, or stimulus complexity, should be an important determinant of OR elicitation and habituation, more intense and more slowly habituating ORs being expected to complex than to simple stimuli. This prediction was tested in an experiment where subjects were exposed to simple and complex visual stimuli in randomized order, while heart-rate and skin conductance were measured. Complex stimuli evoked a more pronounced deceleratory heartrate response than did simple stimuli. However, the two conditions did not differ in rate of habituation of this response. For skin conductance responses, on the other hand, the complex stimulus took more trials than the simple stimulus to reach habituation, whereas the two conditions did not differ in response magnitude. Thus, the hypothesis of more intense orienting to complex stimuli was supported by the heart-rate data, and that of slower habituation to complex stimuli, of the skin conductance data.     

Mixed-modality psychophysical scaling: Sequential dependencies and other properties

J. C. Stevens and Marks’s (1980) method of magnitude matching and a derivative, category matching, are examined in two experiments. Category matching produces highly similar matching functions to those of magnitude matching. The two methods are both subject to significant sequential dependencies, which, however, should not affect exponents of matching functions. Such mixed-modality scaling methods are also useful for theory testing. In the present case, responses were assimilated to the immediately previous response (different modality stimulus) but contrasted with the stimulus (same modality) two trials back in the sequence. The dependency of the response-response dependency on Sn-S_n-k was independent of stimulus modality. However, the usual dependency of the coefficient of variation of ratios of successive responses on Sn-S_n-k was not found. These results support the class of theories in which assimilative response-response dependencies and contrastive response-stimulus dependencies arise from different mechanisms, and disconfirm those in which both effects arise in a linked fashion from a single mechanism.     

Human observing: maintained by negative informative stimuli only if correlated with improvement in response efficiency.

Two experiments investigated the effect of observing responses that enabled college students to emit more efficient distributions of reinforced responses. In Experiment 1, the gains of response efficiency enabled by observing were minimized through use of identical low-effort response requirements in two alternating variable-interval schedules. These comprised a mixed schedule of reinforcement; they differed in the number of money-backed points per reinforcer. In each of three choices between two stimuli that varied in their correlation with the variable-interval schedules, the results showed that subjects preferred stimuli that were correlated with the larger average amount of reinforcement. This is consistent with a conditioned-reinforcement hypothesis. Negative informative stimuli--that is, stimuli correlated with the smaller of two rewards--did not maintain as much observing as stimuli that were uncorrelated with amount of reward. In Experiment 2, savings in effort made possible by producing S- were varied within subjects by alternately removing and reinstating the response-reinforcement contingency in a mixed variable-interval/extinction schedule of reinforcement. Preference for an uncorrelated stimulus compared to a negative informative stimulus (S-) decreased for each of six subjects, and usually reversed when observing permitted a more efficient temporal distribution of the responses required for reinforcement; in this case, the responses were pulls on a relatively high-effort plunger. When observing the S- could not improve response efficiency, subjects again chose the control stimulus. All of these results were inconsistent with the uncertainty-reduction hypothesis.     

Response competition: a major source of interference in a tactile identification task.

Two experiments investigated the ability of subjects to identify a moving, tactile stimulus. In both experiments, the subjects were presented with a target to their left index fingerpad and a nontarget (also moving) to their left middle fingerpad. Subjects were instructed to attend only to the target location and to respond "1" if the stimulus moved either to the left or up the finger, and to respond "2" if the stimulus moved either right or down the finger. The results showed that accuracy was better and reaction times were faster when the target and nontarget moved in the same direction than when they moved in different directions. When the target and nontarget moved in different directions, accuracy was significantly better and reaction times were significantly faster when the two stimuli had the same assigned response than when they had different responses. The results provide support for the conclusion that movement information is processed across adjacent fingers to the level of incipient response activation, even when subjects attempt to focus their attention on one location on the skin.     

Response competition: A major source of interference in a tactile identification task

Two experiments investigated the ability of subjects to identify a moving, tactile stimulus. In both experiments, the subjects were presented with a target to their left index fingerpad and a nontarget (also moving) to their left middle fingerpad. Subjects were instructed to attend only to the target location and to respond “1” if the stimulus moved either to the left or up the finger, and to respond “2” if the stimulus moved either right or down the finger. The results showed that accuracy was better and reaction times were faster when the target and nontarget moved in the same direction than when they moved in different directions. When the target and nontarget moved in different directions, accuracy was significantly better and reaction times were significantly faster when the two stimuli had the same assigned response than when they had different responses. The results provide support for the conclusion that movement information is processed across adjacent fingers to the level of incipient response activation, even when subjects attempt to focus their attention on one location on the skin.     

The effects of a pre-time-out stimulus on matching-to-sample of humans,

In each of two experiments human subjects were intermittently reinforced with money on a fixed-ratio schedule for emitting correct matching responses. A pre-time-out stimulus which signaled removal of positive reinforcement was periodically superimposed. In the first experiment the superimposed pre-time-out stimulus was paired with a 1-min or 4-min response-independent time out. In the second experiment the pre-time-out stimulus was paired with a 1-min or 4-min time out contingent on the incorrect responses. The pre-time-out stimulus did not markedly influence performance when the time out was response independent. In contrast, the pre-time-out stimulus markedly suppressed incorrect responding when the time out was contingent on the incorrect responses. When duration of this time-out was increased from 1-min to 4-min, suppression of incorrect responding increased and correct responding was suppressed. Therefore, behavioral suppression by a pre-time-out stimulus was obtained only when the signaled aversive event-time out-was response produced. In this case, suppression was influenced by time-out duration.     

Range effects of an irrelevant dimension on classification

In univariate classification tasks, subjects sort stimuli on the basis of the only attribute that varies. In orthogonal classification tasks, often called filtering tasks, there additionally are trial-to-trial variations in irrelevant attributes that the subjects are instructed to ignore. Performance is generally slower in filtering tasks than in univariate control tasks. We investigated this slowing in experiments of how the range of irrelevant trial-to-trial variation affects responses in pitch/loudness classification tasks. Using two levels of pitch and of loudness as stimuli, Experiment 1 replicated prior work showing that responses are slowed more when the range of the irrelevant dimension is made larger. Also in Experiment 1, sequential analyses showed that response time depends both on sequence and on the stimulus set independent of sequence. Experiments 2 and 3 used several levels on the irrelevant dimension and showed that responses to categorize loudness are slowed more by larger trial-to-trial pitch differences, but only on trials when the response repeats. When the response changes, performance is essentially unaffected by trial-to-trial irrelevant variation. This interaction supports the conclusion that slowed average performance in orthogonal classification tasks, which is known as Garner interference, is not due to difficulties that subjects have in filtering stimulus attributes. It is due to how subjects process successive stimulus differences. We call for more frequent reports of sequential analyses, because these can reveal information that is not available from data averages.     

Risky decision: Attention and path dependency as a function of response mode

It was previously shown and was here replicated that the amount of money required to induce a subject to exchange one gamble for a second and then the second for a third depends on the second (intermediate) gamble. This path dependency cannot be explained by any of the algebraic models (including SEU), nor can it be explained as a simple attention effect. A model was put forward which explains the effect in terms of differential masking depending on a kind of stimulus—response compatibility. The effect of response mode on path dependency was examined in this study; similarity judgements showed no consistent path dependency nor did difference in rated attractiveness of gambles presented in pairs, but rated attractiveness was different for gambles presented singly. Since it might be that monetary response emphasises the monetary aspects, that is, the winning amount of the gamble, it was thought that a probability response would emphasise the probability of winning. However, when subjects were asked to set the probability of winning $ 12 which would induce them to exchange one gamble for another, not only was no path dependency observed, but the subjects' responses seemed to depend only on the difference in expected value of the gambles. This suggests the possibility of developing response-display modes which would eliminate or at least attenuate the inconsistencies observed in risky decision processes.     

Pre- and poststimulus activation of response channels: a psychophysiological analysis

To examine mechanisms of response activation, we asked subjects to respond differentially to the central letter of one of four arrays--HHHHH, SSHSS, SSSSS, and HHSHH--and measured event-related brain potentials (ERPs) and electromyographic activity (EMG). For very fast responses, accuracy was at chance level for all arrays, suggesting that subjects were guessing. For intermediate latency responses, accuracy was above chance if the noise was compatible with the targets and below chance if it was incompatible, suggesting that these responses were based on partial stimulus analysis. For slow responses, accuracy was above chance for all arrays, suggesting that these responses were based on complete stimulus analysis. The occurrence and accuracy of fast responses could be predicted by examining motor potentials preceding the presentation of the array. Measures of the motor potentials in the period following the presentation of the array suggested that partial analysis of stimulus information could activate responses and that the level of response activation at the time of the EMG response was constant for trials with different response latencies. The data are discussed in terms of a response channel conception.     

Unmasking the magnitude estimation response

The fuzzy judgement model of Ward (1979) predicts an inverse relation between the amount of stimulus information available to subjects and the magnitude of sequential dependencies on previous stimuli and responses in psychophysical scaling tasks. Ward confirmed this prediction for magnitude estimations of interdot distance for previous responses but not for previous stimuli, although the inverse relation has been repeatedly reported for both the previous stimuli and responses in absolute identification (e.g., Mori, 1989). This paper further explores this seemingly puzzling contradiction. A magnitude estimation of loudness experiment was conducted in which the amount of stimulus information available to subjects was manipulated by a modified version of informational masking (Watson, 1987). An absolute-identification-with-feedback experiment was also conducted to check the effectiveness of the informational masking in reducing the amount of stimulus information. The results of the magnitude estimation experiment show a striking similarity with those of Ward and generalize the failure of sequential dependencies on previous stimuli to vary inversely with stimulus information. An additional assumption that judgement strategies are altered under low-information conditions is necessary to explain this result.     

Visual attention and the temporal dynamics of feature integration

Two experiments studied the emergence of bindings between stimulus features (object files) and between stimulus and response features (event files) over time. Choice responses (R2) were signalled by the shape of a stimulus (S2) that followed another stimulus (S1) of the same or different shape, location, and colour. S1 did not require a response (Experiment 1) or trigger a precued simple response (R1) that was or was not repeated by R2 (Experiment 2). Results demonstrate that the mere cooccurrence of stimulus features, and of stimuli and responses, is sufficient to bind their codes. Bindings emerge quickly and remain intact for at least four seconds. Which features are considered depends on their task‐relevance; hence, integration reflects the current attentional set. There was no consistent trend toward higher order interactions as a function of time or of the amount of attention devoted to S1, suggesting that features are not integrated into a single, global superstructure, but enter independent local bindings presumably subserving different functions.     

S-R compatibility and response selection

In serial stage models, perception and action are usually thought to be linked to each other by an S-R translation mechanism. However, phenomena of S-R compatibility suggest a more direct relationship between perceptual and action domains. We discuss behavioral and psychophysiological evidence that irrelevant stimulus information automatically activates response codes, but then decays over time.

In a series of reaction time studies and electrophysiological experiments, we investigated both temporal and functional properties of the assumed automatic response activation process. We found that the amount of interference due to irrelevant spatial information depends upon how long its availability precedes that of the information relevant for response selection. This indicates that response activation decays rather quickly. If response-relevant and irrelevant spatial information are simultaneously available, electrophysiological measurements show that automatic activation of the spatially corresponding response rises soon after stimulus onset, but then dissipates and gets replaced by the activation of the response indicated by the relevant stimulus attribute.

We conclude that these findings do not support a pure translation account, but rather suggest the presence of two parallel and (at least partially) independent routes from perception to action: A direct route, allowing for automatic activation of response codes if stimulus and response features overlap, and an indirect route linking S and R codes in an arbitrary manner. Via the direct route responses may be primed independent of task-specific contingencies, while the correct response is selected via the indirect route. This use suggests that (a) the transmission of stimulus information to response stages does not (fully) depend on task relevance and that (b) different stimulus features can be transmitted asynchronously and independently from one another.     

The distribution of observing responses in a mixed FI-FR schedule,

In Exp I, three pigeons were trained on an observing response procedure where observing responses produced a stimulus correlated either with FI or with FR. Stimulus duration was 30 sec. During FR, the subjects completed the ratio before the stimulus terminated. During FI, the subjects usually observed the stimulus only once. Observing responses occurred immediately after food reinforcement. In Exp II, stimulus duration was shortened to 5 sec and the FR for food was increased. The results were similar to those of Exp 1. During most FIs and FRs, only one observing response occurred. The results of both experiments could be interpreted in a response competition framework. Immediately after food reinforcement, observing behavior is strong. When behavior on the food key begins it competes with further observing behavior.     

Discrete versus continuous stage models of human information processing: in search of partial output

This article introduces a new technique designed to study the flow of information through processing stages in choice reaction time tasks. The technique was designed to determine whether response preparation can begin before stimulus identification is complete ("continuous" models), or if a stimulus must be fully identified prior to any response activation ("discrete" models). To control the information available at various times during stimulus identification, some relevant stimulus characteristics were made easy to discriminate and some were made hard to discriminate. The experimental strategy was to look for effects of partial output based on information conveyed by characteristics that were easy to discriminate. The technique capitalized on the fact, demonstrated in Experiment 1, that preparation of two response fingers on the same hand is more effective than preparation of two response fingers on different hands. The usefulness of partial output was varied by manipulating the assignments of stimuli to responses. For some mappings partial information could contribute to effective response preparation because the responses consistent with partial information were assigned to fingers on the same hand. For other mappings partial information could not contribute to effective response preparation because the responses consistent with partial information were assigned to fingers of different hands. Performance differences between these mappings were considered evidence that partial information about a stimulus was transmitted to response activation processes before the stimulus was uniquely identified, and thus were considered evidence against discrete transmission of information about the stimulus as a whole. A variety of stimulus sets were studied; the results suggest that information is transmitted discretely with respect to stimulus codes, although distinct codes activated by a single stimulus may be transmitted at different times.     

The generation effect: Further tests of the lexical activation hypothesis

Three experiments compared recognition memory for word versus nonword responses when they had been either read or generated using a rhyme rule and either a word or nonword stimulus. That is, either the wordshop or the nonwordthop was generated from either the wordchop or the nonwordphop. In Experiment 1, the lexicality of the stimulus and response terms was manipulated orthogonally between subjects; in Experiments 2 and 3, it was manipulated orthogonally within subjects. In Experiment 3, subjects also made a lexical (word-nonword) decision about each response term after it had been read or generated. In all three experiments, memory performance was better for generated than read responses. This generation effect occurred only if the response term was a word, regardless of whether the stimulus term was a word or a nonword. These results are discussed in terms of the roles that lexical memory and response unitization play in the generation effect.     

Sequential effects in absolute judgments of loudness

The effects of preceding stimuli on the judgments of current stimuli were examined in a study using absolute judgments of loudness with feedback. It was found that the response on a given trial was dependent on the stimuli in the preceding sequence of at least five trials. Both assimilation and contrast effects were observed. The form of the dependency of a response on a prior stimulus was a function of the ordinal position of the stimulus in the preceding sequence of trials. The stimulus on the immediately preceding trial had an assimilative effect on the response and preceding stimuli two to five trials removed all showed a contrast effect on a given response. The extent to which these preceding stimuli contributed to the contrast effect was an increasing function of their recency. The reversal of the dependency of the response, from assimilation to the stimulus one trial back, to contrast with the stimuli two and more trials back, indicates a unique function of the immediately preceding stimulus in this task. Since there was a reduction in the variance of responses to those stimuli similar in value to the immediately preceding stimulus, it is proposed that the stimulus and feedback on the last trial were remembered and used asa standardin judging the presented stimulus. A model is presented in which it is assumed that the memory of the magnitude of the immediately preceding stimulus is contaminated in specified ways by prior stimuli in the series. The empirical findings of assimilation and contrastare expected consequences of the proposed memorial processes.     

Response preparation and stimulus-response congruence to fractionating reaction time of upper and lower limbs

We measured the fractionating reaction time for upper and lower limbs of 18 young men, using an electromyogram to clarify the interaction of response preparation and stimulus-response congruence on premotor and motor time. The reaction time was divided into two periods with respect to the onset of the electromyogram, premotor and motor components. Manipulating the probability of the Go versus NoGo signals varied three different amounts of response preparation. Prior to the imperative stimulus, precue information about the position of a stimulus was presented. In the stimulus-response congruent task, subjects were required to release a key on the same side of the body using either an upper or lower limb in response to an imperative Go stimulus. In the stimulus-response incongruent task, subjects were required to act in a reverse manner. Subjects were not supposed to respond to the NoGo stimulus. The premotor time of the upper and lower limb responses was affected by the respective effects of response preparation and stimulus-response congruence. The motor time of the upper and lower limb responses increased as the probability of the Go signal decreased but not in relation to stimulus-response congruence. These results suggest that response preparation affects not only information processing time but also peripheral motor activity due to motor programming, and that the stimulus-response congruence effect on motor time disappears when information about the position of the imperative stimulus is precued.     

Validity and boundary conditions of automatic response activation in the Simon task.

Three experiments were conducted to determine whether spatial stimulus-response compatibility effects are caused by automatic response activation by stimulus properties or by interference between codes during translation of stimulus into response coordinates. The main evidence against activation has been that in a Simon task with hands crossed, responses are faster at the response location ipsilateral to the stimulus though manipulated by the hand contralateral to the stimulus. The experiments were conducted with hands in standard and in crossed positions and electroencephalogram measures showed coactivation of the motor cortex induced by stimulus position primarily during standard hand positions with visual stimuli. Only in this condition did the Simon effect decay with longer response times. The visual Simon effect appeared to be due to specific mechanisms of visuomotor information transmission that are not responsible for the effects obtained with crossed hands or auditory stimuli.